自噬体
自噬
脂肪生成
溶酶体
细胞生物学
脂肪细胞
脂滴
化学
生物
脂质代谢
生物化学
脂肪组织
酶
细胞凋亡
作者
Leslie A. Rowland,Adı́lson Guilherme,Felipe Henriques,Chloe DiMarzio,Sean Munroe,Nicole Wetoska,Mark Kelly,Keith Reddig,Gregory Hendricks,Meixia Pan,Xianlin Han,Olga Ilkayeva,Christopher B. Newgard,Michael Czech
标识
DOI:10.1038/s41467-023-37016-8
摘要
Abstract Adipocytes robustly synthesize fatty acids (FA) from carbohydrate through the de novo lipogenesis (DNL) pathway, yet surprisingly DNL contributes little to their abundant triglyceride stored in lipid droplets. This conundrum raises the hypothesis that adipocyte DNL instead enables membrane expansions to occur in processes like autophagy, which requires an abundant supply of phospholipids. We report here that adipocyte Fasn deficiency in vitro and in vivo markedly impairs autophagy, evident by autophagosome accumulation and severely compromised degradation of the autophagic substrate p62. Our data indicate the impairment occurs at the level of autophagosome-lysosome fusion, and indeed, loss of Fasn decreases certain membrane phosphoinositides necessary for autophagosome and lysosome maturation and fusion. Autophagy dependence on FA produced by Fasn is not fully alleviated by exogenous FA in cultured adipocytes, and interestingly, imaging studies reveal that Fasn colocalizes with nascent autophagosomes. Together, our studies identify DNL as a critical source of FAs to fuel autophagosome and lysosome maturation and fusion in adipocytes.
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