In vitro endothelial potential of human UC blood-derived mesenchymal stem cells

被引:89
作者
Gang, E. J.
Jeong, J. A.
Han, S.
Yan, Q.
Jeon, C-J
Kim, H.
机构
[1] Creagene Co, Creagene Res Inst, Seoul 135960, South Korea
[2] Histostem Co, Biotechnol Res Inst, Seoul, South Korea
关键词
endothelial differentiation; human umbilical cord blood; mesenchymal stem cells;
D O I
10.1080/14653240600735933
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background Human mesenchymal stem cells (MSC) possess powerful ex vivo expansion and versatile differentiation potential, placing themselves at the forefront of the field of stem cell-based therapy and transplantation. Of high clinical relevance is the endothelial differentiation potential of MSC, which can be used to treat various forms of ischemic vascular disease. Methods We investigated whether human umbilical cord blood (UCB)-derived MSC are able to differentiate in vitro along an endothelial lineage, by using flow cytometry, RT-PCR and immunofluorescence analyzes, as well as an Ab array method. Results When the cells were incubated for up to 3 weeks in the presence of VEGF, EGF and hydrocortisone, they began to express a variety of endothelial lineage surface markers, such as Flk-1, Flt-1, VE-Cadherin, vWF, VCAM-1, Tie-1 and Tie-2, and to secrete a specific set of cytokines. Differentiated cells were also found to be able to uptake low-density lipoprotein and form a tubular network structure. Discussion These observations have led us to conclude that UCB-derived MSC retain endothelial potential that is suitable for basic and clinical studies aimed at the development of vasculature-directed regenerative medicine.
引用
收藏
页码:215 / 227
页数:13
相关论文
共 69 条
[11]  
2-C
[12]   Mesenchymal progenitor cells differentiate into an endothelial phenotype, enhance vascular density, and improve heart function in a rat cellular cardiomyoplasty model [J].
Davani, S ;
Marandin, A ;
Mersin, N ;
Royer, B ;
Kantelip, B ;
Hervé, P ;
Etievent, JP ;
Kantelip, JP .
CIRCULATION, 2003, 108 (10) :253-258
[13]   Young adult bone marrow-derived endothelial precursor cells restore aging-impaired cardiac angiogenic function [J].
Edelberg, JM ;
Tang, LL ;
Hattori, K ;
Lyden, D ;
Rafii, S .
CIRCULATION RESEARCH, 2002, 90 (10) :E89-E93
[14]   Endothelial progenitor cell culture and differentiation in vitro: a methodological comparison using human umbilical cord blood [J].
Eggermann, J ;
Kliche, S ;
Jarmy, G ;
Hoffmann, K ;
Mayr-Beyrle, U ;
Debatin, KM ;
Waltenberger, J ;
Beltinger, C .
CARDIOVASCULAR RESEARCH, 2003, 58 (02) :478-486
[15]   Mesenchymal progenitor cells in human umbilical cord blood [J].
Erices, A ;
Conget, P ;
Minguell, JJ .
BRITISH JOURNAL OF HAEMATOLOGY, 2000, 109 (01) :235-242
[16]   Vascular endothelial growth factor: Basic science and clinical progress [J].
Ferrara, N .
ENDOCRINE REVIEWS, 2004, 25 (04) :581-611
[17]   ROLE OF THE FLT-1 RECEPTOR TYROSINE KINASE IN REGULATING THE ASSEMBLY OF VASCULAR ENDOTHELIUM [J].
FONG, GH ;
ROSSANT, J ;
GERTSENSTEIN, M ;
BREITMAN, ML .
NATURE, 1995, 376 (6535) :66-70
[18]   Growth factors acting via endothelial cell-specific receptor tyrosine kinases: VEGFs, angiopoietins, and ephrins in vascular development [J].
Gale, NW ;
Yancopoulos, GD .
GENES & DEVELOPMENT, 1999, 13 (09) :1055-1066
[19]   In vitro mesengenic potential of human umbilical cord blood-derived mesenchymal stem cells [J].
Gang, EJ ;
Hong, SH ;
Jeong, JA ;
Hwang, SH ;
Kim, SW ;
Yang, IH ;
Ahn, CY ;
Han, H ;
Kim, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 321 (01) :102-108
[20]   Skeletal myogenic differentiation of mesenchymal stem cells isolated from human umbilical cord blood [J].
Gang, EJ ;
Jeong, JA ;
Hong, SH ;
Hwang, SH ;
Kim, SW ;
Yang, IH ;
Ahn, C ;
Han, H ;
Kim, H .
STEM CELLS, 2004, 22 (04) :617-624