Document Detail


Microvascular remodeling and wound healing: a role for pericytes.
MedLine Citation:
PMID:  22750474     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Physiologic wound healing is highly dependent on the coordinated functions of vascular and non-vascular cells. Resolution of tissue injury involves coagulation, inflammation, formation of granulation tissue, remodeling and scarring. Angiogenesis, the growth of microvessels the size of capillaries, is crucial for these processes, delivering blood-borne cells, nutrients and oxygen to actively remodeling areas. Central to angiogenic induction and regulation is microvascular remodeling, which is dependent upon capillary endothelial cell and pericyte interactions. Despite our growing knowledge of pericyte-endothelial cell crosstalk, it is unclear how the interplay among pericytes, inflammatory cells, glia and connective tissue elements shape microvascular injury response. Here, we consider the relationships that pericytes form with the cellular effectors of healing in normal and diabetic environments, including repair following injury and vascular complications of diabetes, such as diabetic macular edema and proliferative diabetic retinopathy. In addition, pericytes and stem cells possessing "pericyte-like" characteristics are gaining considerable attention in experimental and clinical efforts aimed at promoting healing or eradicating ocular vascular proliferative disorders. As the origin, identification and characterization of microvascular pericyte progenitor populations remains somewhat ambiguous, the molecular markers, structural and functional characteristics of pericytes will be briefly reviewed.
Authors:
Brian M Dulmovits; Ira M Herman
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Review     Date:  2012-06-28
Journal Detail:
Title:  The international journal of biochemistry & cell biology     Volume:  44     ISSN:  1878-5875     ISO Abbreviation:  Int. J. Biochem. Cell Biol.     Publication Date:  2012 Nov 
Date Detail:
Created Date:  2012-09-24     Completed Date:  2013-03-26     Revised Date:  2013-04-16    
Medline Journal Info:
Nlm Unique ID:  9508482     Medline TA:  Int J Biochem Cell Biol     Country:  Netherlands    
Other Details:
Languages:  eng     Pagination:  1800-12     Citation Subset:  IM    
Copyright Information:
Copyright © 2012 Elsevier Ltd. All rights reserved.
Affiliation:
Sackler School of Graduate Biomedical Sciences Program in Cellular and Molecular Physiology, Department of Molecular Physiology and Pharmacology and the Center for Innovation in Wound Healing Research, Tufts University, 150 Harrison Avenue, Boston, MA 02111, USA.
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MeSH Terms
Descriptor/Qualifier:
Animals
Diabetes Mellitus / pathology
Endothelial Cells / pathology*
Humans
Microvessels / pathology*
Pericytes / pathology*
Stem Cells / cytology
Wound Healing*
Grant Support
ID/Acronym/Agency:
19533//PHS HHS; NIH EY15125/EY/NEI NIH HHS; R01 EY015125/EY/NEI NIH HHS; R21 EY019553/EY/NEI NIH HHS

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