Isolation, characterisation and comparative analysis of human umbilical cord vein perivascular cells and cord blood mesenchymal stem cells

被引:18
作者
Gokcinar-Yagei, Beyza [1 ,2 ]
Ozyuncu, Ozgur [3 ]
Celebi-Saltik, Betul [1 ,2 ]
机构
[1] Hacettepe Univ, Grad Sch Hlth Sci, Dept Stem Cell Sci, TR-06100 Ankara, Turkey
[2] Hacettepe Univ, Ctr Stem Cell Res & Dev, TR-06100 Ankara, Turkey
[3] Hacettepe Univ, Dept Obstet & Gynecol, Fac Med, TR-06100 Ankara, Turkey
关键词
Perivascular cells; Umbilical cord; Vein; CD146; Mesenchymal stem cells; SMOOTH-MUSCLE-CELLS; EX-VIVO EXPANSION; BONE-MARROW; TENASCIN-C; MICROVASCULAR PERICYTES; STROMAL CELLS; ALPHA-ACTIN; HUMAN FETAL; IN-VITRO; EXPRESSION;
D O I
10.1007/s10561-015-9542-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Perivascular cells are known to be ancestors of mesenchymal stem cells (MSCs) and can be obtained from heart, skin, bone marrow, eye, placenta and umbilical cord (UC). However detailed characterization of perivascular cells around the human UC vein and comparative analysis of them with MSCs haven't been done yet. In this study, our aim is to isolate perivascular cells from human UC vein and characterize them versus UC blood MSCs (UCB-MSCs). For this purpose, perivascular cells around the UC vein were isolated enzymatically and then purified with magnetic activated cell sorting (MACS) method using CD146 Microbead Kit respectively. MSCs were isolated from UCB by Ficoll density gradient solution. Perivascular cells and UCB-MSCs were characterized by osteogenic and adipogenic differentiation procedures, flow cytometric analysis [CD146, CD105, CD31, CD34, CD45 and alpha-smooth muscle actin (alpha-SMA)], and immunofluorescent staining (MAP1B and Tenascin C). Alizarin red and Oil red O staining results showed that perivascular cells and MSCs had osteogenic and adipogenic differentiation capacity. However, osteogenic differentiation capacity of perivascular cells were found to be less than UCB-MSCs. According to flow cytometric analysis, CD146 expression of perivascular cells were appeared to be 4.8-fold higher than UCB-MSCs. Expression of alpha-SMA, MAP1B and Tenascin-C from perivascular cells was determined by flow cytometry analysis and immunfluorescent staining. The results appear to support the fact that perivascular cells are the ancestors of MSCs in vascular area. They may be used as alternative cells to MSCs in the field of vascular tissue engineering.
引用
收藏
页码:345 / 352
页数:8
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