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Bone marrow Derived Pluripotent Cells are Pericytes which Contribute to Vascularization

Cai, Xiaoxiao; Lin, Yunfeng; Friedrich, Claudia C; Neville, Craig; Pomerantseva, Irina; Sundback, Cathryn A; Sharma, Parul; Zhang, Zhiyuan; Vacanti, Joseph P; Hauschka, Peter V; Grottkau, Brian E (2009). Bone marrow Derived Pluripotent Cells are Pericytes which Contribute to Vascularization. Stem Cell Reviews, 5(4):437-445.

Abstract

Pericytes are essential to vascularization, but the purification and characterization of pericytes remain unclear. Smooth muscle actin alpha (α-SMA) is one maker of pericytes. The aim of this study is to purify the α-SMA positive cells from bone marrow and study the characteristics of these cells and the interaction between α-SMA positive cells and endothelial cells. The bone marrow stromal cells were harvested from α-SMA-GFP transgenic mice, and the α-SMA-GFP positive cells were sorted by FACS. The proliferative characteristics and multilineage differentiation ability of the α-SMA-GFP positive cells were tested. A 3-D culture model was then applied to test their vascularization by loading α-SMA-GFP positive cells and endothelial cells on collagen-fibronectin gel. Results demonstrated that bone marrow stromal cells are mostly α-SMA-GFP positive cells which are pluripotent, and these cells expressed α-SMA during differentiation. The α-SMA-GFP positive cells could stimulate the endothelial cells to form tube-like structures and subsequently robust vascular networks in 3-D culture. In conclusion, the bone marrow derived pluripotent cells are pericytes and can contribute to vascularization.

Additional indexing

Item Type:Journal Article, refereed, original work
Communities & Collections:04 Faculty of Medicine > University Hospital Zurich > Institute of Intensive Care Medicine
Dewey Decimal Classification:610 Medicine & health
Scopus Subject Areas:Life Sciences > Cell Biology
Life Sciences > Cancer Research
Uncontrolled Keywords:Cancer Research, Cell Biology
Language:English
Date:1 December 2009
Deposited On:29 Nov 2021 07:58
Last Modified:26 Dec 2024 02:38
Publisher:Springer
ISSN:1550-8943
OA Status:Closed
Publisher DOI:https://doi.org/10.1007/s12015-009-9097-6
PubMed ID:20058207

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