Document Detail


Explant outgrowth, propagation and characterization of human pericytes.
MedLine Citation:
PMID:  20618694     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
OBJECTIVE: Pericytes are critical cellular components of the microvasculature that play a major role in vascular development and pathologies, yet their study has been hindered by lack of a standardized method for their isolation and growth. Here we report a method for culturing human pericytes from a readily available tissue source, placenta, and provide a thorough characterization of resultant cell populations.
METHODS: We developed an optimized protocol for obtaining pericytes by outgrowth from microvessel fragments recovered after enzymatic digestion of human placental tissue. We characterized outgrowth populations by immunostaining, by gene expression analysis, and by functional evaluation of cells implanted in vivo.
RESULTS: Our approach yields human pericytes that may be serially expanded in culture and that uniformly express the cellular markers NG2, CD90, CD146, alpha-SMA, and PDGFR-beta, but lack markers of smooth muscle cells, endothelial cells, and leukocytes. When co-implanted with human endothelial cells into C.B-17 SCID/bg mice, human pericytes invest and stabilize developing human endothelial cell-lined microvessels.
CONCLUSIONS: We conclude that our method for culturing pericytes from human placenta results in the expansion of functional pericytes that may be used to study a variety of questions related to vascular biology.
Authors:
Cheryl L Maier; Benjamin R Shepherd; Tai Yi; Jordan S Pober
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural    
Journal Detail:
Title:  Microcirculation (New York, N.Y. : 1994)     Volume:  17     ISSN:  1549-8719     ISO Abbreviation:  Microcirculation     Publication Date:  2010 Jul 
Date Detail:
Created Date:  2010-07-12     Completed Date:  2010-10-29     Revised Date:  2012-03-15    
Medline Journal Info:
Nlm Unique ID:  9434935     Medline TA:  Microcirculation     Country:  United States    
Other Details:
Languages:  eng     Pagination:  367-80     Citation Subset:  IM    
Affiliation:
Departments of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06520, USA.
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MeSH Terms
Descriptor/Qualifier:
Animals
Biological Markers / metabolism
Capillary Permeability
Cell Culture Techniques / methods*
Cell Separation
Endothelial Cells / transplantation
Female
Gene Expression Profiling
Humans
Immunophenotyping
Mice
Mice, SCID
Microvessels / cytology
Myocytes, Smooth Muscle / cytology
Oligonucleotide Array Sequence Analysis
Pericytes / cytology*,  physiology*,  transplantation
Placenta / blood supply,  cytology
Pregnancy
Transplantation, Heterologous
Grant Support
ID/Acronym/Agency:
R01 HL051014-17/HL/NHLBI NIH HHS; R01 HL085416-05/HL/NHLBI NIH HHS; R01 HL085416-07/HL/NHLBI NIH HHS; R01-HL051014/HL/NHLBI NIH HHS; R01-HL085416/HL/NHLBI NIH HHS; T32-GM-007205/GM/NIGMS NIH HHS
Chemical
Reg. No./Substance:
0/Biological Markers
Comments/Corrections

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