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Vascular Wall-Resident CD44+Multipotent Stem Cells Give Rise to Pericytes and Smooth Muscle Cells and Contribute to New Vessel Maturation
被引:129
|作者:
Klein, Diana
[1
]
Weisshardt, Philip
[1
]
Kleff, Veronika
[1
]
Jastrow, Holger
[1
]
Jakob, Heinz Guenther
[2
]
Erguen, Sueleyman
[1
]
机构:
[1] Univ Hosp Essen, Inst Anat, Essen, N Rhine Westpha, Germany
[2] Univ Hosp Essen, Clin Thorax & Cardiovasc Surg, Essen, N Rhine Westpha, Germany
来源:
PLOS ONE
|
2011年
/
6卷
/
05期
关键词:
PERIVASCULAR PROGENITOR CELLS;
MESENCHYMAL STROMAL CELLS;
ENDOTHELIAL-CELLS;
GROWTH-FACTOR;
ANGIOGENESIS;
CANCER;
D O I:
10.1371/journal.pone.0020540
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Here, we identify CD44(+)CD90(+)CD73(-)CD34(-)CD45(-) cells within the adult human arterial adventitia with properties of multipotency which were named vascular wall-resident multipotent stem cells (VW-MPSCs). VW-MPSCs exhibit typical mesenchymal stem cell characteristics including cell surface markers in immunostaining and flow cytometric analyses, and differentiation into adipocytes, chondrocytes and osteocytes under culture conditions. Particularly, TGF beta 1 stimulation up-regulates smooth muscle cell markers in VW-MPSCs. Using fluorescent cell labelling and co-localisation studies we show that VW-MPSCs differentiate to pericytes/smooth muscle cells which cover the wall of newly formed endothelial capillary-like structures in vitro. Co-implantation of EGFP-labelled VW-MPSCs and human umbilical vein endothelial cells into SCID mice subcutaneously via Matrigel results in new vessels formation which were covered by pericyte-or smooth muscle-like cells generated from implanted VW-MPSCs. Our results suggest that VW-MPSCs are of relevance for vascular morphogenesis, repair and self-renewal of vascular wall cells and for local capacity of neovascularization in disease processes.
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