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TGF‐β1‐induced connexin43 promotes scar formation via the Erk/MMP‐1/collagen III pathway
Author(s) -
Li Xiaoyan,
Guo Lijia,
Yang Xiaohui,
Wang Jingyi,
Hou Yanan,
Zhu Siying,
Du Juan,
Feng Jie,
Xie Yongmei,
Zhuang Li,
He Xin,
Liu Yi
Publication year - 2020
Publication title -
journal of oral rehabilitation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.991
H-Index - 93
eISSN - 1365-2842
pISSN - 0305-182X
DOI - 10.1111/joor.12829
Subject(s) - wound healing , mapk/erk pathway , matrix metalloproteinase , phosphorylation , chemistry , blot , microbiology and biotechnology , immunohistochemistry , immunofluorescence , pathology , medicine , biology , immunology , biochemistry , antibody , gene
Wound healing can be divided into different phases, and timely initiation and cessation of these stages is key to successful wound healing; otherwise, scar tissue forms in the wounded area. Connexins (Cxs) were confirmed to influence scar formation, and Cx43, an indispensable member of the Cx family, was shown to be involved in this process. Our study investigated the regulatory role of Cx43 in scar formation and the possible cell signalling pathways. We established oral mucosa and skin wound healing models in C57BL/6J mice. RT‐PCR, western blotting, immunohistochemistry and immunofluorescence were used to examine the expression of ECM components and key proteins in cell signalling pathways (TGF‐β1, Smad2/3, Cx43, Erk1/2 MMP‐1 and collagen III). After injury, buccal mucosa wounds healed with no scar, whereas skin wounds healed with an evident scar. Nevertheless, TGF‐β1 expression gradually increased by the 5th day after injury; Cx43 expression showed a similar response, with a progressive increase in the skin and a peak on day 14. In contrast, TGF‐β1 and Cx43 expression in the oral mucosa remained low. The high level of TGF‐β1 increased p‐Smad2/3 levels and then induced Cx43, whereas increased expression of Cx43 antagonised the phosphorylation of Erk1/2, a protein downstream of Cx43, which affected MMP‐1 synthesis. MMP‐1 deficiency led to collagen III accumulation and facilitated scar formation. We demonstrated that TGF‐β1‐induced Cx43 promotes scar formation via the Erk/MMP‐1/collagen III pathway.