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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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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2008
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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. |
format | Text |
id | pubmed-2276616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT hillsclairee intracellularsignallingbycpeptide AT brunskillnigelj intracellularsignallingbycpeptide |