Airway Basal Stem Cells Inflammatory Alterations in COVID-19 and Mitigation by Mesenchymal Stem Cells

Sheng Du , Jing Jin , Chunli Tang , Zhuquan Su , Lulin Wang , Xinyuan Chen , Mengni Zhang , Yiping Zhu , Jiaojiao Wang , Chunrong Ju , Xinyu Song , Shiyue Li

Cell Proliferation ›› 2025, Vol. 58 ›› Issue (6) : e13812

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Cell Proliferation ›› 2025, Vol. 58 ›› Issue (6) : e13812 DOI: 10.1111/cpr.13812
ORIGINAL ARTICLE

Airway Basal Stem Cells Inflammatory Alterations in COVID-19 and Mitigation by Mesenchymal Stem Cells

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Abstract

SARS-CoV-2 infection and the resultant COVID-19 pneumonia cause significant damage to the airway and lung epithelium. This damage manifests as mucus hypersecretion, pulmonary inflammation and fibrosis, which often lead to long-term complications collectively referred to as long COVID or post-acute sequelae of COVID-19 (PASC). The airway epithelium, as the first line of defence against respiratory pathogens, depends on airway basal stem cells (BSCs) for regeneration. Alterations in BSCs are associated with impaired epithelial repair and may contribute to the respiratory complications observed in PASC. Given the critical role of BSCs in maintaining epithelial integrity, understanding their alterations in COVID-19 is essential for developing effective therapeutic strategies. This study investigates the intrinsic properties of BSCs derived from COVID-19 patients and evaluates the modulatory effects of mesenchymal stem cells (MSCs). Through a combination of functional assessments and transcriptomic profiling, we identified key phenotypic and molecular deviations in COVID-19 patient-derived BSCs, including goblet cell hyperplasia, inflammation and fibrosis, which may underlie their contribution to PASC. Notably, MSC co-culture significantly mitigated these adverse effects, potentially through modulation of the interferon signalling pathway. This is the first study to isolate BSCs from COVID-19 patients in the Chinese population and establish a COVID-19 BSC-based xenograft model. Our findings reveal critical insights into the role of BSCs in epithelial repair and their inflammatory alterations in COVID-19 pathology, with potential relevance to PASC and virus-induced respiratory sequelae. Additionally, our study highlights MSC-based therapies as a promising strategy to address respiratory sequelae and persistent symptoms.

Keywords

airway basal stem cells / COVID-19 / fibrosis / goblet cell hyperplasia / inflammation / mesenchymal stem cells / post-acute sequelae of COVID-19

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Sheng Du, Jing Jin, Chunli Tang, Zhuquan Su, Lulin Wang, Xinyuan Chen, Mengni Zhang, Yiping Zhu, Jiaojiao Wang, Chunrong Ju, Xinyu Song, Shiyue Li. Airway Basal Stem Cells Inflammatory Alterations in COVID-19 and Mitigation by Mesenchymal Stem Cells. Cell Proliferation, 2025, 58(6): e13812 DOI:10.1111/cpr.13812

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References

[1]

W. J. Guan, Z. Y. Ni, Y. Hu, et al., “Clinical Characteristics of Coronavirus Disease 2019 in China,” New England Journal of Medicine 382 (2020): 1708-1720.

[2]

C. B. Jackson, M. Farzan, B. Chen, and H. Choe, “Mechanisms of SARS-CoV-2 Entry Into Cells,” Nature Reviews. Molecular Cell Biology 23 (2022): 3-20.

[3]

A. V. Ballering, S. K. R. van Zon, H. T. C. Olde, and J. G. M. Rosmalen, “Persistence of Somatic Symptoms After COVID-19 in The Netherlands: An Observational Cohort Study,” Lancet 400 (2022): 452-461.

[4]

M. Parotto, M. Gyöngyösi, K. Howe, et al., “Post-Acute Sequelae of COVID-19: Understanding and Addressing the Burden of Multisystem Manifestations,” Lancet Respiratory Medicine 11 (2023): 739-754.

[5]

J. Baggen, M. Jacquemyn, L. Persoons, et al., “TMEM106B Is a Receptor Mediating ACE2-Independent SARS-CoV-2 Cell Entry,” Cell 186 (2023): 3427-3442.e3422.

[6]

B. F. Dickey, J. Chen, and R. S. Peebles, “Airway Mucus Dysfunction in COVID-19,” American Journal of Respiratory and Critical Care Medicine 206 (2022): 1304-1306.

[7]

T. Kato, T. Asakura, C. E. Edwards, et al., “Prevalence and Mechanisms of Mucus Accumulation in COVID-19 Lung Disease,” American Journal of Respiratory and Critical Care Medicine 206 (2022): 1336-1352.

[8]

D. Blanco-Melo, B. E. Nilsson-Payant, W. C. Liu, et al., “Imbalanced Host Response to SARS-CoV-2 Drives Development of COVID-19,” Cell 181 (2020): 1036-1045.e1039.

[9]

S. Khan, M. S. Shafiei, C. Longoria, J. W. Schoggins, R. C. Savani, and H. Zaki, “SARS-CoV-2 Spike Protein Induces Inflammation via TLR2-Dependent Activation of the NF-κB Pathway,” eLife 10 (2021): e68563.

[10]

T. M. Delorey, C. G. K. Ziegler, G. Heimberg, et al., “COVID-19 Tissue Atlases Reveal SARS-CoV-2 Pathology and Cellular Targets,” Nature 595 (2021): 107-113.

[11]

J. C. Melms, J. Biermann, H. Huang, et al., “A Molecular Single-Cell Lung Atlas of Lethal COVID-19,” Nature 595 (2021): 114-119.

[12]

M. Merad, C. A. Blish, F. Sallusto, and A. Iwasaki, “The Immunology and Immunopathology of COVID-19,” Science 375 (2022): 1122-1127.

[13]

D. Wendisch, O. Dietrich, T. Mari, et al., “SARS-CoV-2 Infection Triggers Profibrotic Macrophage Responses and Lung Fibrosis,” Cell 184 (2021): 6243-6261.e6227.

[14]

P. M. George, A. U. Wells, and R. G. Jenkins, “Pulmonary Fibrosis and COVID-19: The Potential Role for Antifibrotic Therapy,” Lancet Respiratory Medicine 8 (2020): 807-815.

[15]

J. A. Zepp and E. E. Morrisey, “Cellular Crosstalk in the Development and Regeneration of the Respiratory System,” Nature Reviews. Molecular Cell Biology 20 (2019): 551-566.

[16]

M. C. Basil, K. D. Alysandratos, D. N. Kotton, and E. E. Morrisey, “Lung Repair and Regeneration: Advanced Models and Insights Into Human Disease,” Cell Stem Cell 31 (2024): 439-454.

[17]

Y. Fang, H. Liu, H. Huang, et al., “Distinct Stem/Progenitor Cells Proliferate to Regenerate the Trachea, Intrapulmonary Airways and Alveoli in COVID-19 Patients,” Cell Research 30 (2020): 705-707.

[18]

S. Wang, W. Rao, A. Hoffman, et al., “Cloning a Profibrotic Stem Cell Variant in Idiopathic Pulmonary Fibrosis,” Science Translational Medicine 15 (2023): eabp9528.

[19]

W. Rao, S. Wang, M. Duleba, et al., “Regenerative Metaplastic Clones in COPD Lung Drive Inflammation and Fibrosis,” Cell 181 (2020): 848-864.e818.

[20]

X. Han, C. Cai, W. Deng, et al., “Landscape of Human Organoids: Ideal Model in Clinics and Research,” Innovation (Cambridge) 5 (2024): 100620, https://doi.org/10.1016/j.xinn.2024.100620.

[21]

L. Shi, L. Wang, R. Xu, et al., “Mesenchymal Stem Cell Therapy for Severe COVID-19,” Signal Transduction and Targeted Therapy 6 (2021): 339.

[22]

X. Chen, J. Huang, J. Wu, et al., “Human Mesenchymal Stem Cells,” Cell Proliferation 55 (2022): e13141, https://doi.org/10.1111/cpr.13141.

[23]

J. Hao, A. Ma, L. Wang, et al., “General Requirements for Stem Cells,” Cell Proliferation 53 (2020): e12926, https://doi.org/10.1111/cpr.12926.

[24]

T. Wu, E. Hu, S. Xu, et al., “clusterProfiler 4.0: A Universal Enrichment Tool for Interpreting Omics Data,” Innovation (Cambridge) 2 (2021): 100141, https://doi.org/10.1016/j.xinn.2021.100141.

[25]

Z. Zhang, L. Guo, L. Huang, et al., “Distinct Disease Severity Between Children and Older Adults With Coronavirus Disease 2019 (COVID-19): Impacts of ACE2 Expression, Distribution, and Lung Progenitor Cells,” Clinical Infectious Diseases 73 (2021): e4154-e4165, https://doi.org/10.1093/cid/ciaa1911.

[26]

K. Bankoti, W. Wang, G. M. Amonkar, et al., “Airway Basal Stem Cells in COVID-19 Exhibit a Proinflammatory Signature and Impaired Mucocililary Differentiation,” American Journal of Respiratory Cell and Molecular Biology 70 (2024): 26-38.

[27]

A. Purkayastha, C. Sen, G. Garcia, et al., “Direct Exposure to SARS-CoV-2 and Cigarette Smoke Increases Infection Severity and Alters the Stem Cell-Derived Airway Repair Response,” Cell Stem Cell 27 (2020): 869-875.e864.

[28]

S. Hao, K. Ning, C. A. Kuz, K. Vorhies, Z. Yan, and J. Qiu, “Long-Term Modeling of SARS-CoV-2 Infection of In Vitro Cultured Polarized Human Airway Epithelium,” MBio 11 (2020): 02852-20.

[29]

N. G. Ravindra, M. M. Alfajaro, V. Gasque, et al., “Single-Cell Longitudinal Analysis of SARS-CoV-2 Infection in Human Airway Epithelium Identifies Target Cells, Alterations in Gene Expression, and Cell State Changes,” PLoS Biology 19 (2021): e3001143.

[30]

S. Rustam, Y. Hu, S. B. Mahjour, et al., “A Unique Cellular Organization of Human Distal Airways and its Disarray in Chronic Obstructive Pulmonary Disease,” American Journal of Respiratory and Critical Care Medicine 207 (2023): 1171-1182.

[31]

K. van der Ploeg, A. S. Kirosingh, D. A. M. Mori, et al., “TNF-α (+) CD4 (+) T Cells Dominate the SARS-CoV-2 Specific T Cell Response in COVID-19 Outpatients and Are Associated With Durable Antibodies,” Cell Reports Medicine 3 (2022): 100640, https://doi.org/10.1016/j.xcrm.2022.100640.

[32]

G. Chen, D. Wu, W. Guo, et al., “Clinical and Immunological Features of Severe and Moderate Coronavirus Disease 2019,” Journal of Clinical Investigation 130 (2020): 2620-2629, https://doi.org/10.1172/jci137244.

[33]

F. Duan, L. Guo, L. Yang, et al., “Modeling COVID-19 With Human Pluripotent Stem Cell-Derived Cells Reveals Synergistic Effects of Anti-Inflammatory Macrophages With ACE2 Inhibition Against SARS-CoV-2,” Research Square (2020), https://doi.org/10.21203/rs.3.rs-62758/v1.

[34]

L. Shi, X. Yuan, W. Yao, et al., “Human Mesenchymal Stem Cells Treatment for Severe COVID-19: 1-Year Follow-Up Results of a Randomized, Double-Blind, Placebo-Controlled Trial,” eBioMedicine 75 (2022): 103789, https://doi.org/10.1016/j.ebiom.2021.103789.

[35]

N. Işıksaçan, G. Adaş, P. Kasapoğlu, et al., “The Effect of Mesenchymal Stem Cells Administration on DNA Repair Gene Expressions in Critically Ill COVID-19 Patients: Prospective Controlled Study,” Nucleosides, Nucleotides and Nucleic Acids 1-16 (2024): 1431-1446, https://doi.org/10.1080/15257770.2024.2327478.

[36]

M. W. Poon, L. Yan, D. Jiang, et al., “Inhibition of RAP1 Enhances Corneal Recovery Following Alkali Injury,” Investigative Ophthalmology and Visual Science 56 (2015): 711-721, https://doi.org/10.1167/iovs.14-15268.

[37]

C. Y. Ma, Y. Zhai, C. T. Li, et al., “Translating Mesenchymal Stem Cell and Their Exosome Research Into GMP Compliant Advanced Therapy Products: Promises, Problems and Prospects,” Medicinal Research Reviews 44 (2024): 919-938, https://doi.org/10.1002/med.22002.

[38]

T. T. Li, B. Zhang, H. Fang, et al., “Human Mesenchymal Stem Cell Therapy in Severe COVID-19 Patients: 2-Year Follow-Up Results of a Randomized, Double-Blind, Placebo-Controlled Trial,” eBioMedicine 92 (2023): 104600.

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2025 The Author(s). Cell Proliferation published by Beijing Institute for Stem Cell and Regenerative Medicine and John Wiley & Sons Ltd.

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