Modifications in rat plasma proteome after remote ischemic preconditioning (RIPC) stimulus: identification by a SELDI-TOF-MS approach.

Remote ischemic preconditioning's (RIPC) ability to render the myocardium resistant to subsequent prolonged ischemia is now clearly established in different species, including humans. Strong evidence suggests that circulating humoral mediators play a key role in signal transduction, but their i...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Pierre Hibert, Delphine Prunier-Mirebeau, Olivia Beseme, Maggy Chwastyniak, Sophie Tamareille, Florence Pinet, Fabrice Prunier
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2014
Materias:
R
Q
Acceso en línea:https://doaj.org/article/680bb896c25f4234902cdd023171749f
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:680bb896c25f4234902cdd023171749f
record_format dspace
spelling oai:doaj.org-article:680bb896c25f4234902cdd023171749f2021-11-18T08:37:54ZModifications in rat plasma proteome after remote ischemic preconditioning (RIPC) stimulus: identification by a SELDI-TOF-MS approach.1932-620310.1371/journal.pone.0085669https://doaj.org/article/680bb896c25f4234902cdd023171749f2014-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24454915/?tool=EBIhttps://doaj.org/toc/1932-6203Remote ischemic preconditioning's (RIPC) ability to render the myocardium resistant to subsequent prolonged ischemia is now clearly established in different species, including humans. Strong evidence suggests that circulating humoral mediators play a key role in signal transduction, but their identities still need to be established. Our study sought to identify potential circulating RIPC mediators using a proteomic approach. Rats were exposed to 10-min limb ischemia followed by 5- (RIPC 5') or 10-min (RIPC 10') reperfusion prior to blood sampling. The control group only underwent blood sampling. Plasma samples were isolated for proteomic analysis using surface-enhanced laser desorption and ionization - time of flight - mass spectrometry (SELDI-TOF-MS). A total of seven proteins, including haptoglobin and transthyretin, were detected as up- or down-regulated in response to RIPC. These proteins had previously been identified as associated with organ protection, anti-inflammation, and various cellular and molecular responses to ischemia. In conclusion, this study indicates that RIPC results in significant modulations of plasma proteome.Pierre HibertDelphine Prunier-MirebeauOlivia BesemeMaggy ChwastyniakSophie TamareilleFlorence PinetFabrice PrunierPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 9, Iss 1, p e85669 (2014)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Pierre Hibert
Delphine Prunier-Mirebeau
Olivia Beseme
Maggy Chwastyniak
Sophie Tamareille
Florence Pinet
Fabrice Prunier
Modifications in rat plasma proteome after remote ischemic preconditioning (RIPC) stimulus: identification by a SELDI-TOF-MS approach.
description Remote ischemic preconditioning's (RIPC) ability to render the myocardium resistant to subsequent prolonged ischemia is now clearly established in different species, including humans. Strong evidence suggests that circulating humoral mediators play a key role in signal transduction, but their identities still need to be established. Our study sought to identify potential circulating RIPC mediators using a proteomic approach. Rats were exposed to 10-min limb ischemia followed by 5- (RIPC 5') or 10-min (RIPC 10') reperfusion prior to blood sampling. The control group only underwent blood sampling. Plasma samples were isolated for proteomic analysis using surface-enhanced laser desorption and ionization - time of flight - mass spectrometry (SELDI-TOF-MS). A total of seven proteins, including haptoglobin and transthyretin, were detected as up- or down-regulated in response to RIPC. These proteins had previously been identified as associated with organ protection, anti-inflammation, and various cellular and molecular responses to ischemia. In conclusion, this study indicates that RIPC results in significant modulations of plasma proteome.
format article
author Pierre Hibert
Delphine Prunier-Mirebeau
Olivia Beseme
Maggy Chwastyniak
Sophie Tamareille
Florence Pinet
Fabrice Prunier
author_facet Pierre Hibert
Delphine Prunier-Mirebeau
Olivia Beseme
Maggy Chwastyniak
Sophie Tamareille
Florence Pinet
Fabrice Prunier
author_sort Pierre Hibert
title Modifications in rat plasma proteome after remote ischemic preconditioning (RIPC) stimulus: identification by a SELDI-TOF-MS approach.
title_short Modifications in rat plasma proteome after remote ischemic preconditioning (RIPC) stimulus: identification by a SELDI-TOF-MS approach.
title_full Modifications in rat plasma proteome after remote ischemic preconditioning (RIPC) stimulus: identification by a SELDI-TOF-MS approach.
title_fullStr Modifications in rat plasma proteome after remote ischemic preconditioning (RIPC) stimulus: identification by a SELDI-TOF-MS approach.
title_full_unstemmed Modifications in rat plasma proteome after remote ischemic preconditioning (RIPC) stimulus: identification by a SELDI-TOF-MS approach.
title_sort modifications in rat plasma proteome after remote ischemic preconditioning (ripc) stimulus: identification by a seldi-tof-ms approach.
publisher Public Library of Science (PLoS)
publishDate 2014
url https://doaj.org/article/680bb896c25f4234902cdd023171749f
work_keys_str_mv AT pierrehibert modificationsinratplasmaproteomeafterremoteischemicpreconditioningripcstimulusidentificationbyaselditofmsapproach
AT delphinepruniermirebeau modificationsinratplasmaproteomeafterremoteischemicpreconditioningripcstimulusidentificationbyaselditofmsapproach
AT oliviabeseme modificationsinratplasmaproteomeafterremoteischemicpreconditioningripcstimulusidentificationbyaselditofmsapproach
AT maggychwastyniak modificationsinratplasmaproteomeafterremoteischemicpreconditioningripcstimulusidentificationbyaselditofmsapproach
AT sophietamareille modificationsinratplasmaproteomeafterremoteischemicpreconditioningripcstimulusidentificationbyaselditofmsapproach
AT florencepinet modificationsinratplasmaproteomeafterremoteischemicpreconditioningripcstimulusidentificationbyaselditofmsapproach
AT fabriceprunier modificationsinratplasmaproteomeafterremoteischemicpreconditioningripcstimulusidentificationbyaselditofmsapproach
_version_ 1718421504886046720