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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Bibliografiset tiedot
Julkaisussa:Cell Death Dis
Päätekijät: Wang, Jie, Xu, Lizhi, Xiang, Zou, Ren, Yan, Zheng, Xiufen, Zhao, Qingya, Zhou, Qunzhi, Zhou, Yuefen, Xu, Lin, Wang, Yaping
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Nature Publishing Group UK 2020
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7031231/
https://ncbi.nlm.nih.gov/pubmed/32075954
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41419-020-2329-z
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