Changes in apoptosis-related genes in bone marrow mesenchymal stem cells after cocultured with hepatic stellate cells
10.3969/j.issn.2095-4344.2014.28.003
- VernacularTitle:骨髓间充质干细胞与肝星状细胞共培养后凋亡相关基因的改变
- Author:
Kunpeng HU
;
Bo LIU
;
Zhicheng YAO
;
Jizong LIN
;
Meihai DENG
;
Weidong PAN
;
Nan LIN
;
Cheng CHEN
;
Ruiyun XU
- Publication Type:Journal Article
- Keywords:
bone marrow;
mesenchymal stem cells;
hepatic stel ate cells;
apoptosis;
microchip analytical procedures
- From:
Chinese Journal of Tissue Engineering Research
2014;(28):4444-4449
- CountryChina
- Language:Chinese
-
Abstract:
BACKGROUND:Previous studies have confirmed that bone marrow mesenchymal stem cells in vitro can promote hepatic stel ate cellapoptosis and inhibit its activity, in which the mechanism of action remains unknown. OBJECTIVE:To screen out apoptosis-related genes during hepatic stel ate cellapoptosis regulated by bone marrow mesenchymal stem cells using gene chip technology. METHODS:Purified human bone marrow mesenchymal stem cells were seeded in 6-wel Transwel plate and cocultured with hepatic stel ate cells. Cultured human bone marrow mesenchymal stem cells alone served as control group, and cultured for 72 hours. The alterations in apoptosis-related genes were analyzed between culture alone group and coculture group using gene chip technology. The genes strongly associated with regulation of hepatic stel ate cells were selected. RESULTS AND CONCLUSION:By the functional classification of second-generation SABiosciences Gene chips, apoptotic gene screening found that after coculture, significantly upregulated genes in bone marrow mesenchymal stem cells contained:AKT1, PIK3R2, DAPK1, DHCR24, NOTCH2 and BDNF. Combined with previous findings, we hypothesized that NOTCH may play a key role in the regulation of hepatic stel ate cells by bone marrow mesenchymal stem cells.
