Microcystin-LR ameliorates pulmonary fibrosis via modulating CD206(+) M2-like macrophage polarization

Idiopathic pulmonary fibrosis (IPF) is a group of chronic interstitial pulmonary diseases characterized by myofibroblast proliferation and extracellular matrix deposition with limited treatment options. Based on our previous observation, we hypothesized microcystin-leucine arginine (LR), an environm...

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Detalles Bibliográficos
Autores principales: Wang, Jie, Xu, Lizhi, Xiang, Zou, Ren, Yan, Zheng, Xiufen, Zhao, Qingya, Zhou, Qunzhi, Zhou, Yuefen, Xu, Lin, Wang, Yaping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7031231/
https://www.ncbi.nlm.nih.gov/pubmed/32075954
http://dx.doi.org/10.1038/s41419-020-2329-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7031231/
https://www.ncbi.nlm.nih.gov/pubmed/32075954
http://dx.doi.org/10.1038/s41419-020-2329-z

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