Myocardin-related transcription factor A regulates conversion of progenitors to beige adipocytes

Thermogenic brown adipose tissue generates heat via mitochondrial uncoupling protein-1 (UCP-1), increases whole-body energy expenditure and may protects against obesity and metabolic disorders. White adipocytes store excess energy in the form of triglycerides. UCP-1 positive adipocytes develop withi...

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Main Author: Li, Chendi
Language:en_US
Published: 2016
Subjects:
Online Access:https://hdl.handle.net/2144/16110
id ndltd-bu.edu-oai-open.bu.edu-2144-16110
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spelling ndltd-bu.edu-oai-open.bu.edu-2144-161102019-03-26T06:42:22Z Myocardin-related transcription factor A regulates conversion of progenitors to beige adipocytes Li, Chendi Biochemistry Beige adipocyte MRTFA UCP-1 Whole-body metabolism Thermogenic brown adipose tissue generates heat via mitochondrial uncoupling protein-1 (UCP-1), increases whole-body energy expenditure and may protects against obesity and metabolic disorders. White adipocytes store excess energy in the form of triglycerides. UCP-1 positive adipocytes develop within white adipose tissue (beige or brite adipocytes) in response to cold exposure or β3 adrenergic agonists. It was known that beige adipocytes arise from a distinct lineage compared with brown adipocytes, but the developmental origin of the beige adipocytes is still unclear. Signaling pathways that control beige adipocyte determination and formation are essentially unknown. Here, we identified a novel signaling pathway that regulates the lineage specification of beige adipocytes. Bone morphogenetic protein 7 (BMP7), a known brown adipogenesis inducer, suppresses Rho-GTPase kinase (ROCK) and depolymerizes F-actin (filamentous actin) into G-actin (globular actin) in mesenchymal stem cells. G-actin regulates myocardin-related transcription factor A (MRTFA) that co-transactivates serum response factor (SRF) and promotes smooth muscle cell differentiation in various organs. Subcutaneous white adipose tissue from MRTFA-/- mice had enhanced accumulation of UCP-1+ adipocytes and elevated levels of brown-selective proteins. Compared with wild type (WT) controls, MRTFA-/- mice exhibited improved metabolic profiles and were protected from diet-induced obesity and insulin resistance, suggesting that the beige adipocytes are physiologically functional. Compared to WT mice, stromal vascular cells from MRTFA-/- mice expressed higher levels of distinct beige progenitor markers and reduced levels of smooth muscle markers. Our studies demonstrate a novel ROCK-actin-MRTFA/SRF pathway that contributes to the development of beige adipocytes. 2016-04-27T19:07:01Z 2016-04-27T19:07:01Z 2015 2016-04-08T20:15:55Z Thesis/Dissertation https://hdl.handle.net/2144/16110 en_US
collection NDLTD
language en_US
sources NDLTD
topic Biochemistry
Beige adipocyte
MRTFA
UCP-1
Whole-body metabolism
spellingShingle Biochemistry
Beige adipocyte
MRTFA
UCP-1
Whole-body metabolism
Li, Chendi
Myocardin-related transcription factor A regulates conversion of progenitors to beige adipocytes
description Thermogenic brown adipose tissue generates heat via mitochondrial uncoupling protein-1 (UCP-1), increases whole-body energy expenditure and may protects against obesity and metabolic disorders. White adipocytes store excess energy in the form of triglycerides. UCP-1 positive adipocytes develop within white adipose tissue (beige or brite adipocytes) in response to cold exposure or β3 adrenergic agonists. It was known that beige adipocytes arise from a distinct lineage compared with brown adipocytes, but the developmental origin of the beige adipocytes is still unclear. Signaling pathways that control beige adipocyte determination and formation are essentially unknown. Here, we identified a novel signaling pathway that regulates the lineage specification of beige adipocytes. Bone morphogenetic protein 7 (BMP7), a known brown adipogenesis inducer, suppresses Rho-GTPase kinase (ROCK) and depolymerizes F-actin (filamentous actin) into G-actin (globular actin) in mesenchymal stem cells. G-actin regulates myocardin-related transcription factor A (MRTFA) that co-transactivates serum response factor (SRF) and promotes smooth muscle cell differentiation in various organs. Subcutaneous white adipose tissue from MRTFA-/- mice had enhanced accumulation of UCP-1+ adipocytes and elevated levels of brown-selective proteins. Compared with wild type (WT) controls, MRTFA-/- mice exhibited improved metabolic profiles and were protected from diet-induced obesity and insulin resistance, suggesting that the beige adipocytes are physiologically functional. Compared to WT mice, stromal vascular cells from MRTFA-/- mice expressed higher levels of distinct beige progenitor markers and reduced levels of smooth muscle markers. Our studies demonstrate a novel ROCK-actin-MRTFA/SRF pathway that contributes to the development of beige adipocytes.
author Li, Chendi
author_facet Li, Chendi
author_sort Li, Chendi
title Myocardin-related transcription factor A regulates conversion of progenitors to beige adipocytes
title_short Myocardin-related transcription factor A regulates conversion of progenitors to beige adipocytes
title_full Myocardin-related transcription factor A regulates conversion of progenitors to beige adipocytes
title_fullStr Myocardin-related transcription factor A regulates conversion of progenitors to beige adipocytes
title_full_unstemmed Myocardin-related transcription factor A regulates conversion of progenitors to beige adipocytes
title_sort myocardin-related transcription factor a regulates conversion of progenitors to beige adipocytes
publishDate 2016
url https://hdl.handle.net/2144/16110
work_keys_str_mv AT lichendi myocardinrelatedtranscriptionfactoraregulatesconversionofprogenitorstobeigeadipocytes
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