Effect of macrophage-to-myofibroblast transition on silicosis

Fei Geng , Jingrou Xu , Xichen Ren , Ying Zhao , Yuhao Cai , Yaqian Li , Fuyu Jin , Tian Li , Xuemin Gao , Wenchen Cai , Hong Xu , Zhongqiu Wei , Na Mao , Ying Sun , Fang Yang

Animal Models and Experimental Medicine ›› 2025, Vol. 8 ›› Issue (2) : 363 -371.

PDF (8049KB)
Animal Models and Experimental Medicine ›› 2025, Vol. 8 ›› Issue (2) : 363 -371. DOI: 10.1002/ame2.12470
ORIGINAL ARTICLE

Effect of macrophage-to-myofibroblast transition on silicosis

Author information +
History +
PDF (8049KB)

Abstract

Background: The aim was to explore the effect of macrophage polarization and macrophage-to-myofibroblast transition (MMT) in silicosis.

Methods: Male Wistar rats were divided into a control group and a silicosis group developed using a HOPE MED 8050 dynamic automatic dusting system. Murine macrophage MH-S cells were randomly divided into a control group and an SiO2 group. The pathological changes in lung tissue were observed using hematoxylin and eosin (HE) and Van Gieson (VG) staining. The distribution and location of macrophage marker (F4/80), M1 macrophage marker (iNOS), M2 macrophage marker (CD206), and myofibroblast marker (α-smooth muscle actin [α-SMA]) were detected using immunohistochemical and immunofluorescent staining. The expression changes in iNOS, Arg, α-SMA, vimentin, and type I collagen (Col I) were measured using Western blot.

Results: The results of HE and VG staining showed obvious silicon nodule formation and the distribution of thick collagen fibers in the lung tissue of the silicosis group. Macrophage marker F4/80 increased gradually from 8 to 32weeks after exposure to silica. Immunohistochemical and immunofluorescent staining results revealed that there were more iNOS-positive cells and some CD206-positive cells in the lung tissue of the silicosis group at 8weeks. More CD206-positive cells were found in the silicon nodules of the lung tissues in the silicosis group at 32weeks. Western blot analysis showed that the expressions of Inducible nitric oxide synthase and Arg protein in the lung tissues of the silicosis group were upregulated compared with those of the control group. The results of immunofluorescence staining showed the co-expression of F4/80, α-SMA, and Col I, and CD206 and α-SMA were co-expressed in the lung tissue of the silicosis group. The extracted rat alveolar lavage fluid revealed F4/80+α-SMA+, CD206+α-SMA+, and F4/80+α-SMA+Col I+ cells using immunofluorescence staining. Similar results were also found in MH-S cells induced by SiO2.

Conclusions: The development of silicosis is accompanied by macrophage polarization and MMT.

Keywords

macrophage / macrophage-to-myofibroblast transition / silicosis

Cite this article

Download citation ▾
Fei Geng, Jingrou Xu, Xichen Ren, Ying Zhao, Yuhao Cai, Yaqian Li, Fuyu Jin, Tian Li, Xuemin Gao, Wenchen Cai, Hong Xu, Zhongqiu Wei, Na Mao, Ying Sun, Fang Yang. Effect of macrophage-to-myofibroblast transition on silicosis. Animal Models and Experimental Medicine, 2025, 8(2): 363-371 DOI:10.1002/ame2.12470

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Handra CM, Gurzu IL, Chirila M, Ghita I. Silicosis: new challenges from an old inflammatory and fibrotic disease. Front Biosci. 2023;28(5):96.

[2]

Ryan FH, Daniel CC. Silica-related diseases in the modern world. Allergy. 2020;75(11):2805-2817.

[3]

Li T, Yang XY, Xu H, Liu H. Early identification, accurate diagnosis, and treatment of silicosis. Can Respir J. 2022;2022:3769134.

[4]

Amit K, Martin P. Roles of macrophage polarization and macrophage-derived miRNAs in pulmonary fibrosis. Front Immunol. 2021;12:678457.

[5]

Yang HD, Cheng H, Dai RR, Shang L, Zhang X, Wen H. Macrophage polarization in tissue fibrosis. PeerJ. 2023;11:e16092.

[6]

Wei J, Xu ZH, Yan X. The role of the macrophage-to-myofibroblast transition in renal fibrosis. Front Immunol. 2022;13:934377.

[7]

Vierhout M, Ayoub A, Naiel S, et al. Monocyte and macrophage derived myofibroblasts: is it fate? A review of the current evidence. Wound Repair Regen. 2021;29(4):548-562.

[8]

Meng XM, Thomas SKM, Lan HY. Macrophages in renal fibrosis. Adv Exp Med Biol. 2019;1165:285-303.

[9]

Paterson DJN, Wang S, Lan HY. Macrophages promote renal fibrosis through direct and indirect mechanisms. Kidney Int Suppl. 2014;4(1):34-38.

[10]

Wang S, Meng XM, Ng YY, et al. TGF-β/Smad3 signalling regulates the transition of bone marrowderived macrophages into myofibroblasts during tissue fibrosis. Oncotarget. 2016;7(8):8809-8822.

[11]

Meng XM, Wang S, Huang XR, et al. Inflammatory macrophages can transdifferentiate into myofibroblasts during renal fibrosis. Cell Death Dis. 2016;7(12):e2495.

[12]

Li YQ, Jin FY, Li T, et al. Minute cellular nodules as early lesions in rats with silica exposure via inhalation. Vet Sci. 2022;9(6):1-10.

[13]

Geng F, Zhao L, Cai YH, et al. Quercetin alleviates pulmonary fibrosis in Silicotic mice by inhibiting macrophage transition and TGF-β-Smad2/3 pathway. Curr Issues Mol Biol. 2023;45(4):3087-3101.

[14]

Cheng PY, Li SY, Chen HY. Macrophages in lung injury, repair, and fibrosis. Cells. 2021;10(2):1-10.

[15]

Lee JW, Chun WJ, Lee HJ, et al. The role of macrophages in the development of acute and chronic inflammatory lung diseases. Cells. 2021;10(4):1-9.

[16]

Shweta A, Kapil D, Beamon A, et al. Macrophages: their role, activation and polarization in pulmonary diseases. Immunobiology. 2018;223(4–5):383-396.

[17]

Elza E, Emma R, Tim W. Origin and ontogeny of lung macrophages: from mice to humans. Immunology. 2020;160(2):126-138.

[18]

Deng LS, Jian ZJ, Xu T, et al. Macrophage polarization: an important candidate regulator for lung diseases. Molecules (Basel, Switzerland). 2023;28(5):1-10.

[19]

Liu G, Ashleigh MP, Tamera C, et al. Therapeutic targets in lung tissue remodelling and fibrosis. Pharmacol Ther. 2021;225:107839.

[20]

Shoichiro S, Masahiro K, Noriko OS, et al. Angiopoietin-like 4 is a critical regulator of fibroblasts during pulmonary fibrosis development. Am J Respir Cell Mol Biol. 2023;69(3):328-339.

[21]

Ren ZN, Pan XH, Li JH, et al. G protein coupled receptor 41 regulates fibroblast activation in pulmonary fibrosis via Gαi/o and downstream Smad2/3 and ERK1/2 phosphorylation. Pharmacol Res. 2023;191:106754.

[22]

Li SM, Li YQ, Xu H, et al. ACE2 attenuates epithelial-mesenchymal transition in MLE-12 cells induced by silica. Drug Des Devel Ther. 2020;14:1547-1559.

[23]

Liu SP, Jin RT, Zheng GG, et al. Ac-SDKP promotes KIF3A-mediated β-catenin suppression through a ciliary mechanism to constrain silica-induced epithelial-myofibroblast transition. Biomed Pharmacother. 2023;166:115411.

[24]

Guo QT, Li P, Chen ML, et al. Exosomes from human umbilical cord stem cells suppress macrophage-to-myofibroblast transition, alleviating renal fibrosis. Inflammation. 2024;2024:1-10.

[25]

Yu WQ, Song JF, Chen SQ, et al. Myofibroblast-derived exosomes enhance macrophages to myofibroblasts transition and kidney fibrosis. Ren Fail. 2024;46(1):2334406.

[26]

Luo LH, Wang SJ, Hu YL, et al. Precisely regulating M2 subtype macrophages for renal fibrosis resolution. ACS Nano. 2023;17(22):22508-22526.

[27]

Gao Y, Liu BQ, Guo XQ, et al. Interferon regulatory factor 4 deletion protects against kidney inflammation and fibrosis in deoxycorticosterone acetate/salt hypertension. J Hypertens. 2023;41(5):794-810.

[28]

Yang F, Chang Y, Zhang CJ, et al. UUO induces lung fibrosis with macrophage-myofibroblast transition in rats. Int Immunopharmacol. 2021;93:107396.

[29]

Yi CJ, Liu J, Deng W, et al. Macrophage elastase (MMP12) critically contributes to the development of subretinal fibrosis. J Neuroinflammation. 2022;19(1):78.

[30]

Karis L, Maria LS, Tang M, et al. Macrophage to myofibroblast transition contributes to subretinal fibrosis secondary to neovascular age-related macular degeneration. J Neuroinflammation. 2020;17(1):355.

[31]

Zhuang T, Chen H, Wu RX, et al. ALKBH5-mediated m6A modification of IL-11 drives macrophage-to-myofibroblast transition and pathological cardiac fibrosis in mice. Nat Commun. 2024;15(1):1995.

[32]

Shen SC, Zhang M, Wang XH, et al. Single-cell RNA sequencing reveals S100a9hi macrophages promote the transition from acute inflammation to fibrotic remodeling after myocardial ischemia–reperfusion. Theranostics. 2024;14(3):1241-1259.

[33]

Han YT, Xian YQ, Gao XM, et al. Eplerenone inhibits the macrophage-to-myofibroblast transition in rats with UUO-induced type 4 cardiorenal syndrome through the MR/CTGF pathway. Int Immunopharmacol. 2022;113:109396.

[34]

Qi BJ, Li YQ, Peng Z, et al. Macrophage-myofibroblast transition as a potential origin for skeletal muscle fibrosis after injury via complement system activation. J Inflamm Res. 2024;17:1083-1094.

[35]

Xia SH, Huang YJ, Zhang Y, et al. Role of macrophage-to-myofibroblast transition in chronic liver injury and liver fibrosis. Eur J Med Res. 2023;28(1):502.

[36]

Shan Y, Yu MS, Dai HB, et al. The role of macrophage-derived exosomes in reversing peritoneal fibrosis: insights from Astragaloside IV. Phytomedicine. 2024;129:155683.

[37]

Liu HJ, Guan QZ, Zhao P, Li J. TGF-β-induced CCR8 promoted macrophage transdifferentiation into myofibroblast-like cells. Exp Lung Res. 2022;4:1-14.

RIGHTS & PERMISSIONS

2024 The Author(s). Animal Models and Experimental Medicine published by John Wiley & Sons Australia, Ltd on behalf of The Chinese Association for Laboratory Animal Sciences.

AI Summary AI Mindmap
PDF (8049KB)

358

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/