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Granulocyte-colony stimulating factor for stroke treatment: mechanisms of action and efficacy in preclinical studies

G-CSF is widely employed for the treatment of chemotherapy-induced neutropenia. Recently, neuroprotective effects of G-CSF in animal stroke models were discovered including infarct size reduction and enhancement of functional recovery. The underlying mechanisms of action of G-CSF in ischemia appear...

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Autores principales: Minnerup, Jens, Sevimli, Sevgi, Schäbitz, Wolf-Rüdiger
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816868/
https://www.ncbi.nlm.nih.gov/pubmed/20142989
http://dx.doi.org/10.1186/2040-7378-1-2
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author Minnerup, Jens
Sevimli, Sevgi
Schäbitz, Wolf-Rüdiger
author_facet Minnerup, Jens
Sevimli, Sevgi
Schäbitz, Wolf-Rüdiger
author_sort Minnerup, Jens
collection PubMed
description G-CSF is widely employed for the treatment of chemotherapy-induced neutropenia. Recently, neuroprotective effects of G-CSF in animal stroke models were discovered including infarct size reduction and enhancement of functional recovery. The underlying mechanisms of action of G-CSF in ischemia appear to be a direct anti-apoptotic activity in neurons and a neurogenesis inducing capacity. Additional effects may be based on the stimulation of new blood-vessel formation, the stimulation of immunocompetence and -modulation as well as on bone marrow mobilization. In addition to a discussion of these mechanisms, we will review the available preclinical studies and analyze their impact on the overall efficacy of G-CSF in experimental stroke.
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spelling pubmed-28168682010-02-08 Granulocyte-colony stimulating factor for stroke treatment: mechanisms of action and efficacy in preclinical studies Minnerup, Jens Sevimli, Sevgi Schäbitz, Wolf-Rüdiger Exp Transl Stroke Med Review G-CSF is widely employed for the treatment of chemotherapy-induced neutropenia. Recently, neuroprotective effects of G-CSF in animal stroke models were discovered including infarct size reduction and enhancement of functional recovery. The underlying mechanisms of action of G-CSF in ischemia appear to be a direct anti-apoptotic activity in neurons and a neurogenesis inducing capacity. Additional effects may be based on the stimulation of new blood-vessel formation, the stimulation of immunocompetence and -modulation as well as on bone marrow mobilization. In addition to a discussion of these mechanisms, we will review the available preclinical studies and analyze their impact on the overall efficacy of G-CSF in experimental stroke. BioMed Central 2009-10-21 /pmc/articles/PMC2816868/ /pubmed/20142989 http://dx.doi.org/10.1186/2040-7378-1-2 Text en Copyright ©2009 Minnerup et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Minnerup, Jens
Sevimli, Sevgi
Schäbitz, Wolf-Rüdiger
Granulocyte-colony stimulating factor for stroke treatment: mechanisms of action and efficacy in preclinical studies
title Granulocyte-colony stimulating factor for stroke treatment: mechanisms of action and efficacy in preclinical studies
title_full Granulocyte-colony stimulating factor for stroke treatment: mechanisms of action and efficacy in preclinical studies
title_fullStr Granulocyte-colony stimulating factor for stroke treatment: mechanisms of action and efficacy in preclinical studies
title_full_unstemmed Granulocyte-colony stimulating factor for stroke treatment: mechanisms of action and efficacy in preclinical studies
title_short Granulocyte-colony stimulating factor for stroke treatment: mechanisms of action and efficacy in preclinical studies
title_sort granulocyte-colony stimulating factor for stroke treatment: mechanisms of action and efficacy in preclinical studies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816868/
https://www.ncbi.nlm.nih.gov/pubmed/20142989
http://dx.doi.org/10.1186/2040-7378-1-2
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