Department of Pharmacology and the Cancer Institute of New Jersey, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, Piscataway, NJ 08854, USA.
Pharmacol Res. 2012 Dec;66(6):505-12. doi: 10.1016/j.phrs.2012.09.004. Epub 2012 Sep 24.
Obesity, which predisposes individuals to type II diabetes and cardiovascular diseases, results from accumulation of white adipose tissue (WAT). WAT comprises mainly white adipocytes that have a unique cellular structure in which almost the entire intracellular space is occupied by one single lipid droplet. The cytoplasm envelopes this lipid droplet and occupies negligible space. Differentiation of WAT, or adipogenesis, requires dramatic cytoplasmic reorganization, including a dynamic change in mitochondrial mass. Autophagy is a major cytoplasmic degradation pathway and a primary pathway for mitochondrial degradation. Recent studies indicate that autophagy is implicated in adipogenesis. In this review, we summarize our current knowledge on autophagy in adipose tissue biology, with the emphasis on its role in mitochondrial degradation. Adipose tissue is a central component for whole-body energy homeostasis regulation. Advancement in this research area may provide novel venues for the intervention of obesity and obesity related diseases.
肥胖会导致个体易患 II 型糖尿病和心血管疾病,它是由白色脂肪组织(WAT)的积累引起的。WAT 主要由白色脂肪细胞组成,这些细胞具有独特的细胞结构,其中几乎整个细胞内空间都被一个单独的脂滴占据。细胞质包围着这个脂滴,几乎没有空间。WAT 的分化,或脂肪生成,需要细胞质的剧烈重组,包括线粒体质量的动态变化。自噬是一种主要的细胞质降解途径,也是线粒体降解的主要途径。最近的研究表明,自噬参与了脂肪生成。在这篇综述中,我们总结了我们目前对脂肪组织生物学中自噬的认识,重点介绍了它在线粒体降解中的作用。脂肪组织是全身能量稳态调节的核心组成部分。这一研究领域的进展可能为肥胖和肥胖相关疾病的干预提供新的途径。