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Intracellular Signalling by C-Peptide

C-peptide, a cleavage product of the proinsulin molecule, has long been regarded as biologically inert, serving merely as a surrogate marker for insulin release. Recent findings demonstrate both a physiological and protective role of C-peptide when administered to individuals with type I diabetes. D...

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Detalles Bibliográficos
Autores principales: Hills, Claire E., Brunskill, Nigel J.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2276616/
https://www.ncbi.nlm.nih.gov/pubmed/18382618
http://dx.doi.org/10.1155/2008/635158
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author Hills, Claire E.
Brunskill, Nigel J.
author_facet Hills, Claire E.
Brunskill, Nigel J.
author_sort Hills, Claire E.
collection PubMed
description C-peptide, a cleavage product of the proinsulin molecule, has long been regarded as biologically inert, serving merely as a surrogate marker for insulin release. Recent findings demonstrate both a physiological and protective role of C-peptide when administered to individuals with type I diabetes. Data indicate that C-peptide appears to bind in nanomolar concentrations to a cell surface receptor which is most likely to be G-protein coupled. Binding of C-peptide initiates multiple cellular effects, evoking a rise in intracellular calcium, increased PI-3-kinase activity, stimulation of the Na(+)/K(+) ATPase, increased eNOS transcription, and activation of the MAPK signalling pathway. These cell signalling effects have been studied in multiple cell types from multiple tissues. Overall these observations raise the possibility that C-peptide may serve as a potential therapeutic agent for the treatment or prevention of long-term complications associated with diabetes.
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spelling pubmed-22766162008-04-01 Intracellular Signalling by C-Peptide Hills, Claire E. Brunskill, Nigel J. Exp Diabetes Res Review Article C-peptide, a cleavage product of the proinsulin molecule, has long been regarded as biologically inert, serving merely as a surrogate marker for insulin release. Recent findings demonstrate both a physiological and protective role of C-peptide when administered to individuals with type I diabetes. Data indicate that C-peptide appears to bind in nanomolar concentrations to a cell surface receptor which is most likely to be G-protein coupled. Binding of C-peptide initiates multiple cellular effects, evoking a rise in intracellular calcium, increased PI-3-kinase activity, stimulation of the Na(+)/K(+) ATPase, increased eNOS transcription, and activation of the MAPK signalling pathway. These cell signalling effects have been studied in multiple cell types from multiple tissues. Overall these observations raise the possibility that C-peptide may serve as a potential therapeutic agent for the treatment or prevention of long-term complications associated with diabetes. Hindawi Publishing Corporation 2008 2008-03-18 /pmc/articles/PMC2276616/ /pubmed/18382618 http://dx.doi.org/10.1155/2008/635158 Text en Copyright © 2008 C. E. Hills and N. J. Brunskill. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Hills, Claire E.
Brunskill, Nigel J.
Intracellular Signalling by C-Peptide
title Intracellular Signalling by C-Peptide
title_full Intracellular Signalling by C-Peptide
title_fullStr Intracellular Signalling by C-Peptide
title_full_unstemmed Intracellular Signalling by C-Peptide
title_short Intracellular Signalling by C-Peptide
title_sort intracellular signalling by c-peptide
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2276616/
https://www.ncbi.nlm.nih.gov/pubmed/18382618
http://dx.doi.org/10.1155/2008/635158
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