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Airway epithelial regeneration requires autophagy and glucose metabolism.


ABSTRACT: Efficient repair of injured epithelium by airway progenitor cells could prevent acute inflammation from progressing into chronic phase in lung. Here, we used small molecules, genetic loss-of-function, organoid cultures, and in vivo lung-injury models to show that autophagy is essential for maintaining the pool of airway stem-like vClub cells by promoting their proliferation during ovalbumin-induced acute inflammation. Mechanistically, impaired autophagy disrupted glucose uptake in vClub progenitor cells, and either reduced accessibility to glucose or partial inhibition of glycolysis promoted the proliferative capacity of vClub progenitor cells and their daughter Club cells. However, glucose deprivation or glycolysis blockade abrogated the proliferative capacity of airway vClub cells and Club cells but promoted ciliated and goblet cell differentiation. Deficiency of glucose transporter-1 suppressed the proliferative capacity of airway progenitor cells after ovalbumin challenge. These findings suggested that autophagy and glucose metabolism are essential for the maintenance of airway epithelium at steady state and during allergic inflammation.

SUBMITTER: Li K 

PROVIDER: S-EPMC6868131 | biostudies-literature | 2019 Nov

REPOSITORIES: biostudies-literature

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Airway epithelial regeneration requires autophagy and glucose metabolism.

Li Kuan K   Li Minmin M   Li Wenli W   Yu Hongzhi H   Sun Xin X   Zhang Qiuyang Q   Li Yu Y   Li Xue X   Li Yue Y   Abel E Dale ED   Wu Qi Q   Chen Huaiyong H  

Cell death & disease 20191120 12


Efficient repair of injured epithelium by airway progenitor cells could prevent acute inflammation from progressing into chronic phase in lung. Here, we used small molecules, genetic loss-of-function, organoid cultures, and in vivo lung-injury models to show that autophagy is essential for maintaining the pool of airway stem-like vClub cells by promoting their proliferation during ovalbumin-induced acute inflammation. Mechanistically, impaired autophagy disrupted glucose uptake in vClub progenit  ...[more]

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