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Control of Adipocyte Differentiation in Different Fat Depots; Implications for Pathophysiology or Therapy
Adipocyte differentiation and its impact on restriction or expansion of particular adipose tissue depots have physiological and pathophysiological significance in view of the different functions of these depots. Brown or “beige” fat [brown adipose tissue (BAT)] expansion can enhance thermogenesis, l...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4311677/ https://www.ncbi.nlm.nih.gov/pubmed/25688231 http://dx.doi.org/10.3389/fendo.2015.00001 |
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author | Ma, Xiuquan Lee, Paul Chisholm, Donald J. James, David E. |
author_facet | Ma, Xiuquan Lee, Paul Chisholm, Donald J. James, David E. |
author_sort | Ma, Xiuquan |
collection | PubMed |
description | Adipocyte differentiation and its impact on restriction or expansion of particular adipose tissue depots have physiological and pathophysiological significance in view of the different functions of these depots. Brown or “beige” fat [brown adipose tissue (BAT)] expansion can enhance thermogenesis, lipid oxidation, insulin sensitivity, and glucose tolerance; conversely expanded visceral fat [visceral white adipose tissue (VAT)] is associated with insulin resistance, low grade inflammation, dyslipidemia, and cardiometabolic risk. The largest depot, subcutaneous white fat [subcutaneous white adipose tissue (SAT)], has important beneficial characteristics including storage of lipid “out of harms way” and secretion of adipokines, especially leptin and adiponectin, with positive metabolic effects including lipid oxidation, energy utilization, enhanced insulin action, and an anti-inflammatory role. The absence of these functions in lipodystrophies leads to major metabolic disturbances. An ability to expand white adipose tissue adipocyte differentiation would seem an important defense mechanism against the detrimental effects of energy excess and limit harmful accumulation of lipid in “ectopic” sites, such as liver and muscle. Adipocyte differentiation involves a transcriptional cascade with PPARγ being most important in SAT but less so in VAT, with increased angiogenesis also critical. The transcription factor, Islet1, is fairly specific to VAT and in vitro inhibits adipocyte differentiation. The physiological importance of Islet1 requires further study. Basic control of differentiation is similar in BAT but important differences include the effect of PGC-1α on mitochondrial biosynthesis and upregulation of UCP1; also PRDM16 plays a pivotal role in expression of the BAT phenotype. Modulation of the capacity or function of these different adipose tissue depots, by altering adipocyte differentiation or other means, holds promise for interventions that can be helpful in human disease, particularly cardiometabolic disorders associated with the world wide explosion of obesity. |
format | Online Article Text |
id | pubmed-4311677 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-43116772015-02-16 Control of Adipocyte Differentiation in Different Fat Depots; Implications for Pathophysiology or Therapy Ma, Xiuquan Lee, Paul Chisholm, Donald J. James, David E. Front Endocrinol (Lausanne) Endocrinology Adipocyte differentiation and its impact on restriction or expansion of particular adipose tissue depots have physiological and pathophysiological significance in view of the different functions of these depots. Brown or “beige” fat [brown adipose tissue (BAT)] expansion can enhance thermogenesis, lipid oxidation, insulin sensitivity, and glucose tolerance; conversely expanded visceral fat [visceral white adipose tissue (VAT)] is associated with insulin resistance, low grade inflammation, dyslipidemia, and cardiometabolic risk. The largest depot, subcutaneous white fat [subcutaneous white adipose tissue (SAT)], has important beneficial characteristics including storage of lipid “out of harms way” and secretion of adipokines, especially leptin and adiponectin, with positive metabolic effects including lipid oxidation, energy utilization, enhanced insulin action, and an anti-inflammatory role. The absence of these functions in lipodystrophies leads to major metabolic disturbances. An ability to expand white adipose tissue adipocyte differentiation would seem an important defense mechanism against the detrimental effects of energy excess and limit harmful accumulation of lipid in “ectopic” sites, such as liver and muscle. Adipocyte differentiation involves a transcriptional cascade with PPARγ being most important in SAT but less so in VAT, with increased angiogenesis also critical. The transcription factor, Islet1, is fairly specific to VAT and in vitro inhibits adipocyte differentiation. The physiological importance of Islet1 requires further study. Basic control of differentiation is similar in BAT but important differences include the effect of PGC-1α on mitochondrial biosynthesis and upregulation of UCP1; also PRDM16 plays a pivotal role in expression of the BAT phenotype. Modulation of the capacity or function of these different adipose tissue depots, by altering adipocyte differentiation or other means, holds promise for interventions that can be helpful in human disease, particularly cardiometabolic disorders associated with the world wide explosion of obesity. Frontiers Media S.A. 2015-01-30 /pmc/articles/PMC4311677/ /pubmed/25688231 http://dx.doi.org/10.3389/fendo.2015.00001 Text en Copyright © 2015 Ma, Lee, Chisholm and James. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Ma, Xiuquan Lee, Paul Chisholm, Donald J. James, David E. Control of Adipocyte Differentiation in Different Fat Depots; Implications for Pathophysiology or Therapy |
title | Control of Adipocyte Differentiation in Different Fat Depots; Implications for Pathophysiology or Therapy |
title_full | Control of Adipocyte Differentiation in Different Fat Depots; Implications for Pathophysiology or Therapy |
title_fullStr | Control of Adipocyte Differentiation in Different Fat Depots; Implications for Pathophysiology or Therapy |
title_full_unstemmed | Control of Adipocyte Differentiation in Different Fat Depots; Implications for Pathophysiology or Therapy |
title_short | Control of Adipocyte Differentiation in Different Fat Depots; Implications for Pathophysiology or Therapy |
title_sort | control of adipocyte differentiation in different fat depots; implications for pathophysiology or therapy |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4311677/ https://www.ncbi.nlm.nih.gov/pubmed/25688231 http://dx.doi.org/10.3389/fendo.2015.00001 |
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