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Lipolysis: more than just a lipase

Successful adaptation to starvation in mammals depends heavily on the regulated mobilization of fatty acids from triacylglycerols stored in adipose tissue. Although it has long been recognized that cyclic AMP represents the critical second messenger and hormone-sensitive lipase (HSL) the rate-determ...

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Detalles Bibliográficos
Autor principal: Birnbaum, Morris J.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172981/
https://www.ncbi.nlm.nih.gov/pubmed/12810703
http://dx.doi.org/10.1083/jcb.200306008
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author Birnbaum, Morris J.
author_facet Birnbaum, Morris J.
author_sort Birnbaum, Morris J.
collection PubMed
description Successful adaptation to starvation in mammals depends heavily on the regulated mobilization of fatty acids from triacylglycerols stored in adipose tissue. Although it has long been recognized that cyclic AMP represents the critical second messenger and hormone-sensitive lipase (HSL) the rate-determining enzyme for lipolysis, simple activation of the enzyme has failed to account for the robust augmentation of fatty release in response to physiological agonists. In this issue, Sztalryd et al. (2003) provide convincing support to the notion that the subcellular compartmentalization of lipase also regulates lipolysis, and, more importantly, that proteins other than HSL are localized to the lipid droplet and are indispensable for its optimal hydrolysis.
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spelling pubmed-21729812008-05-01 Lipolysis: more than just a lipase Birnbaum, Morris J. J Cell Biol Comment Successful adaptation to starvation in mammals depends heavily on the regulated mobilization of fatty acids from triacylglycerols stored in adipose tissue. Although it has long been recognized that cyclic AMP represents the critical second messenger and hormone-sensitive lipase (HSL) the rate-determining enzyme for lipolysis, simple activation of the enzyme has failed to account for the robust augmentation of fatty release in response to physiological agonists. In this issue, Sztalryd et al. (2003) provide convincing support to the notion that the subcellular compartmentalization of lipase also regulates lipolysis, and, more importantly, that proteins other than HSL are localized to the lipid droplet and are indispensable for its optimal hydrolysis. The Rockefeller University Press 2003-06-23 /pmc/articles/PMC2172981/ /pubmed/12810703 http://dx.doi.org/10.1083/jcb.200306008 Text en Copyright © 2003, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Comment
Birnbaum, Morris J.
Lipolysis: more than just a lipase
title Lipolysis: more than just a lipase
title_full Lipolysis: more than just a lipase
title_fullStr Lipolysis: more than just a lipase
title_full_unstemmed Lipolysis: more than just a lipase
title_short Lipolysis: more than just a lipase
title_sort lipolysis: more than just a lipase
topic Comment
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172981/
https://www.ncbi.nlm.nih.gov/pubmed/12810703
http://dx.doi.org/10.1083/jcb.200306008
work_keys_str_mv AT birnbaummorrisj lipolysismorethanjustalipase