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Regulation of ceramide channel formation and disassembly: Insights on the initiation of apoptosis

Sphingolipid research has surged in the past two decades and has produced a wide variety of evidence supporting the role of this class of molecules in mediating cellular growth, differentiation, senescence, and apoptosis. Ceramides are a subgroup of sphingolipids (SLs) that are directly involved in...

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Detalles Bibliográficos
Autores principales: Abou-Ghali, Majdouline, Stiban, Johnny
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4625378/
https://www.ncbi.nlm.nih.gov/pubmed/26587005
http://dx.doi.org/10.1016/j.sjbs.2015.03.005
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author Abou-Ghali, Majdouline
Stiban, Johnny
author_facet Abou-Ghali, Majdouline
Stiban, Johnny
author_sort Abou-Ghali, Majdouline
collection PubMed
description Sphingolipid research has surged in the past two decades and has produced a wide variety of evidence supporting the role of this class of molecules in mediating cellular growth, differentiation, senescence, and apoptosis. Ceramides are a subgroup of sphingolipids (SLs) that are directly involved in the process of initiation of apoptosis. We, and others, have recently shown that ceramides are capable of the formation of protein-permeable channels in mitochondrial outer membranes under physiological conditions. These pores are indeed good candidates for the pathway of release of pro-apoptotic proteins from the mitochondrial intermembrane space (IMS) into the cytosol to initiate intrinsic apoptosis. Here, we review recent findings on the regulation of ceramide channel formation and disassembly, highlighting possible implications on the initiation of the intrinsic apoptotic pathway.
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spelling pubmed-46253782015-11-19 Regulation of ceramide channel formation and disassembly: Insights on the initiation of apoptosis Abou-Ghali, Majdouline Stiban, Johnny Saudi J Biol Sci Original Article Sphingolipid research has surged in the past two decades and has produced a wide variety of evidence supporting the role of this class of molecules in mediating cellular growth, differentiation, senescence, and apoptosis. Ceramides are a subgroup of sphingolipids (SLs) that are directly involved in the process of initiation of apoptosis. We, and others, have recently shown that ceramides are capable of the formation of protein-permeable channels in mitochondrial outer membranes under physiological conditions. These pores are indeed good candidates for the pathway of release of pro-apoptotic proteins from the mitochondrial intermembrane space (IMS) into the cytosol to initiate intrinsic apoptosis. Here, we review recent findings on the regulation of ceramide channel formation and disassembly, highlighting possible implications on the initiation of the intrinsic apoptotic pathway. Elsevier 2015-11 2015-03-22 /pmc/articles/PMC4625378/ /pubmed/26587005 http://dx.doi.org/10.1016/j.sjbs.2015.03.005 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Abou-Ghali, Majdouline
Stiban, Johnny
Regulation of ceramide channel formation and disassembly: Insights on the initiation of apoptosis
title Regulation of ceramide channel formation and disassembly: Insights on the initiation of apoptosis
title_full Regulation of ceramide channel formation and disassembly: Insights on the initiation of apoptosis
title_fullStr Regulation of ceramide channel formation and disassembly: Insights on the initiation of apoptosis
title_full_unstemmed Regulation of ceramide channel formation and disassembly: Insights on the initiation of apoptosis
title_short Regulation of ceramide channel formation and disassembly: Insights on the initiation of apoptosis
title_sort regulation of ceramide channel formation and disassembly: insights on the initiation of apoptosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4625378/
https://www.ncbi.nlm.nih.gov/pubmed/26587005
http://dx.doi.org/10.1016/j.sjbs.2015.03.005
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