Cargando…

Mobilization of CD133(+) Progenitor Cells in Patients with Acute Cerebral Infarction

Progenitor cells (PCs) contribute to the endogenous repair mechanism after ischemic events. Interleukin-8 (IL-8) as part of the acute inflammatory reaction may enhance PC mobilization. Also, statins are supposed to alter number and function of circulating PCs. We aimed to investigate PC mobilization...

Descripción completa

Detalles Bibliográficos
Autores principales: Sepp, Dominik, Franz, Daniela, Triftshaeuser, Natalie, Ott, Ilka, Esposito-Bauer, Lorena, Feurer, Regina, Seifert, Christian L., Thaler, Markus, Hemmer, Bernhard, Poppert, Holger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3943863/
https://www.ncbi.nlm.nih.gov/pubmed/24599235
http://dx.doi.org/10.1371/journal.pone.0070796
_version_ 1782306311445151744
author Sepp, Dominik
Franz, Daniela
Triftshaeuser, Natalie
Ott, Ilka
Esposito-Bauer, Lorena
Feurer, Regina
Seifert, Christian L.
Thaler, Markus
Hemmer, Bernhard
Poppert, Holger
author_facet Sepp, Dominik
Franz, Daniela
Triftshaeuser, Natalie
Ott, Ilka
Esposito-Bauer, Lorena
Feurer, Regina
Seifert, Christian L.
Thaler, Markus
Hemmer, Bernhard
Poppert, Holger
author_sort Sepp, Dominik
collection PubMed
description Progenitor cells (PCs) contribute to the endogenous repair mechanism after ischemic events. Interleukin-8 (IL-8) as part of the acute inflammatory reaction may enhance PC mobilization. Also, statins are supposed to alter number and function of circulating PCs. We aimed to investigate PC mobilization after acute ischemic stroke as well as its association with inflammatory markers and statin therapy. Sixty-five patients with ischemic stroke were enrolled in the study. The number of CD133(+) PCs was analyzed by flow cytometry. Blood samples were drawn within 24 hours after symptom onset and after 5 days. The number of CD133(+) PCs increased significantly within 5 days (p<0.001). We found no correlation between CD133(+) PCs and the serum levels of IL-8, IL-6, or C-reactive protein (CRP). Multivariate analysis revealed that preexisting statin therapy correlated independently with the increase of CD133(+) PCs (p = 0.001). This study showed a mobilization of CD133(+) PCs in patients with acute cerebral infarction within 5 days after symptom onset. The early systemic inflammatory response did not seem to be a decisive factor in the mobilization of PCs. Preexisting statin therapy was associated with the increase in CD133(+) PCs, suggesting a potentially beneficial effect of statin therapy in patients with stroke.
format Online
Article
Text
id pubmed-3943863
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-39438632014-03-10 Mobilization of CD133(+) Progenitor Cells in Patients with Acute Cerebral Infarction Sepp, Dominik Franz, Daniela Triftshaeuser, Natalie Ott, Ilka Esposito-Bauer, Lorena Feurer, Regina Seifert, Christian L. Thaler, Markus Hemmer, Bernhard Poppert, Holger PLoS One Research Article Progenitor cells (PCs) contribute to the endogenous repair mechanism after ischemic events. Interleukin-8 (IL-8) as part of the acute inflammatory reaction may enhance PC mobilization. Also, statins are supposed to alter number and function of circulating PCs. We aimed to investigate PC mobilization after acute ischemic stroke as well as its association with inflammatory markers and statin therapy. Sixty-five patients with ischemic stroke were enrolled in the study. The number of CD133(+) PCs was analyzed by flow cytometry. Blood samples were drawn within 24 hours after symptom onset and after 5 days. The number of CD133(+) PCs increased significantly within 5 days (p<0.001). We found no correlation between CD133(+) PCs and the serum levels of IL-8, IL-6, or C-reactive protein (CRP). Multivariate analysis revealed that preexisting statin therapy correlated independently with the increase of CD133(+) PCs (p = 0.001). This study showed a mobilization of CD133(+) PCs in patients with acute cerebral infarction within 5 days after symptom onset. The early systemic inflammatory response did not seem to be a decisive factor in the mobilization of PCs. Preexisting statin therapy was associated with the increase in CD133(+) PCs, suggesting a potentially beneficial effect of statin therapy in patients with stroke. Public Library of Science 2014-03-05 /pmc/articles/PMC3943863/ /pubmed/24599235 http://dx.doi.org/10.1371/journal.pone.0070796 Text en © 2014 Sepp et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Sepp, Dominik
Franz, Daniela
Triftshaeuser, Natalie
Ott, Ilka
Esposito-Bauer, Lorena
Feurer, Regina
Seifert, Christian L.
Thaler, Markus
Hemmer, Bernhard
Poppert, Holger
Mobilization of CD133(+) Progenitor Cells in Patients with Acute Cerebral Infarction
title Mobilization of CD133(+) Progenitor Cells in Patients with Acute Cerebral Infarction
title_full Mobilization of CD133(+) Progenitor Cells in Patients with Acute Cerebral Infarction
title_fullStr Mobilization of CD133(+) Progenitor Cells in Patients with Acute Cerebral Infarction
title_full_unstemmed Mobilization of CD133(+) Progenitor Cells in Patients with Acute Cerebral Infarction
title_short Mobilization of CD133(+) Progenitor Cells in Patients with Acute Cerebral Infarction
title_sort mobilization of cd133(+) progenitor cells in patients with acute cerebral infarction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3943863/
https://www.ncbi.nlm.nih.gov/pubmed/24599235
http://dx.doi.org/10.1371/journal.pone.0070796
work_keys_str_mv AT seppdominik mobilizationofcd133progenitorcellsinpatientswithacutecerebralinfarction
AT franzdaniela mobilizationofcd133progenitorcellsinpatientswithacutecerebralinfarction
AT triftshaeusernatalie mobilizationofcd133progenitorcellsinpatientswithacutecerebralinfarction
AT ottilka mobilizationofcd133progenitorcellsinpatientswithacutecerebralinfarction
AT espositobauerlorena mobilizationofcd133progenitorcellsinpatientswithacutecerebralinfarction
AT feurerregina mobilizationofcd133progenitorcellsinpatientswithacutecerebralinfarction
AT seifertchristianl mobilizationofcd133progenitorcellsinpatientswithacutecerebralinfarction
AT thalermarkus mobilizationofcd133progenitorcellsinpatientswithacutecerebralinfarction
AT hemmerbernhard mobilizationofcd133progenitorcellsinpatientswithacutecerebralinfarction
AT poppertholger mobilizationofcd133progenitorcellsinpatientswithacutecerebralinfarction