胰岛素抵抗
生物
内科学
非酒精性脂肪肝
内分泌学
脂质代谢
医学
胰岛素
脂肪组织
脂肪肝
肝病
内分泌系统
微泡
生物信息学
激素
小RNA
疾病
生物化学
基因
作者
Matthew J. Watt,Paula M. Miotto,William De Nardo,Magdalene K. Montgomery
出处
期刊:Endocrine Reviews
[Oxford University Press]
日期:2019-04-25
卷期号:40 (5): 1367-1393
被引量:467
标识
DOI:10.1210/er.2019-00034
摘要
The liver is a dynamic organ that plays critical roles in many physiological processes, including the regulation of systemic glucose and lipid metabolism. Dysfunctional hepatic lipid metabolism is a cause of nonalcoholic fatty liver disease (NAFLD), the most common chronic liver disorder worldwide, and is closely associated with insulin resistance and type 2 diabetes. Through the use of advanced mass spectrometry "omics" approaches and detailed experimentation in cells, mice, and humans, we now understand that the liver secretes a wide array of proteins, metabolites, and noncoding RNAs (miRNAs) and that many of these secreted factors exert powerful effects on metabolic processes both in the liver and in peripheral tissues. In this review, we summarize the rapidly evolving field of "hepatokine" biology with a particular focus on delineating previously unappreciated communication between the liver and other tissues in the body. We describe the NAFLD-induced changes in secretion of liver proteins, lipids, other metabolites, and miRNAs, and how these molecules alter metabolism in liver, muscle, adipose tissue, and pancreas to induce insulin resistance. We also synthesize the limited information that indicates that extracellular vesicles, and in particular exosomes, may be an important mechanism for intertissue communication in normal physiology and in promoting metabolic dysregulation in NAFLD.
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