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Epithelial cell senescence induces pulmonary fibrosis through Nanog-mediated fibroblast activation.


ABSTRACT: Idiopathic pulmonary fibrosis (IPF) is a chronic and progressive lung disease tightly correlated with aging. The pathological features of IPF include epithelial cell senescence and abundant foci of highly activated pulmonary fibroblasts. However, the underlying mechanism between epithelial cell senescence and pulmonary fibroblast activation remain to be elucidated. In our study, we demonstrated that Nanog, as a pluripotency gene, played an essential role in the activation of pulmonary fibroblasts. In the progression of IPF, senescent epithelial cells could contribute to the activation of pulmonary fibroblasts via increasing the expression of senescence-associated secretory phenotype (SASP). In addition, we found activated pulmonary fibroblasts exhibited aberrant activation of Wnt/?-catenin signalling and elevated expression of Nanog. Further study revealed that the activation of Wnt/?-catenin signalling was responsible for senescent epithelial cell-induced Nanog phenotype in pulmonary fibroblasts. ?-catenin was observed to bind to the promoter of Nanog during the activation of pulmonary fibroblasts. Targeted inhibition of epithelial cell senescence or Nanog could effectively suppress the activation of pulmonary fibroblasts and impair the development of pulmonary fibrosis, indicating a potential for the exploration of novel anti-fibrotic strategies.

SUBMITTER: Chen X 

PROVIDER: S-EPMC6977687 | biostudies-literature | 2019 Dec

REPOSITORIES: biostudies-literature

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Epithelial cell senescence induces pulmonary fibrosis through Nanog-mediated fibroblast activation.

Chen Xiang X   Xu Hongyang H   Hou Jiwei J   Wang Hui H   Zheng Yi Y   Li Hui H   Cai Hourong H   Han Xiaodong X   Dai Jinghong J  

Aging 20191231 1


Idiopathic pulmonary fibrosis (IPF) is a chronic and progressive lung disease tightly correlated with aging. The pathological features of IPF include epithelial cell senescence and abundant foci of highly activated pulmonary fibroblasts. However, the underlying mechanism between epithelial cell senescence and pulmonary fibroblast activation remain to be elucidated. In our study, we demonstrated that Nanog, as a pluripotency gene, played an essential role in the activation of pulmonary fibroblast  ...[more]

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