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Inhibition of miR-155-5p Exerts Anti-Fibrotic Effects in Silicotic Rats by Regulating Meprin α

30 Pages Posted: 7 Aug 2019

See all articles by Yingying Chen

Yingying Chen

North China University of Science and Technology - Medical Research Center

Dingjie Xu

North China University of Science and Technology

Yao Jingxin

North China University of Science and Technology - Medical Research Center

Zhongqiu Wei

North China University of Science and Technology

Shifeng Li

North China University of Science and Technology - Medical Research Center

Xuemin Gao

North China University of Science and Technology - Medical Research Center

Wenchen Cai

North China University of Science and Technology - School of Public Health

Na Mao

North China University of Science and Technology - School of Public Health

Fuyu Jin

North China University of Science and Technology - Medical Research Center

Yaqian Li

North China University of Science and Technology - Medical Research Center

Fang Yang

North China University of Science and Technology - Medical Research Center

Hong Xu

North China University of Science and Technology - Medical Research Center

More...

Abstract

Silicosis is a fatal profession-related disease linked to long term inhalation of silica. The present study aimed to determine whether meprin α, a master regulator of anti-fibrotic peptide N-acetyl-serylaspartyl-lysyl-proline (Ac-SDKP), is diminished by miR-155-5p in silicosis and control lung macrophages and fibroblasts upon activation. RAW 264.7 macrophages, primary lung fibroblasts, and mouse embryonic fibroblasts were used to evaluate the expression and function of meprin α and miR-155-5p. In vitro meprin α manipulation was performed by recombinant mouse meprin α protein, actinonin (its inhibitor), and small interfering RNA knockdown. Macrophage and fibroblast activation was assessed by western blotting, real-time PCR, matrix deposition, immunohistochemistry, and immunofluorescence staining. The roles of meprin α and miR-155-5p were also investigated in mice exposed to silica. We found that the meprin α level was stably repressed in silicotic rats.In vitro, silica decreased meprin α, and exogenous meprin α reduced activation of macrophages and fibroblasts induced by profibrotic factors. MiR-155-5p negatively regulated Mep1a by binding to the 3′ untranslated region. Treatment with anti-miR-155-5p elevated meprin α, ameliorated macrophage and fibroblast activation, and attenuated lung fibrosis in mice induced by silica. The sustained repression of meprin α and beneficial effects of its rescue by inhibition of miR-155-5p during silicosis indicate that miR-155-5p/meprin α are major regulators of silicosis.

Funding Statement: This work was supported by the National Natural Science Foundation of China (No. 81472953), the Natural Science Foundation of Hebei Province (No. H20162091705), Science and Technology Research Project of Hebei Province universities (No. ZD2019077), and the Preeminence Youth Foundation of North China University of Science and Technology (JP201513).

Declaration of Interests: The authors declare they have no competing interests.

Ethics Approval Statement: All experimental and surgical procedures were approved (2013-038 and 2017-025) by the Ethics Committee for Animal Experimentation of North China University of Science and Technology, which complies with the US National Institutes of Health Guide for the Care and Use of Laboratory Animals.

Suggested Citation

Chen, Yingying and Xu, Dingjie and Jingxin, Yao and Wei, Zhongqiu and Li, Shifeng and Gao, Xuemin and Cai, Wenchen and Mao, Na and Jin, Fuyu and Li, Yaqian and Yang, Fang and Xu, Hong, Inhibition of miR-155-5p Exerts Anti-Fibrotic Effects in Silicotic Rats by Regulating Meprin α (August 5, 2019). Available at SSRN: https://ssrn.com/abstract=3432555 or http://dx.doi.org/10.2139/ssrn.3432555

Yingying Chen

North China University of Science and Technology - Medical Research Center

Hebei
China

Dingjie Xu

North China University of Science and Technology

No. 5, Jinyuanzhuang Road, Shijingshan District
Beijing
China

Yao Jingxin

North China University of Science and Technology - Medical Research Center

Hebei
China

Zhongqiu Wei

North China University of Science and Technology

No. 5, Jinyuanzhuang Road, Shijingshan District
Beijing
China

Shifeng Li

North China University of Science and Technology - Medical Research Center

Hebei
China

Xuemin Gao

North China University of Science and Technology - Medical Research Center

Hebei
China

Wenchen Cai

North China University of Science and Technology - School of Public Health

China

Na Mao

North China University of Science and Technology - School of Public Health

China

Fuyu Jin

North China University of Science and Technology - Medical Research Center

Hebei
China

Yaqian Li

North China University of Science and Technology - Medical Research Center

Hebei
China

Fang Yang

North China University of Science and Technology - Medical Research Center

Hebei
China

Hong Xu (Contact Author)

North China University of Science and Technology - Medical Research Center ( email )

Hebei
China

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