脂解
脂肪组织
胞浆
脂肪甘油三酯脂肪酶
内分泌学
内科学
背景(考古学)
脂质代谢
生物
脂肪生成
代谢途径
溶酶体
脂滴
化学
线粒体
调节器
白色脂肪组织
甘油三酯
细胞生物学
代谢综合征
β氧化
新陈代谢
生物化学
脂肪酸代谢
脂肪酸
脂滴包被蛋白
三磷酸腺苷
作者
Yeh Yu-Sheng,Jun Huang,Ziyang Liu,Carlos Cosme,Xiangyu Zhang,Babak Razani
标识
DOI:10.1161/atvbaha.125.323273
摘要
Adipose tissue lipid metabolism is a critical regulator of systemic energy balance, but its impact on cardiometabolic health is paradoxical. This review dissects the 2 primary lipolytic systems in adipocytes: the canonical cytosolic pathway driven by ATGL/PNPLA2 (adipose triglyceride lipase) and the lysosomal pathway governed by LAL/LIPA (lysosomal acid lipase). We present emerging evidence that these pathways exert opposing effects in the context of obesity. While excessive fatty acid efflux from dysregulated cytosolic lipolysis is a known driver of adiposopathic dyslipidemia, adipose inflammation, and direct cardiac lipotoxicity, which collectively impair cardiometabolic health, the activity of the lysosomal pathway is emerging as a protective counterbalance. Genetic and pharmacological studies demonstrate that inhibiting cytosolic ATGL is beneficial for metabolic health, whereas enhancing LAL-mediated lipolysis mitigates obesity-related dysfunction. This functional antagonism between cytosolic and lysosomal lipolysis presents a new paradigm in lipid metabolism, suggesting that therapeutic strategies must be pathway-specific. We conclude that selectively inhibiting pathogenic cytosolic lipid release while promoting beneficial lysosomal lipid processing offers a nuanced approach to treating metabolic disease.
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