Ventilator-Induced Lung Injury: Mechanotransduction and Potential Therapeutic Targets

He Ren , Ziqi Shang , Alastair G. Stewart , Ying-xin Qi , Kai Huang

MedComm ›› 2026, Vol. 7 ›› Issue (2) : e70598

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MedComm ›› 2026, Vol. 7 ›› Issue (2) :e70598 DOI: 10.1002/mco2.70598
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Ventilator-Induced Lung Injury: Mechanotransduction and Potential Therapeutic Targets
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Abstract

Mechanical ventilation (MV) serves as a critical intervention to maintain adequate gas exchange. Unfortunately, MV often leads to the development of ventilator-induced lung injury (VILI). VILI pathogenesis involves alveolar-capillary barrier disruption, dysregulated inflammation, and mechanotransduction-driven cellular dysfunction, but the interplay of these mechanisms remains incompletely understood. Here, we review the types of mechanical stress in VILI, key signaling pathways implicated in MV-induced lung injury, with particular emphasis on the impact of altered mechanical forces in VILI. Furthermore, we discuss the cell-specific mechanisms in VILI. We also delineate the intricate molecular mechanisms that orchestrate intercellular communication in VILI. In addition, we discuss the limitations of current clinical strategies, and the identification of novel drug targets with transformative potential for treatment of VILI. Moreover, we summarize the current and emerging therapeutic strategies and discuss the existing knowledge gaps and future directions for VILI prevention. By integrating mechanical mechanistic insights with translational perspectives, this review identifies novel biomarkers and potential therapeutics to mitigate VILI. Our synthesis not only advances the understanding of VILI pathophysiology but also provides a framework for precision medicine approaches in critical care, ultimately optimizing MV outcomes.

Keywords

inflammation / mechanical stress / reactive oxygen species / ventilator-induced lung injury

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He Ren, Ziqi Shang, Alastair G. Stewart, Ying-xin Qi, Kai Huang. Ventilator-Induced Lung Injury: Mechanotransduction and Potential Therapeutic Targets. MedComm, 2026, 7(2): e70598 DOI:10.1002/mco2.70598

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References

[1]

K. Walter, “Mechanical Ventilation,” JAMA 326, no. 14 (2021): 1452.

[2]

E. Fan, D. Brodie, and A. S. Slutsky, “Acute Respiratory Distress Syndrome,” JAMA 319, no. 7 (2018): 698.

[3]

A. Fogagnolo, F. Montanaro, L. Al-Husinat, et al., “Management of Intraoperative Mechanical Ventilation to Prevent Postoperative Complications After General Anesthesia: A Narrative Review,” Journal of Clinical Medicine 10, no. 12 (2021): 2656.

[4]

R. G. Brower, M. A. Matthay, A. Morris, D. Schoenfeld, B. Taylor Thompson, and A. Wheeler, “Ventilation With Lower Tidal Volumes as Compared With Traditional Tidal Volumes for Acute Lung Injury and the Acute Respiratory Distress Syndrome,” New England Journal of Medicine 342, no. 18 (2000): 1301–1308.

[5]

H. Banavasi, P. Nguyen, H. Osman, and A. Soubani, “Management of ARDS – What Works and What Does Not,” American Journal of the Medical Sciences 362, no. 1 (2020): 13–23.

[6]

R. G. Brower, M. A. Matthay, A. Morris, D. Schoenfeld, B. Taylor Thompson, and A. Wheeler, “Ventilation With Lower Tidal Volumes as Compared With Traditional Tidal Volumes for Acute Lung Injury and the Acute Respiratory Distress Syndrome,” New England Journal of Medicine 342, no. 18 (2000): 1301–1308.

[7]

T. Wang, C. Groß, A. A. Desai, et al., “Endothelial Cell Signaling and Ventilator-Induced Lung Injury: Molecular Mechanisms, Genomic Analyses, and Therapeutic Targets,” American Journal of Physiology-Lung Cellular and Molecular Physiology 312, no. 4 (2017): L452–L476.

[8]

M. A. Matthay, S. Bhattacharya, D. Gaver, et al., “Ventilator-Induced Lung Injury: In Vivo and In Vitro Mechanisms,” American Journal of Physiology-Lung Cellular and Molecular Physiology 283, no. 4 (2002): L678–L682.

[9]

M. J. Davis, S. Earley, Y.-S. Li, and S. Chien, “Vascular Mechanotransduction,” Physiological Reviews 103, no. 2 (2023): 1247–1421.

[10]

H. Ren, W. Hu, T. Jiang, Q. Yao, Y. Qi, and K. Huang, “Mechanical Stress Induced Mitochondrial Dysfunction in Cardiovascular Diseases: Novel Mechanisms and Therapeutic Targets,” Biomedicine & Pharmacotherapy 174 (2024): 116545.

[11]

X. Wang, Y. Shen, M. Shang, X. Liu, and L. L. Munn, “Endothelial Mechanobiology in Atherosclerosis,” Cardiovascular Research 119, no. 8 (2023): 1656–1675.

[12]

H. Bao, H.-P. Li, Q. Shi, et al., “Lamin A/c Negatively Regulated by MiR-124-3p Modulates Apoptosis of Vascular Smooth Muscle Cells During Cyclic Stretch Application in Rats,” Acta Physiologica 228, no. 3 (2019): e13374–e13474.

[13]

H. Bao, Y.-X. Chen, K. Huang, et al., “Platelet-Derived Microparticles Promote Endothelial Cell Proliferation in Hypertension via MiR-142–3p,” FASEB Journal 32, no. 7 (2018): 3912–3923.

[14]

K. Huang, H. Bao, Z.-Q. Yan, et al., “MicroRNA-33 Protects Against Neointimal Hyperplasia Induced by Arterial Mechanical Stretch in the Grafted Vein,” Cardiovascular Research 113, no. 5 (2017): 488–497.

[15]

G. Liu, B. B. Dong, S. Devanarayana, R.-C. Chen, and Q. Liu, “Emerging Roles of Mechanosensitive Ion Channels in Ventilator Induced Lung Injury: A Systematic Review,” Frontiers in Immunology 15 (2024): 1479230.

[16]

T. Jiang, Y. Zhang, Z. Guo, et al., “Mechanical Stress Induced NOX2 Promotes Endothelial Dysfunction in Ventilator-Induced Lung Injury: Potential Treatment With Quercetin,” Advanced Science 12, no. 28 (2025): e2502639.

[17]

A. M. Bilek, K. C. Dee, and D. P. Gaver, “Mechanisms of Surface-Tension-Induced Epithelial Cell Damage in a Model of Pulmonary Airway Reopening,” Journal of Applied Physiology 94, no. 2 (2003): 770–783.

[18]

S. Düring, K. Kuljit, N. K. J. Adhikari, et al., “Understanding Ventilator-Induced Lung Injury: The Role of Mechanical Power,” Journal of Critical Care 85, (2024): 154902.

[19]

G. Liu, B. B. Dong, S. Devanarayana, R.-C. Chen, and Q. Liu, “Emerging Roles of Mechanosensitive Ion Channels in Ventilator Induced Lung Injury: A Systematic Review,” Frontiers in Immunology 15 (2024): 1479230.

[20]

M. C. Bachmann, M. Benites, V. Oviedo, et al., “Association Between Controlled Mechanical Ventilation and Systemic Inflammation in Acute Hypoxemic Respiratory Failure: An Observational Cohort Study,” Critical Care 29, no. 1 (2025): 482.

[21]

M. C. J. Kneyber, R. P. Gazendam, H. W. M. Niessen, et al., “Mechanical Ventilation During Experimental Sepsis Increases Deposition of Advanced Glycation End Products and Myocardial Inflammation,” Critical Care 13, no. 3 (2009): R87.

[22]

J. L. Koyner and P. T. Murray, “Mechanical Ventilation and the Kidney,” Blood Purification 29, no. 1 (2010): 52–68.

[23]

M. Ziaka and A. Exadaktylos, “Gut-Derived Immune Cells and the Gut-Lung Axis in ARDS,” Critical Care 28, no. 1 (2024): 220.

[24]

M. Ziaka and A. Exadaktylos, “Brain–Lung Interactions and Mechanical Ventilation in Patients With Isolated Brain Injury,” Critical Care 25, no. 1 (2021): 358.

[25]

L. Knudsen and M. Ochs, “The Micromechanics of Lung Alveoli: Structure and Function of Surfactant and Tissue Components,” Histochemistry and Cell Biology 150, no. 6 (2018): 661–676.

[26]

J. K. Burgess and R. Gosens, “Mechanotransduction and the Extracellular Matrix: Key Drivers of Lung Pathologies and Drug Responsiveness,” Biochemical Pharmacology 228 (2024): 116255.

[27]

S. T. Torrino, E. M. Grasset, S. Audebert, et al., “Mechano-Induced Cell Metabolism Promotes Microtubule Glutamylation to Force Metastasis,” Cell Metabolism 33, no. 7 (2021): 1342–1357.

[28]

J. S. Park, C. J. Burckhardt, R. Lazcano, et al., “Mechanical Regulation of Glycolysis via Cytoskeleton Architecture,” Nature 578, no. 7796 (2020): 621–626.

[29]

K. Shiraishi, P. P. Shah, M. P. Morley, et al., “Biophysical Forces Mediated by Respiration Maintain Lung Alveolar Epithelial Cell Fate,” Cell 186, no. 7 (2023): 1478–1492.

[30]

P. Romani, N. Nirchio, M. Arboit, et al., “Mitochondrial Fission Links ECM Mechanotransduction to Metabolic Redox Homeostasis and Metastatic Chemotherapy Resistance,” Nature Cell Biology 24, no. 2 (2022): 168–180.

[31]

L. Ye, Q. Zeng, M. Ling, et al., “Inhibition of IP3R/Ca2+ Dysregulation Protects Mice From Ventilator-Induced Lung Injury via Endoplasmic Reticulum and Mitochondrial Pathways,” Frontiers in Immunology 12 (2021): 729094.

[32]

A. Gillich, F. Zhang, C. G. Farmer, et al., “Capillary Cell-Type Specialization in the Alveolus,” Nature 586, no. 7831 (2020): 785–789.

[33]

K. Hamanaka, M. Jian, D. S. Weber, et al., “TRPV4 Initiates the Acute Calcium-Dependent Permeability Increase During Ventilator-Induced Lung Injury in Isolated Mouse Lungs,” American Journal of Physiology-Lung Cellular and Molecular Physiology 293, no. 4 (2007): L923–L932.

[34]

S. C. Jurek, M. Hirano-Kobayashi, H. Chiang, D. S. Kohane, and B. D. Matthews, “Prevention of Ventilator-Induced Lung Edema by Inhalation of Nanoparticles Releasing Ruthenium Red,” American Journal of Respiratory Cell and Molecular Biology 50, no. 6 (2014): 1107–1117.

[35]

Q. Yu, D. Wang, X. Wen, et al., “Adipose-Derived Exosomes Protect the Pulmonary Endothelial Barrier in Ventilator-Induced Lung Injury by Inhibiting the TRPV4/Ca2+ Signaling Pathway,” American Journal of Physiology-Lung Cellular and Molecular Physiology 318, no. 4 (2020): L723–L741.

[36]

Q. Lu, E. A. Zemskov, X. Sun, et al., “Activation of the Mechanosensitive Ca2+ Channel TRPV4 Induces Endothelial Barrier Permeability via the Disruption of Mitochondrial Bioenergetics,” Redox Biology 38 (2021): 101785.

[37]

M. Zhong, W. Wu, H. Kang, et al., “Alveolar Stretch Activation of Endothelial Piezo1 Protects Adherens Junctions and Lung Vascular Barrier,” American Journal of Respiratory Cell and Molecular Biology 62, no. 2 (2019): 168–177.

[38]

L. Jiang, Y. Zhang, D. Lu, et al., “Mechanosensitive Piezo1 Channel Activation Promotes Ventilator-Induced Lung Injury via Disruption of Endothelial Junctions in ARDS Rats,” Biochemical and Biophysical Research Communications 556 (2021): 79–86.

[39]

J. Zhang, L. Jiang, T. Huang, et al., “Mechanosensitive Cation Channel Piezo1 Contributes to Ventilator-Induced Lung Injury by Activating RhoA/ROCK1 in Rats,” Research Square 22 (2021): 250.

[40]

A. Schwingshackl, “The Role of Stretch-Activated Ion Channels in Acute Respiratory Distress Syndrome: Finally a New Target?,” American Journal of Physiology-Lung Cellular and Molecular Physiology 311, no. 3 (2016): L639–L652.

[41]

G. Otulakowski, D. Engelberts, M. Post, C. Masterson, and B. P. Kavanagh, “Mechanical Ventilation Induces Desensitization of Lung Axl Tyrosine Kinase Receptors,” Anesthesiology 129, no. 1 (2018): 143–153.

[42]

X. Song, Y. Liu, L. Dong, and Y. Wang, “Stromal-Interacting Molecule 1 (Stim1)/Orai1 Modulates Endothelial Permeability in Ventilator-Induced Lung Injury,” Medical Science Monitor 24 (2018): 9413–9423.

[43]

Z. Sun, S. S. Guo, and R. Fässler, “Integrin-Mediated Mechanotransduction,” Journal of Cell Biology 215, no. 4 (2016): 445–456.

[44]

G. Su, M. Hodnett, N. Wu, et al., “Integrin Αvβ5 Regulates Lung Vascular Permeability and Pulmonary Endothelial Barrier Function,” American Journal of Respiratory Cell and Molecular Biology 36, no. 3 (2007): 377–386.

[45]

M. Antosova, D. Mokra, L. Pepucha, et al., “Physiology of Nitric Oxide in the Respiratory System,” Physiological Research 66, no. S2 (2017): S159–S172.

[46]

K. Takenaka, Y. Nishimura, T. Nishiuma, et al., “Ventilator-Induced Lung Injury Is Reduced in Transgenic Mice That Overexpress Endothelial Nitric Oxide Synthase,” American Journal of Physiology-Lung Cellular and Molecular Physiology 290, no. 6 (2006): L1078–L1086.

[47]

Y. Ju, X. Sun, G. Xu, Q. Tai, and W. Gao, “Annexin A1 Peptide Ac2-26 Mitigates Ventilator-Induced Lung Injury in Acute Respiratory Distress Syndrome Rats and Partly Depended on the Endothelial Nitric Oxide Synthase Pathway,” Acta Cirúrgica Brasileira 37, no. 12 (2022): e371203.

[48]

K. Vaporidi, R. C. Francis, K. D. Bloch, and W. M. Zapol, “Nitric Oxide Synthase 3 Contributes to Ventilator-Induced Lung Injury,” American Journal of Physiology-Lung Cellular and Molecular Physiology 299, no. 2 (2010): L150–L159.

[49]

M. Cansever, M. A. Akin, M. Akcakus, et al., “Effect of Parenterally L-Arginine Supplementation on the Respiratory Distress Syndrome in Preterm Newborns,” Journal of Maternal-Fetal & Neonatal Medicine 29, no. 14 (2015): 2248–2251.

[50]

Y. C. Luiking, M. Poeze, and N. E. Deutz, “Arginine Infusion in Patients With Septic Shock Increases Nitric Oxide Production Without Haemodynamic Instability,” Clinical Science 128, no. 1 (2014): 57–67.

[51]

N. Mitin, K. L. Rossman, and C. J. Der, “Signaling Interplay in Ras Superfamily Function,” Current Biology 15, no. 14 (2005): R563–R574.

[52]

K. Liu, Y.-F. Mao, J. Zheng, et al., “SC5b-9-Induced Pulmonary Microvascular Endothelial Hyperpermeability Participates in Ventilator-Induced Lung Injury,” Cell Biochemistry and Biophysics 67, no. 3 (2013): 1421–1431.

[53]

Y. Wang, T. T. Gao, D. F. Xu, et al., “Upregulation of Sphingosine Kinase 1 Contributes to Ventilator-Associated Lung Injury in a Two-Hit Model,” International Journal of Molecular Medicine 44, no. 6 (2019): 2077–2090.

[54]

A. A. Birukova, Y. Tian, A. Meliton, A. Leff, T. Wu, and K. G. Birukov, “Stimulation of Rho Signaling by Pathologic Mechanical Stretch Is a ‘Second Hit’ to Rho-Independent Lung Injury Induced by IL-6,” American Journal of Physiology-Lung Cellular and Molecular Physiology 302, no. 9 (2012): L965–L975.

[55]

A. A. Birukova, D. Adyshev, B. Gorshkov, G. M. Bokoch, K. G. Birukov, and A. D. Verin, “GEF-H1 Is Involved in Agonist-Induced Human Pulmonary Endothelial Barrier Dysfunction,” AJP Lung Cellular and Molecular Physiology 290, no. 3 (2006): L540–L548.

[56]

X. Tian, Y. Tian, N. Sarich, T. Wu, and A. A. Birukova, “Novel Role of Stathmin in Microtubule-Dependent Control of Endothelial Permeability,” FASEB Journal 26, no. 9 (2012): 3862–3874.

[57]

A. A. Birukova, P. Fu, J. Xing, B. Yakubov, I. Cokic, and K. G. Birukov, “Mechanotransduction by GEF-H1 as a Novel Mechanism of Ventilator-Induced Vascular Endothelial Permeability,” American Journal of Physiology-Lung Cellular and Molecular Physiology 298, no. 6 (2010): L837–L848.

[58]

C. Quesnel, S. Marchand-Adam, A. Fabre, et al., “Regulation of Hepatocyte Growth Factor Secretion by Fibroblasts in Patients With Acute Lung Injury,” American Journal of Physiology-Lung Cellular and Molecular Physiology 294, no. 2 (2008): L334–L343.

[59]

A. A. Birukova, N. Moldobaeva, J. Xing, and K. G. Birukov, “Magnitude-Dependent Effects of Cyclic Stretch on HGF- and VEGF-Induced Pulmonary Endothelial Remodeling and Barrier Regulation,” American Journal of Physiology-Lung Cellular and Molecular Physiology 295, no. 4 (2008): L612–L623.

[60]

X. Tian, Y. Tian, G. Gawlak, et al., “Asef Controls Vascular Endothelial Permeability and Barrier Recovery in the Lung,” Molecular Biology of the Cell 26, no. 4 (2015): 636–650.

[61]

A. A. Birukova, T. K. Zagranichnaya, P. Fu, et al., “Prostaglandins PGE2 and PGI2 Promote Endothelial Barrier Enhancement via PKA- and Epac1/Rap1-Dependent Rac Activation,” Experimental Cell Research 313, no. 11 (2007): 2504–2520.

[62]

A. A. Birukova, D. Burdette, N. Moldobaeva, J. Xing, P. Fu, and K. G. Birukov, “Rac GTPase Is a Hub for Protein Kinase A and Epac Signaling in Endothelial Barrier Protection by CAMP,” Microvascular Research 79, no. 2 (2010): 128–138.

[63]

Y. Wang, Y.-J. Liu, D.-F. Xu, et al., “DRD1 Downregulation Contributes to Mechanical Stretch-Induced Lung Endothelial Barrier Dysfunction,” Theranostics 11, no. 6 (2021): 2505–2521.

[64]

A. Meliton, F. Meng, Y. Tian, A. A. Shah, A. A. Birukova, and K. G. Birukov, “Role of Krev Interaction Trapped-1 in Prostacyclin-Induced Protection Against Lung Vascular Permeability Induced by Excessive Mechanical Forces and Thrombin Receptor Activating Peptide 6,” American Journal of Respiratory Cell and Molecular Biology 53, no. 6 (2015): 834–843.

[65]

Y. Ke, P. Karki, C.-O. Zhang, et al., “Mechanosensitive Rap1 Activation Promotes Barrier Function of Lung Vascular Endothelium Under Cyclic Stretch,” Molecular Biology of the Cell 30, no. 8 (2019): 959–974.

[66]

V. J. Thannickal and B. L. Fanburg, “Reactive Oxygen Species in Cell Signaling,” American Journal of Physiology-Lung Cellular and Molecular Physiology 279, no. 6 (2000): L1005–L1028.

[67]

Y. Zhang, P. Murugesan, K. Huang, and H. Cai, “NADPH Oxidases and Oxidase Crosstalk in Cardiovascular Diseases: Novel Therapeutic Targets,” Nature Reviews Cardiology 17, no. 3 (2019): 170–194.

[68]

M. Mittal, M. R. Siddiqui, K. Tran, S. P. Reddy, and A. B. Malik, “Reactive Oxygen Species in Inflammation and Tissue Injury,” Antioxidants & Redox Signaling 20, no. 7 (2014): 1126–1167.

[69]

M. T. Kuipers, T. van der Poll, M. J. Schultz, and C. W. Wieland, “Bench-To-Bedside Review: Damage-Associated Molecular Patterns in the Onset of Ventilator-Induced Lung Injury,” Critical Care 15, no. 6 (2011): 235.

[70]

Z. Feng, J.-W. Wang, Y. Wang, W.-W. Dong, and Z.-F. Xu, “Propofol Protects Lung Endothelial Barrier Function by Suppression of High-Mobility Group Box 1 (HMGB1) Release and Mitochondrial Oxidative Damage Catalyzed by HMGB1,” Medical Science Monitor 25 (2019): 3199–3211.

[71]

J. H. Song, J. B. Mascarenhas, S. Sammani, et al., “TLR4 Activation Induces Inflammatory Vascular Permeability via Dock1 Targeting and NOX4 Upregulation,” Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 1868, no. 12 (2022): 166562.

[72]

C. L. Kempf, S. Sammani, T. Bermudez, et al., “Critical Role for the Lung Endothelial Nonmuscle Myosin Light-Chain Kinase Isoform in the Severity of Inflammatory Murine Lung Injury,” Pulmonary Circulation 12, no. 2 (2022): e12061.

[73]

Y. Wang, C.-F. Xu, Y. J. Liu, et al., “Salidroside Attenuates Ventilation Induced Lung Injury via SIRT1-Dependent Inhibition of NLRP3 Inflammasome,” Cellular Physiology and Biochemistry 42, no. 1 (2017): 34–43.

[74]

H. Wang, X. Sun, Q. Lu, et al., “The Mitochondrial Redistribution of ENOS Is Involved in Lipopolysaccharide Induced Inflammasome Activation During Acute Lung Injury,” Redox Biology 41 (2021): 101878.

[75]

C. M. Gross, R. Rafikov, S. Kumar, et al., “Endothelial Nitric Oxide Synthase Deficient Mice Are Protected From Lipopolysaccharide Induced Acute Lung Injury,” PLoS ONE 10, no. 3 (2015): e0119918.

[76]

A. Surendran, C. F. Dewey, B. C. Low, and L. Tucker-Kellogg, “A Computational Model of Mutual Antagonism in the Mechano-Signaling Network of RhoA and Nitric Oxide,” BMC Molecular and Cell Biology 22, no. S1 (2021): 47.

[77]

M. Eto, C. Barandiér, L. Rathgeb, et al., “Thrombin Suppresses Endothelial Nitric Oxide Synthase and Upregulates Endothelin-Converting Enzyme-1 Expression by Distinct Pathways,” Circulation Research 89, no. 7 (2001): 583–590.

[78]

K. Chitaley and R. C. Webb, “Nitric Oxide Induces Dilation of Rat Aorta via Inhibition of Rho-Kinase Signaling,” Hypertension 39, no. 2 (2002): 438–442.

[79]

P. Ding, R. Yang, C. Li, et al., “Fibroblast Growth Factor 21 Attenuates Ventilator-Induced Lung Injury by Inhibiting the NLRP3/Caspase-1/GSDMD Pyroptotic Pathway,” Critical Care 27, no. 1 (2023): 196.

[80]

G. Liu, B. B. Dong, Z. H. Ding, C. Lan, C. J. Zhu, and Q. Liu, “Unphysiological Lung Strain Promotes Ventilation-Induced Lung Injury via Activation of the PECAM-1/Src/STAT3 Signaling Pathway,” Frontiers in Pharmacology 15 (2025): 1469783.

[81]

R. E. E. Abdulnour, X. Peng, J. H. Finigan, et al., “Mechanical Stress Activates Xanthine Oxidoreductase Through MAP Kinase-Dependent Pathways,” AJP Lung Cellular and Molecular Physiology 291, no. 3 (2006): L345–L353.

[82]

B. Park M. H. Hoon, I. S. Shin, et al., “Erythropoietin-Producing Hepatoma Receptor Tyrosine Kinase A2 Modulation Associates With Protective Effect of Prone Position in Ventilator-Induced Lung Injury,” American Journal of Respiratory Cell and Molecular Biology 58, no. 4 (2018): 519–529.

[83]

S. Fan, J. He, Y. Yang, and D. Wang, “Intermedin Reduces Oxidative Stress and Apoptosis in Ventilator-Induced Lung Injury via JAK2/STAT3,” Frontiers in Pharmacology 12 (2022): 817874.

[84]

H. Amatullah, T. Maron-Gutierrez, Y. Shan, et al., “Protective Function of DJ-1/PARK7 in Lipopolysaccharide and Ventilator-Induced Acute Lung Injury,” Redox Biology 38 (2021): 101796.

[85]

W. Jiang, J. Liu, J. Cui, et al., “Ferroptosis Plays a Crucial Role in Lung Cell Damage Caused by Ventilation Stretch,” Free Radical Biology and Medicine 209 (2023): 84–95.

[86]

J. Wu, Y. Liang, P. Fu, et al., “Sphingosine-1-Phosphate Receptor 3 Induces Endothelial Barrier Loss via ADAM10-Mediated Vascular Endothelial-Cadherin Cleavage,” International Journal of Molecular Sciences 24, no. 22 (2023): 16083.

[87]

A. E. Garcia-Flores, C. M. Gross, E. A. Zemskov, et al., “Loss of SOX18/CLAUDIN5 Disrupts the Pulmonary Endothelial Barrier in Ventilator-Induced Lung Injury,” Frontiers in Physiology 13 (2022): 1066515.

[88]

C.-F. Xu, Y.-J. Liu, Y. Wang, et al., “Downregulation of R-Spondin1 Contributes to Mechanical Stretch-Induced Lung Injury,” Critical Care Medicine 47, no. 7 (2019): e587–e596.

[89]

C. E. Barkauskas, M. J. Cronce, C. R. Rackley, et al., “Type 2 Alveolar Cells Are Stem Cells in Adult Lung,” Journal of Clinical Investigation 123, no. 7 (2013): 3025–3036.

[90]

N. Pairet, S. Mang, G. Fois, et al., “TRPV4 Inhibition Attenuates Stretch-Induced Inflammatory Cellular Responses and Lung Barrier Dysfunction During Mechanical Ventilation,” PLoS ONE 13, no. 4 (2018): e0196055.

[91]

X.-Z. Fang, M. Li, Y.-X. Wang, et al., “Mechanosensitive Ion Channel Piezo1 Mediates Mechanical Ventilation-Exacerbated ARDS-Associated Pulmonary Fibrosis,” Journal of Advanced Research 53 (2022): 175–186.

[92]

Y. Wang, X. Fang, Y. Yang, et al., “Death-Associated Protein Kinase 1 Promotes Alveolar Epithelial Cell Apoptosis and Ventilator-Induced Lung Injury Through P53 Pathway,” Shock 57, no. 1 (2021): 140–150.

[93]

H. Lee, Q. Fei, A. Streicher, et al., “MTORC1 Is a Mechanosensor That Regulates Surfactant Function and Lung Compliance During Ventilator-Induced Lung Injury,” JCI Insight 6, no. 14 (2021): e137708.

[94]

X. Ran, S. Müller, C. Brunssen, et al., “Modulation of the Hippo-YAP Pathway by Cyclic Stretch in Rat Type 2 Alveolar Epithelial Cells—A Proof-of-Concept Study,” Frontiers in Physiology 14 (2023): 1253810.

[95]

I. López-Alonso, J. Blázquez-Prieto, L. Amado-Rodríguez, et al., “Preventing Loss of Mechanosensation by the Nuclear Membranes of Alveolar Cells Reduces Lung Injury in Mice During Mechanical Ventilation,” Science Translational Medicine 10, no. 456 (2018): eaam7598.

[96]

P. S. Makena, V. K. Gorantla, M. C. Ghosh, et al., “Deletion of Apoptosis Signal–Regulating Kinase–1 Prevents Ventilator-Induced Lung Injury in Mice,” American Journal of Respiratory Cell and Molecular Biology 46, no. 4 (2012): 461–469.

[97]

P. S. Makena, V. K. Gorantla, M. C. Ghosh, et al., “Lung Injury Caused by High Tidal Volume Mechanical Ventilation and Hyperoxia Is Dependent on Oxidant-Mediated C-Jun NH2-Terminal Kinase Activation,” Journal of Applied Physiology 111, no. 5 (2011): 1467–1476.

[98]

Z. Chen, S. He, S. Lian, et al., “The Wnt/β-Catenin Pathway Regulates Inflammation and Apoptosis in Ventilator-Induced Lung Injury,” Bioscience Reports 43, no. 3 (2023): BSR20222429.

[99]

M. O. Hengartner, “The Biochemistry of Apoptosis,” Nature 407, no. 6805 (2000): 770–776.

[100]

N. A. Maniatis, V. Harokopos, A. Thanassopoulou, et al., “A Critical Role for Gelsolin in Ventilator-Induced Lung Injury,” American Journal of Respiratory Cell and Molecular Biology 41, no. 4 (2009): 426–432.

[101]

T. Dolinay, B. E. Himes, M. Shumyatcher, G. G. Lawrence, and S. S. Margulies, “Integrated Stress Response Mediates Epithelial Injury in Mechanical Ventilation,” American Journal of Respiratory Cell and Molecular Biology 57, no. 2 (2017): 193–203.

[102]

Y. Demay, J. Perochon, S. Szuplewski, B. Mignotte, and S. Gaumer, “The PERK Pathway Independently Triggers Apoptosis and a Rac1/Slpr/JNK/Dilp8 Signaling Favoring Tissue Homeostasis in a Chronic ER Stress Drosophila Model,” Cell Death & Disease 5, no. 10 (2014): e1452–e1452.

[103]

M. T. Kuipers, H. Aslami, J. R. Janczy, et al., “Ventilator-Induced Lung Injury Is Mediated by the NLRP3 Inflammasome,” Anesthesiology 116, no. 5 (2012): 1104–1115.

[104]

H. Liu, C. Gu, M. Liu, et al., “Ventilator-Induced Lung Injury Is Alleviated by Inhibiting NLRP3 Inflammasome Activation,” Molecular Immunology 111 (2019): 1–10.

[105]

H. Liu, C. Gu, M. Liu, G. Liu, and Y. Wang, “NEK7 Mediated Assembly and Activation of NLRP3 Inflammasome Downstream of Potassium Efflux in Ventilator-Induced Lung Injury,” Biochemical Pharmacology 177 (2020): 113998.

[106]

J. A. Frank, J.-F. Pittet, C. Wray, and M. A. Matthay, “Protection From Experimental Ventilator-Induced Acute Lung Injury by IL-1 Receptor Blockade,” Thorax 63 (2007): 147–153.

[107]

P.-E. Charles, P. Tissières, S. Barbar, et al., “Mild-Stretch Mechanical Ventilation Upregulates Toll-Like Receptor 2 and Sensitizes the Lung to Bacterial Lipopeptide,” Critical Care 15, no. 4 (2011): R181–R181.

[108]

Y. Shan, A. Akram, H. Amatullah, et al., “ATF3 Protects Pulmonary Resident Cells From Acute and Ventilator-Induced Lung Injury by Preventing Nrf2 Degradation,” Antioxidants and Redox Signaling 22, no. 8 (2015): 651–668.

[109]

T. Eckle, K. Brodsky, M. Bonney, et al., “HIF1A Reduces Acute Lung Injury by Optimizing Carbohydrate Metabolism in the Alveolar Epithelium,” PLoS Biology 11, no. 9 (2013): e1001665.

[110]

C. U. Vohwinkel, E. J. Coit, N. Burns, et al., “Targeting Alveolar-Specific Succinate Dehydrogenase A Attenuates Pulmonary Inflammation During Acute Lung Injury,” FASEB Journal 35, no. 4 (2021): e21468.

[111]

K. Wu, C. Li, J. Lv, et al., “FN14 Promotes Ventilator-Induced Lung Injury by Regulating Pyroptosis via the ANXA2/ERK1/2 Axis,” International Immunopharmacology 162 (2025): 114500.

[112]

H. Ou, J. Lin, L. Ji, et al., “Ferritinophagy Mediated by the AMPK/ULK1 Pathway Is Involved in Ferroptosis Subsequent to Ventilator-Induced Lung Injury,” Respiratory Research 25, no. 1 (2024): 440.

[113]

J. Lin, H. Ou, B. Luo, et al., “Capsaicin Mitigates Ventilator-Induced Lung Injury by Suppressing Ferroptosis and Maintaining Mitochondrial Redox Homeostasis Through SIRT3-Dependent Mechanisms,” Molecular Medicine 30, no. 1 (2024): 148.

[114]

S. Lamouille, J. Xu, and R. Derynck, “Molecular Mechanisms of Epithelial–Mesenchymal Transition,” Nature Reviews Molecular Cell Biology 15, no. 3 (2014): 178–196.

[115]

N. E. Cabrera-Benítez, M. Parotto, M. Post, et al., “Mechanical Stress Induces Lung Fibrosis by Epithelial–Mesenchymal Transition,” Critical Care Medicine 40, no. 2 (2012): 510–517.

[116]

C. Martin, L. Papazian, M.-J. Payan, P. Saux, and F. Gouin, “Pulmonary Fibrosis Correlates With Outcome in Adult Respiratory Distress Syndrome,” Chest 107, no. 1 (1995): 196–200.

[117]

L. F. Li, Y.-Y. Liu, K.-C. Kao, et al., “Mechanical Ventilation Augments Bleomycin-Induced Epithelial–Mesenchymal Transition Through the Src Pathway,” Laboratory Investigation 94, no. 9 (2014): 1017–1029.

[118]

A. Gunatilaka, S. Zhang, W. Shun, and A. G. Stewart, “Anti-Fibrotic Strategies and Pulmonary Fibrosis,” Advances in Pharmacology 98 (2023): 179–224.

[119]

L. F. Li, K. C. Kao, Y. Y. Liu, et al., “Nintedanib Reduces Ventilation-Augmented Bleomycin-Induced Epithelial-Mesenchymal Transition and Lung Fibrosis Through Suppression of the Src Pathway,” Journal of Cellular and Molecular Medicine 21, no. 11 (2017): 2937–2949.

[120]

A. K. Wheaton, M. Agarwal, S. Jia, and K. K. Kim, “Lung Epithelial Cell Focal Adhesion Kinase Signaling Inhibits Lung Injury and Fibrosis,” American Journal of Physiology-Lung Cellular and Molecular Physiology 312, no. 5 (2017): L722–L730.

[121]

M. Fang, S. Fan, X. Yao, et al., “Transfection of Sox11 Plasmid Alleviates Ventilator-Induced Lung Injury via Sox11 and FAK,” Biochemical and Biophysical Research Communications 512, no. 2 (2019): 182–188.

[122]

R. P. Marshall, P. Gohlke, R. C. Chambers, et al., “Angiotensin II and the Fibroproliferative Response to Acute Lung Injury,” American Journal of Physiology-Lung Cellular and Molecular Physiology 286, no. 1 (2004): L156–L164.

[123]

J. Feng, X. Huang, Q. Xu, et al., “Pharmacological Inhibition of the ACE/Ang-2/AT1 Axis Alleviates Mechanical Ventilation-Induced Pulmonary Fibrosis,” International Immunopharmacology 131 (2024): 111855.

[124]

R. Zhang, Y. Pan, V. Fanelli, et al., “Mechanical Stress and the Induction of Lung Fibrosis via the Midkine Signaling Pathway,” American Journal of Respiratory and Critical Care Medicine 192, no. 3 (2015): 315–323.

[125]

L. F. Li, P. H. Chu, and C. Y. Hung, “Lumican Regulates Ventilation-Induced Epithelial-Mesenchymal Transition Through Extracelluar Signal-Regulated Kinase Pathway,” Chest 143, no. 5 (2013): 1252–1260.

[126]

N. Oikonomou, M. A. Mouratis, A. Tzouvelekis, et al., “Pulmonary Autotaxin Expression Contributes to the Pathogenesis of Pulmonary Fibrosis,” American Journal of Respiratory Cell and Molecular Biology 47, no. 5 (2012): 566–574.

[127]

I. Nikitopoulou, I. Ninou, N. Manitsopoulos, et al., “A Role for Bronchial Epithelial Autotaxin in Ventilator-Induced Lung Injury,” Intensive Care Medicine Experimental 9, no. 1 (2021): 12.

[128]

M. A. Matthay, “Resolution of Pulmonary Edema. Thirty Years of Progress,” American Journal of Respiratory and Critical Care Medicine 189, no. 11 (2014): 1301–1308.

[129]

Y. Adir, L. C. Welch, V. Dumasius, P. Factor, J. I. Sznajder, and K. M. Ridge, “Overexpression of the Na-K-ATPase α2-Subunit Improves Lung Liquid Clearance During Ventilation-Induced Lung Injury,” American Journal of Physiology-Lung Cellular and Molecular Physiology 294, no. 6 (2008): L1233–L1237.

[130]

F. J. Saldías, A. P. Comellas, L. Pesce, E. Lecuona, and J. I. Sznajder, “Dopamine Increases Lung Liquid Clearance During Mechanical Ventilation,” American Journal of Physiology-Lung Cellular and Molecular Physiology 283, no. 1 (2002): L136–L143.

[131]

J. Goerke, “Pulmonary Surfactant: Functions and Molecular Composition,” Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 1408, no. 2–3 (1998): 79–89.

[132]

S. Milos, R. Khazaee, L. A. McCaig, et al., “Impact of Ventilation-Induced Lung Injury on the Structure and Function of Lamellar Bodies,” American Journal of Physiology-Lung Cellular and Molecular Physiology 313, no. 3 (2017): L524–L533.

[133]

A. N. Rizzo, S. M. Haeger, K. Oshima, et al., “Alveolar Epithelial Glycocalyx Degradation Mediates Surfactant Dysfunction and Contributes to Acute Respiratory Distress Syndrome,” JCI Insight 7, no. 2 (2022): e154573.

[134]

M. Liu, C. Gu, and Y. Wang, “Upregulation of the Tight Junction Protein Occludin: Effects on Ventilation-Induced Lung Injury and Mechanisms of Action,” BMC Pulmonary Medicine 14, no. 1 (2014): 94.

[135]

Z. Tao, Y. Jie, Z. Mingru, et al., “The Elk1/MMP-9 Axis Regulates E-Cadherin and Occludin in Ventilator-Induced Lung Injury,” Respiratory Research 22, no. 1 (2021): 233.

[136]

V. Suryadevara, P. Fu, D. Ebenezer, et al., “Sphingolipids in Ventilator Induced Lung Injury: Role of Sphingosine-1-Phosphate Lyase,” International Journal of Molecular Sciences 19, no. 1 (2018): 114.

[137]

L. Guillot, N. Nathan, O. Tabary, et al., “Alveolar Epithelial Cells: Master Regulators of Lung Homeostasis,” International Journal of Biochemistry & Cell Biology 45, no. 11 (2013): 2568–2573.

[138]

S. Shurbaji, I. M. El-Sherbiny, M. Alser, et al., “Nitric Oxide Releasing Hydrogel Nanoparticles Decreases Epithelial Cell Injuries Associated With Airway Reopening,” Frontiers in Bioengineering and Biotechnology 8 (2021): 579788.

[139]

C. Schwayer, S. Shamipour, K. Pranjic-Ferscha, et al., “Mechanosensation of Tight Junctions Depends on ZO-1 Phase Separation and Flow,” Cell 179, no. 4 (2019): 937–952.

[140]

H. Liu, X. Yang, and G. Liu, “Regulation of Cell Proliferation and Transdifferentiation Compensates for Ventilator-Induced Lung Injury Mediated by NLRP3 Inflammasome Activation,” Immunity, Inflammation and Disease 11, no. 10 (2023): e1062.

[141]

K. W. Gibbs, M. W. Semler, B. E. Driver, et al., “Noninvasive Ventilation for Preoxygenation During Emergency Intubation,” New England Journal of Medicine 390, no. 23 (2024): 2165–2177.

[142]

T. A. Lilien, M. J. S. David, J. Bos, and R. A. Bem, “Hyperoxia-Induced Lung Injury in Acute Respiratory Distress Syndrome: What Is Its Relative Impact?,” American Journal of Physiology-Lung Cellular and Molecular Physiology 325, no. 1 (2023): L9–L16.

[143]

J. I. Gray and D. L. Farber, “Tissue-Resident Immune Cells in Humans,” Annual Review of Immunology 40, no. 1 (2022): 195–220.

[144]

D. Liu, Z. Yan, R. D. Minshall, D. E. Schwartz, Y. Chen, and G. Hu, “Activation of Calpains Mediates Early Lung Neutrophilic Inflammation in Ventilator-Induced Lung Injury,” American Journal of Physiology-Lung Cellular and Molecular Physiology 302, no. 4 (2012): L370–L379.

[145]

W. Karzai, X. Cui, N. Heinicke, et al., “Neutrophil Stimulation With Granulocyte Colony-Stimulating Factor Worsens Ventilator-Induced Lung Injury and Mortality in Rats,” Anesthesiology 103, no. 5 (2005): 996–1005.

[146]

H. Zhang, G. P. Downey, P. M. Suter, A. S. Slutsky, and V. Marco Ranieri, “Conventional Mechanical Ventilation Is Associated With Bronchoalveolar Lavage-Induced Activation of Polymorphonuclear Leukocytes,” Anesthesiology 97, no. 6 (2002): 1426–1433.

[147]

S. Choudhury, M. R. Wilson, M. E. Goddard, K. P. O'Dea, and M. Takata, “Mechanisms of Early Pulmonary Neutrophil Sequestration in Ventilator-Induced Lung Injury in Mice,” American Journal of Physiology-Lung Cellular and Molecular Physiology 287, no. 5 (2004): L902–L910.

[148]

S. Gil, A. W. Farnand, W. A. Altemeier, et al., “Fas-Deficient Mice Have Impaired Alveolar Neutrophil Recruitment and Decreased Expression of Anti-KC Autoantibody:KC Complexes in a Model of Acute Lung Injury,” Respiratory Research 13, no. 1 (2012): 91–91.

[149]

J. H. Kim, M. H. Suk, D. W. Yoon, et al., “Inhibition of Matrix Metalloproteinase-9 Prevents Neutrophilic Inflammation in Ventilator-Induced Lung Injury,” American Journal of Physiology-Lung Cellular and Molecular Physiology 291, no. 4 (2006): L580–L587.

[150]

A. M. Kaynar, A. McGarry Houghton, E. H. Lum, B. R. Pitt, and S. D. Shapiro, “Neutrophil Elastase Is Needed for Neutrophil Emigration Into Lungs in Ventilator-Induced Lung Injury,” American Journal of Respiratory Cell and Molecular Biology 39, no. 1 (2008): 53–60.

[151]

A. Mishra, Y. Guo, L. Zhang, et al., “A Critical Role for P2×7 Receptor–Induced VCAM-1 Shedding and Neutrophil Infiltration During Acute Lung Injury,” Journal of Immunology 197, no. 7 (2016): 2828–2837.

[152]

E. K. Wolthuis, J.-J. H. H. Alexander, V. W. Joris, N. P. Juffermans, and M. J. Schultz, “Plasminogen Activator Inhibitor-Type I Gene Deficient Mice Show Reduced Influx of Neutrophils in Ventilator-Induced Lung Injury,” Critical Care Research and Practice 2011 (2011): 1–11.

[153]

V. Mirakaj, C. A. Thix, S. Laucher, et al., “Netrin-1 Dampens Pulmonary Inflammation During Acute Lung Injury,” American Journal of Respiratory and Critical Care Medicine 181, no. 8 (2010): 815–824.

[154]

V. Brinkmann, U. Reichard, C. Goosmann, et al., “Neutrophil Extracellular Traps Kill Bacteria,” Science 303, no. 5663 (2004): 1532–1535.

[155]

F. Wartha, K. Beiter, S. Normark, and B. Henriques-Normark, “Neutrophil Extracellular Traps: Casting the NET Over Pathogenesis,” Current Opinion in Microbiology 10, no. 1 (2007): 52–56.

[156]

C. Yildiz, N. Palaniyar, G. Otulakowski, et al., “Mechanical Ventilation Induces Neutrophil Extracellular Trap Formation,” Anesthesiology 122, no. 4 (2015): 864–875.

[157]

N. Ding, F. Wang, H. Xiao, L. Xu, and S. She, “Mechanical Ventilation Enhances HMGB1 Expression in an LPS-Induced Lung Injury Model,” PLoS ONE 8, no. 9 (2013): e74633.

[158]

M. T. Kuipers, T. Vogl, H. Aslami, et al., “High Levels of S100A8/A9 Proteins Aggravate Ventilator-Induced Lung Injury via TLR4 Signaling,” PLoS ONE 8, no. 7 (2013): e68694.

[159]

H. Li, P. Pan, X. Su, et al., “Neutrophil Extracellular Traps Are Pathogenic in Ventilator-Induced Lung Injury and Partially Dependent on TLR4,” BioMed Research International 2017 (2017): 1–13.

[160]

K. Timmermans, S. Ei van der Wal, M. Vaneker, et al., “IL-1β Processing in Mechanical Ventilation-Induced Inflammation Is Dependent on Neutrophil Factors Rather Than Caspase-1,” Intensive Care Medicine Experimental 1, no. 1 (2013): 27.

[161]

X. Liao, W. Zhang, H. Dai, et al., “Neutrophil-Derived IL-17 Promotes Ventilator-Induced Lung Injury via P38 MAPK/MCP-1 Pathway Activation,” Frontiers in Immunology 12 (2021): 768813.

[162]

P. J. Wolters, C. Wray, R. E. Sutherland, et al., “Neutrophil-Derived IL-6 Limits Alveolar Barrier Disruption in Experimental Ventilator-Induced Lung Injury,” Journal of Immunology 182, no. 12 (2009): 8056–8062.

[163]

F. Geissmann, M. G. Manz, S. Jung, M. H. Sieweke, M. Merad, and K. Ley, “Development of Monocytes, Macrophages, and Dendritic Cells,” Science 327, no. 5966 (2010): 656–661.

[164]

M. R. Wilson, K. P. O'Dea, D. Zhang, A. D. Shearman, N. Rooijen, and M. Takata, “Role of Lung-Marginated Monocytes in an In Vivo Mouse Model of Ventilator-Induced Lung Injury,” American Journal of Respiratory and Critical Care Medicine 179, no. 10 (2009): 914–922.

[165]

T.-H. Huang, P.-H. Fang, J.-M. Li, H.-Y. Ling, C.-M. Lin, and C.-S. Shi, “Cyclooxygenase-2 Activity Regulates Recruitment of VEGF-Secreting Ly6Chigh Monocytes in Ventilator-Induced Lung Injury,” International Journal of Molecular Sciences 20, no. 7 (2019): 1771.

[166]

W. Zhang, H. Dai, F. Lin, et al., “Ly-6Chigh Inflammatory-Monocyte Recruitment Is Regulated by P38 MAPK/MCP-1 Activation and Promotes Ventilator-Induced Lung Injury,” International Immunopharmacology 78 (2020): 106015.

[167]

C.-S. Shi, T.-H. Huang, C.-K. Lin, et al., “VEGF Production by Ly6C+High Monocytes Contributes to Ventilator-Induced Lung Injury,” PLoS ONE 11, no. 10 (2016): e0165317.

[168]

C. Shi and E. G. Pamer, “Monocyte Recruitment During Infection and Inflammation,” Nature Reviews Immunology 11, no. 11 (2011): 762–774.

[169]

N. Joshi, J. M. Walter, and A. V. Misharin, “Alveolar Macrophages,” Cellular Immunology 330, no. 330 (2018): 86–90.

[170]

L. Bitker, N. Costes, D. L. Bars, et al., “Noninvasive Quantification of Macrophagic Lung Recruitment During Experimental Ventilation-Induced Lung Injury,” Journal of Applied Physiology 127, no. 2 (2019): 546–558.

[171]

F. G. Eyal, C. R. Hamm, and J. C. Parker, “Reduction in Alveolar Macrophages Attenuates Acute Ventilator Induced Lung Injury in Rats,” Intensive Care Medicine 33, no. 7 (2007): 1212–1218.

[172]

K. Hamanaka, M. Jian, M. I. Townsley, et al., “TRPV4 Channels Augment Macrophage Activation and Ventilator-Induced Lung Injury,” American Journal of Physiology-Lung Cellular and Molecular Physiology 299, no. 3 (2010): L353–L362.

[173]

Q. Luo, J. Luo, and Y. Wang, “YAP Deficiency Attenuates Pulmonary Injury Following Mechanical Ventilation Through the Regulation of M1/M2 Macrophage Polarization,” Journal of Inflammation Research 13 (2020): 1279–1290.

[174]

C. M. Bobba, Q. Fei, V. Shukla, et al., “Nanoparticle Delivery of MicroRNA-146a Regulates Mechanotransduction in Lung Macrophages and Mitigates Injury During Mechanical Ventilation,” Nature Communications 12, no. 1 (2021): 289.

[175]

H. Dai, L. Pan, F. Lin, W. Ge, W. Li, and S. He, “Mechanical Ventilation Modulates Toll-Like Receptors 2, 4, and 9 on Alveolar Macrophages in a Ventilator-Induced Lung Injury Model,” Journal of Thoracic Disease 7, no. 4 (2015): 616.

[176]

Z. Yu, T. Wang, L. Zhang, X. Yang, Q. Li, and X. Ding, “WISP1 and TLR4 on Macrophages Contribute to Ventilator-Induced Lung Injury,” Inflammation 43, no. 2 (2020): 425–432.

[177]

J. Wu, Z. Yan, D. E. Schwartz, J. Yu, A. B. Malik, and G. Hu, “Activation of NLRP3 Inflammasome in Alveolar Macrophages Contributes to Mechanical Stretch-Induced Lung Inflammation and Injury,” Journal of Immunology 190, no. 7 (2013): 3590–3599.

[178]

Y. Zhang, G. Liu, R. O. Dull, D. E. Schwartz, and G. Hu, “Autophagy in Pulmonary Macrophages Mediates Lung Inflammatory Injury via NLRP3 Inflammasome Activation During Mechanical Ventilation,” AJP Lung Cellular and Molecular Physiology 307, no. 2 (2014): L173–L185.

[179]

M. Dai, Q. Li, and P. Pan, “The Modulation of Interferon Regulatory Factor-1 via Caspase-1-Mediated Alveolar Macrophage Pyroptosis in Ventilator-Induced Lung Injury,” Mediators of Inflammation 2022 (2022): 1–12.

[180]

J. Tong, X.-D. Zhou, V. P. Kolosov, and J. M. Perelman, “Role of the JNK Pathway on the Expression of Inflammatory Factors in Alveolar Macrophages Under Mechanical Ventilation,” International Immunopharmacology 17, no. 3 (2013): 821–827.

[181]

Y. Shiga, R. Sugamata, C. Iwamura, et al., “Effect of Invariant Natural Killer T Cells With IL-5 and Activated IL-6 Receptor in Ventilator-Associated Lung Injury in Mice,” Experimental Lung Research 40, no. 1 (2013): 1–11.

[182]

D. L. Norton, A. Ceppe, M. K. Tune, et al., “Bronchoalveolar Tregs Are Associated With Duration of Mechanical Ventilation in Acute Respiratory Distress Syndrome,” Journal of Translational Medicine 18, no. 1 (2020): 427.

[183]

J. C. Worrell and M. K. L. MacLeod, “Stromal–Immune Cell Crosstalk Fundamentally Alters the Lung Microenvironment Following Tissue Insult,” Immunology 163, no. 3 (2021): 239–249.

[184]

E. A. Hines and X. Sun, “Tissue Crosstalk in Lung Development,” Journal of Cellular Biochemistry 115, no. 9 (2014): 1469–1477.

[185]

L. Song, K. Li, H. Chen, and L. Xie, “Cell Crosstalk in Alveolar Microenvironment: From Lung Injury to Fibrosis,” American Journal of Respiratory Cell and Molecular Biology 71, no. 1 (2024): 30–42.

[186]

J. Creighton, “Factors Controlling Vascular Permeability: Transmitting Mechanical Signals. Focus on 'Mechanical Induction of Group v Phospholipase A2 Causes Lung Inflammation and Acute Lung Injury,” American Journal of Physiology-Lung Cellular and Molecular Physiology 305, no. 4 (2013): L279–L281.

[187]

L.-F. Li, S.-K. Liao, C.-H. Lee, C.-C. Huang, and D. A. Quinn, “Involvement of Akt and Endothelial Nitric Oxide Synthase in Ventilation-Induced Neutrophil Infiltration: A Prospective, Controlled Animal Experiment,” Critical Care 11, no. 4 (2007): R89.

[188]

M. Koeppen, E. N. McNamee, K. S. Brodsky, et al., “Detrimental Role of the Airway Mucin Muc5ac During Ventilator-Induced Lung Injury,” Mucosal Immunology 6, no. 4 (2013): 762–775.

[189]

S. M. Kreda, L. Seminario-Vidal, C. A. Heusden, et al., “Receptor-Promoted Exocytosis of Airway Epithelial Mucin Granules Containing a Spectrum of Adenine Nucleotides,” Journal of Physiology 588, no. Pt 12 (2010): 2255–2267.

[190]

H. Matsuyama, F. Amaya, S. Hashimoto, et al., “Acute Lung Inflammation and Ventilator-Induced Lung Injury Caused by ATP via the P2Y Receptors: An Experimental Study,” Respiratory Research 9, no. 1 (2008): 79.

[191]

M. W. Koh, R. F. Baldi, S. Soni, et al., “Secreted Extracellular Cyclophilin a Is a Novel Mediator of Ventilator-Induced Lung Injury,” American Journal of Respiratory and Critical Care Medicine 204, no. 4 (2021): 421–430.

[192]

Y. Wang, W. Xie, Y. Feng, et al., “Epithelial-Derived Exosomes Promote M2 Macrophage Polarization via Notch2/SOCS1 During Mechanical Ventilation,” International Journal of Molecular Medicine 50, no. 1 (2022): 96.

[193]

J. A. Frank, C. M. Wray, D. F. McAuley, R. Schwendener, and M. A. Matthay, “Alveolar Macrophages Contribute to Alveolar Barrier Dysfunction in Ventilator-Induced Lung Injury,” American Journal of Physiology-Lung Cellular and Molecular Physiology 291, no. 6 (2006): L1191–L1198.

[194]

H. Han, Q. Xie, R. Shao, J. Li, and X. Du, “Alveolar Macrophage-Derived GVPLA2 Promotes Ventilator-Induced Lung Injury via the CPLA2/PGE2 Pathway,” BMC Pulmonary Medicine 23, no. 1 (2023): 494.

[195]

L.-F. Li, Y.-T. Lai, C.-H. Chang, et al., “Neutrophil Elastase Inhibitor Reduces Ventilation-Induced Lung Injury via Nuclear Factor-ΚB and NF-ΚB Repressing Factor in Mice,” Experimental Biology and Medicine 239, no. 8 (2014): 1045–1057.

[196]

J. Zheng, Y. Huang, D. Islam, et al., “Dual Effects of Human Neutrophil Peptides in a Mouse Model of Pneumonia and Ventilator-Induced Lung Injury,” Respiratory Research 19, no. 1 (2018): 190.

[197]

L. Wang, Y. Zhang, N. Zhang, J. Xia, Q. Zhan, and C. Wang, “Potential Role of M2 Macrophage Polarization in Ventilator-Induced Lung Fibrosis,” International Immunopharmacology 75 (2019): 105795.

[198]

V. Neudecker, K. S. Brodsky, E. T. Clambey, et al., “Neutrophil Transfer of MiR-223 to Lung Epithelial Cells Dampens Acute Lung Injury in Mice,” Science Translational Medicine 9, no. 408 (2017): eaah5360.

[199]

R. Ma, P. Wu, Q. Shi, D. Song, and H. Fang, “Telocytes Promote VEGF Expression and Alleviate Ventilator-Induced Lung Injury in Mice,” Acta Biochimica et Biophysica Sinica 50, no. 8 (2018): 817–825.

[200]

M. T. Yiming, D. J. Lederer, L. Sun, A. Huertas, A. C. Issekutz, and S. Bhattacharya, “Platelets Enhance Endothelial Adhesiveness in High Tidal Volume Ventilation,” American Journal of Respiratory Cell and Molecular Biology 39, no. 5 (2008): 569–575.

[201]

M. Ziaka and A. Exadaktylos, “Brain–Lung Interactions and Mechanical Ventilation in Patients With Isolated Brain Injury,” Critical Care 25, no. 1 (2021): 358.

[202]

M. R. Grübler, O. Wigger, D. Berger, and S. Blöchlinger, “Basic Concepts of Heart-Lung Interactions During Mechanical Ventilation,” Swiss Medical Weekly 147, no. 3738 (2017): w14491.

[203]

M. Hepokoski, J. A. Englert, R. M. Baron, et al., “Ventilator-Induced Lung Injury Increases Expression of Endothelial Inflammatory Mediators in the Kidney,” American Journal of Physiology-Renal Physiology 312, no. 4 (2017): F654–F660.

[204]

M. Kredel, R. M. Muellenbach, R. W. Brock, et al., “Liver Dysfunction After Lung Recruitment Manoeuvres During Pressure-Controlled Ventilation in Experimental Acute Respiratory Distress,” Critical Care 11, no. 1 (2007): R13.

[205]

A. K. Ak and F. Anjum, Ventilator-Induced Lung Injury (VILI) (StatPearls Publishing, 2023).

[206]

M. A. Matthay, Y. Arabi, A. C. Arroliga, et al., “A New Global Definition of Acute Respiratory Distress Syndrome,” American Journal of Respiratory and Critical Care Medicine 209, no. 1 (2024): 37–47.

[207]

K. D. Wick, D. F. McAuley, J. E. Levitt, et al., “Promises and Challenges of Personalized Medicine to Guide ARDS Therapy,” Critical Care 25, no. 1 (2021): 404.

[208]

A. Pesenti, C. S. Calfee, L. Camporota, et al., “ESICM Guidelines on Acute Respiratory Distress Syndrome: Definition, Phenotyping and Respiratory Support Strategies,” Intensive Care Medicine 49, no. 1 (2023): 727–759.

[209]

N. Qadir, S. K. Sahetya, L. Munshi, et al., “An Update on Management of Adult Patients With Acute Respiratory Distress Syndrome: An Official American Thoracic Society Clinical Practice Guideline,” American Journal of Respiratory and Critical Care Medicine 209, no. 1 (2024): 24–36.

[210]

S. Tasaka, S. Ohshimo, M. Takeuchi, et al., “ARDS Clinical Practice Guideline 2021,” Respiratory Investigation 60, no. 4 (2022): 446–495.

[211]

R. Paudel, C. A. Trinkle, C. L. Waters, et al., “Mechanical Power: A New Concept in Mechanical Ventilation,” American Journal of the Medical Sciences 362, no. 6 (2021): 537–445.

[212]

E. Fan, D. Brodie, and A. S. Slutsky, “Acute Respiratory Distress Syndrome,” JAMA 319, no. 7 (2018): 698.

[213]

H. Liu, X. Yang, F. Qi, et al., “YAP Activity Protects Against Ventilator-Induced Lung Injury,” Frontiers in Physiology 16 (2025): 1578901.

[214]

L. Chimenti, T. Luque, M. R. Bonsignore, J. Ramírez, D. Navajas, and R. Farré, “Pre-Treatment With Mesenchymal Stem Cells Reduces Ventilator-Induced Lung Injury,” European Respiratory Journal 40, no. 4 (2012): 939–948.

[215]

Y. N. Ju, Y. J. Geng, X. T. Wang, J. Gong, J. Zhu, and W. Gao, “Endothelial Progenitor Cells Attenuate Ventilator-Induced Lung Injury With Large-Volume Ventilation,” Cell Transplantation 28, no. 12 (2019): 1674–1685.

[216]

K. Moriyama, A. Ishizaka, M. Nakamura, et al., “Enhancement of the Endotoxin Recognition Pathway by Ventilation With a Large Tidal Volume in Rabbits,” American Journal of Physiology-Lung Cellular and Molecular Physiology 286, no. 6 (2004): L1114–L1121.

[217]

E. D. Morrell, S. Grazioli, C. Hung, et al., “Alveolar CCN1 Is Associated With Mechanical Stretch and Acute Respiratory Distress Syndrome Severity,” American Journal of Physiology-Lung Cellular and Molecular Physiology 319, no. 5 (2020): L825–L832.

[218]

J. Villar, M. Muros, N. E. Cabrera-Benítez, et al., “Soluble Platelet-Endothelial Cell Adhesion Molecule-1, a Biomarker of Ventilator-Induced Lung Injury,” Critical Care 18, no. 2 (2014): R41.

[219]

R. Xiao and R. Chen, “Neutrophil Gelatinase-Associated Lipocalin as a Potential Novel Biomarker for Ventilator-Associated Lung Injury,” Molecular Medicine Reports 15, no. 6 (2017): 3535–3540.

[220]

L. M. Müller-Wirtz, D. Kiefer, F. Maurer, et al., “Volutrauma Increases Exhaled Pentanal in Rats: A Potential Breath Biomarker for Ventilator-Induced Lung Injury,” Anesthesia & Analgesia 133, no. 1 (2021): 263–273.

[221]

Y. Xie, H. Zheng, Z. Mou, Y. Wang, and X. Li, “High Expression of CXCL10/CXCR3 in Ventilator-Induced Lung Injury Caused by High Mechanical Power,” BioMed Research International 2022 (2022): 1–9.

[222]

J. A. Kropski, R. D. Fremont, C. S. Calfee, and L. B. Ware, “Clara Cell Protein (CC16), a Marker of Lung Epithelial Injury, Is Decreased in Plasma and Pulmonary Edema Fluid From Patients With Acute Lung Injury,” Chest 135, no. 6 (2009): 1440–1447.

[223]

S. Hoegl, K. A. Boost, H. Czerwonka, et al., “Inhaled IL-10 Reduces Biotrauma and Mortality in a Model of Ventilator-Induced Lung Injury,” Respiratory Medicine 103, no. 3 (2008): 463–470.

[224]

Y. Yang, L. Hu, H. Xia, et al., “Resolvin D1 Attenuates Mechanical Stretch-Induced Pulmonary Fibrosis via Epithelial-Mesenchymal Transition,” AJP Lung Cellular and Molecular Physiology 316, no. 6 (2019): L1013–L1024.

[225]

N. Nagre, X. Cong, H.-L. Ji, et al., “Inhaled TRIM72 Protein Protects Ventilation Injury to the Lung Through Injury-Guided Cell Repair,” American Journal of Respiratory Cell and Molecular Biology 59, no. 5 (2018): 635–647.

[226]

J. A. Robertson, D. Sauer, J. A. Gold, and S. A. Nonas, “The Role of Cyclooxygenase-2 in Mechanical Ventilation–Induced Lung Injury,” American Journal of Respiratory Cell and Molecular Biology 47, no. 3 (2012): 387–394.

[227]

E. N. Ogawa, A. Ishizaka, S. Tasaka, et al., “Contribution of High-Mobility Group Box-1 to the Development of Ventilator-Induced Lung Injury,” American Journal of Respiratory and Critical Care Medicine 174, no. 4 (2006): 400–407.

[228]

K.-J. Bai, A. P. Spicer, M. M. Mascarenhas, et al., “The Role of Hyaluronan Synthase 3 in Ventilator-Induced Lung Injury,” American Journal of Respiratory and Critical Care Medicine 172, no. 1 (2005): 92–98.

[229]

O. U. Gurkan, C. He, R. Zielinski, et al., “Interleukin-6 Mediates Pulmonary Vascular Permeability in a Two-Hit Model of Ventilator-Associated Lung Injury,” Experimental Lung Research 37, no. 10 (2011): 575–584.

[230]

J. A. Frank, J. F. Pittet, H. Lee, M. Godzich, and M. A. Matthay, “High Tidal Volume Ventilation Induces NOS2 and Impairs CAMP- Dependent Air Space Fluid Clearance,” American Journal of Physiology-Lung Cellular and Molecular Physiology 284, no. 5 (2003): L791–L798.

[231]

X. Peng, S. S. Raja, S. Fan, et al., “Inducible Nitric Oxide Synthase Contributes to Ventilator-Induced Lung Injury,” American Journal of Respiratory and Critical Care Medicine 172, no. 4 (2005): 470–479.

[232]

L. Ye, Q. Zeng, M. Ling, et al., “Inhibition of IP3R/Ca2+ Dysregulation Protects Mice From Ventilator-Induced Lung Injury via Endoplasmic Reticulum and Mitochondrial Pathways,” Frontiers in Immunology 12 (2021): 729094.

[233]

J.-S. Jiang, H.-C. Chou, L.-F. Wang, Y.-D. Lang, and C.-M. Chen, “Effects of Activated Protein C on Ventilator-Induced Lung Injury in Rats,” Respiration 80, no. 3 (2010): 246–253.

[234]

K. He, S. Han, L. An, and J. Zhang, “Inhibition of MicroRNA-214 Alleviates Lung Injury and Inflammation via Increasing FGFR1 Expression in Ventilator-Induced Lung Injury,” Lung 199, no. 1 (2021): 63–72.

[235]

S. Bertok, M. R. Wilson, P. J. Morley, R. Wildt, A. I. Bayliffe, and M. Takata, “Selective Inhibition of Intra-Alveolar P55 TNF Receptor Attenuates Ventilator-Induced Lung Injury,” Thorax 67, no. 3 (2011): 244–251.

[236]

H.-H. Li, Q. Li, P. Liu, et al., “WNT1-Inducible Signaling Pathway Protein 1 Contributes to Ventilator-Induced Lung Injury,” American Journal of Respiratory Cell and Molecular Biology 47, no. 4 (2012): 528–535.

[237]

R. Krishnan, J.-A. Park, C. Y. Seow, P. V.-S. Lee, and A. G. Stewart, “Cellular Biomechanics in Drug Screening and Evaluation: Mechanopharmacology,” Trends in Pharmacological Sciences 37, no. 2 (2016): 87–100.

[238]

A. Stewart, D. Denoyer, X. Gao, and Y.-C. Toh, “The FDA Modernisation Act 2.0: Bringing Non-Animal Technologies to the Regulatory Table,” Drug Discovery Today 28, no. 1 (2023): 103496.

[239]

B. C. Gabela-Zuniga, V. C. Shukla, C. Bobba, et al., “A Micro-Scale Humanized Ventilator-On-a-Chip to Examine the Injurious Effects of Mechanical Ventilation,” Lab on a Chip 24 (2024): 4390–4402.

[240]

A. G. Stewart, A. Gunatilaka, and B. Gao, “Should Culture Media for Microphysiological Systems Be Nutritionally Physiological?,” Nature Reviews Bioengineering 3, no. 5 (2025): 357–358.

[241]

A. McKechnie, H. A. Iliff, R. Black, et al., “Airway Management in Patients Living With Obesity: Best Practice Recommendations From the Society for Obesity and Bariatric Anaesthesia,” Anaesthesia 80, no. 9 (2025): 1103–1114.

[242]

T. J. Nolan, I. Dwyer, and P. Geoghegan, “The Use of Mechanical Ventilation in Interstitial Lung Disease,” Breathe 21, no. 2 (2025): 240172.

[243]

M. Felten, S. Ferencik, L.-G. T. Alves, et al., “Ventilator-Induced Lung Injury Is Modulated by the Circadian Clock,” American Journal of Respiratory and Critical Care Medicine 207, no. 11 (2022): 1464–1474.

[244]

S. Wiegert, F. Greco, P. Baumann, et al., “Impact of High Tidal Volume Ventilation on Surfactant Metabolism and Lung Injury in Infant Rats,” American Journal of Physiology-Lung Cellular and Molecular Physiology 319, no. 3 (2020): L562–L575.

[245]

Y. Kim, M. S. Ki, M. H. Shin, et al., “Thrombospondin-1 Modulation by Bifidobacterium Spp. Mitigates Lung Damage in an Acute Lung Injury Mouse Model,” Microbiological Research 297 (2025): 128173.

[246]

X. Yu, Y. Song, T. Dong, et al., “Citrullination of NF-ΚB P65 by PAD2 as a Novel Therapeutic Target for Modulating Macrophage Polarization in Acute Lung Injury,” Advanced Science 12, no. 18 (2025): e2413253.

[247]

M. Ruiz-Botella, S. Manrique, J. Gomez, and M. Bodí, “Advancing ICU Patient Care With a Real-Time Predictive Model for Mechanical Power to Mitigate VILI,” International Journal of Medical Informatics 189 (2024): 105511.

[248]

G. Emeriaud, Y. M. López-Fernández, N. P. Iyer, et al., “Executive Summary of the Second International Guidelines for the Diagnosis and Management of Pediatric Acute Respiratory Distress Syndrome (PALICC-2),” Pediatric Critical Care Medicine 24, no. 2 (2023): 143.

[249]

A. Medina, P. V. Guerra, J. R. V. Ortiz, and V. M. I. Alapont, “Rheological Theory Applied to Mechanical Ventilation in Acute Respiratory Distress Syndrome: A New Paradigm for Understanding and Preventing Ventilator-Induced Lung Injury,” Journal of Clinical Medicine 14, no. 18 (2025): 6544.

[250]

F. Rubulotta, L. B. Torra, K. D. Naidoo, et al., “Mechanical Ventilation, Past, Present, and Future,” Anesthesia and Analgesia 138, no. 2 (2024): 308–325.

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