Effect of macrophage-to-myofibroblast transition on silicosis
Fei Geng1
Jingrou Xu2
Xichen Ren2
Ying Zhao2
Yuhao Cai2
Yaqian Li2
Fuyu Jin2
Tian Li2
Xuemin Gao2
Wenchen Cai2
Hong Xu2
Zhongqiu Wei3
Na Mao2
Ying Sun3
Fang Yang2
1.Hebei Key Laboratory for Organ Fibrosis Research,School of Public Health,North China University of Science and Technology,Tangshan,China;Department of Pathology,Hebei Key Laboratory for Chronic Diseases,School of Basic Medical Sciences,North China University of Science and Technology,Tangshan,China2.Hebei Key Laboratory for Organ Fibrosis Research,School of Public Health,North China University of Science and Technology,Tangshan,China3.Department of Pathology,Hebei Key Laboratory for Chronic Diseases,School of Basic Medical Sciences,North China University of Science and Technology,Tangshan,China
摘要: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 mac-rophage MH-S cells were randomly divided into a control group and an SiO 2 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 immu-nohistochemical 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 32 weeks 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 8 weeks.More CD206-positive cells were found in the silicon nodules of the lung tissues in the silicosis group at 32 weeks.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 con-trol 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 SiO 2. Conclusions:The development of silicosis is accompanied by macrophage polarization and MMT.
机标关键词:effectmacrophagemyofibroblastsilicosistransition
论文发表日期:2025-02-28
在线出版日期:2025-08-15(本平台首次上网日期,不代表文献的发表时间)
页数:9( 363-371 )
英文信息展开
动物模型与实验医学(英文)

动物模型与实验医学(英文)

CSCD
ISSN:2096-5451
年,卷(期):2025,8(2)
所属栏目:Original Article