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The Liver as an Endocrine Organ-Linking NAFLD and Insulin Resistance

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ENDOCRINE REVIEWS
卷 40, 期 5, 页码 1367-1393

出版社

ENDOCRINE SOC
DOI: 10.1210/er.2019-00034

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资金

  1. National Health and Medical Research Council of Australia Senior Research Fellowship [APP1077703]
  2. Natural Sciences and Engineering Research Council of Canada Postdoctoral Fellowship
  3. Melbourne Research Scholarship (University of Melbourne)
  4. National Health and Medical Research Council of Australia Career Development Fellowship [APP1143224]
  5. National Health and Medical Research Council of Australia [APP1162511, APP1156508]

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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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