Isolation, culture and CM-Dil labeling of rat mesenchymal stem cells in vitro
10.3969/j.issn.2095-4344.2014.01.007
- VernacularTitle:大鼠骨髓间充质干细胞体外分离培养与CM-DiI荧光标记
- Author:
Chaozhong LI
;
Jianming XIAO
;
Lixing CHEN
;
Wanrong LI
;
Chunhai ZHANG
- Publication Type:Journal Article
- Keywords:
Subject headings;
stem cells;
mesenchymal stem cells;
cells,cultured;
biological markers
- From:
Chinese Journal of Tissue Engineering Research
2014;(1):39-44
- CountryChina
- Language:Chinese
-
Abstract:
BACKGROUND:Currently, there is no uniform, standardized approach to isolate, purify and proliferate bone marrow mesenchymal stem cells. Chlormethylbenzamido-1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine (CM-Dil) is a stable, reliable, high marking and simple marker.
OBJECTIVE:To develop the methods for isolation, culture and identification of rat bone marrow mesenchymal stem cells in vitro.
METHODS:Two male Sprague-Dawley rats, weighing 50-100 g were taken to col ect the bilateral femur and tibia bone marrow under sterile conditions, and then, primary bone marrow mesenchymal stem cells were isolated and cultured using bone marrow adherent separation and density gradient centrifugation. cells were amplified and purified through timely and repeated passage, and labeled at the third generation with fluorescent dyes CM-Dil in vitro as a source of donor cells.
RESULTS AND CONCLUSION:Bone marrow mesenchymal stem cells were cultured successful y in vitro using bone marrow adherent separation and density gradient centrifugation separation methods, but the former was superior to the latter in the number of cultured cells significantly, while the two methods were not different significantly in terms of cellviability and proliferation. Flow cytometry results showed that the positive rates of cultured cells were 17.5%for CD34, 97.9%for CD44, and 91%for CD90. CM-Dil can label bone marrow mesenchymal stem cells successful y, which is a stable, reliable, high marking and simple marker.
