Effects of cobalt chloride-induced hypoxia on cell migration and expression and secretion of FSTL1 in melanoma cell line
10.11958/20150144
- VernacularTitle:氯化钴低氧对黑色素瘤细胞系迁移能力及FSTL1表达分泌的影响
- Author:
Fangyuan REN
;
Lian LI
;
Fangxin JIANG
;
Jing FENG
;
Baoyuan CHEN
;
Jie CAO
- Publication Type:Journal Article
- Keywords:
melanoma;
cell movement;
cell hypoxia;
cobalt chloride;
migration;
follistatin-like 1
- From:
Tianjin Medical Journal
2016;44(3):294-297
- CountryChina
- Language:Chinese
-
Abstract:
Objective To explore the effects of cobalt chloride (CoCl2)-induced hypoxia on migration of melanoma cells, and to detect the transcription, expression and secretion of Follistatin-like 1(FSTL1) in this process. Methods B16F10 melanoma cell line was treated with CoCl2 in order to mimic hypoxia. Experimental cells were divided into three groups: 0μmol/L, 50μmol/L and 100μmol/L CoCl2 treatment groups. MTT assay was used to assure cell viability, and to determine the treatment concentration of CoCl2. Transwell assay was used to determine the migration ability of B16F10 melanoma cell line. Real-time PCR was used to measure the mRNA expression of Fstl1. Western blot assay was used to detect the intracel?lular and extracellular protein expression of FSTL1. Results The cell viability of B16F10 melanoma cell line was signifi?cantly reduced by CoCl2 treatment, with a time and concentration-dependent manner. The migration ability of B16F10 cell line was significantly increased in CoCl2 treated group compared with that of control group (P<0.05). The mRNA level of Fstl1 was obviously higher in CoCl2 treated group than that of control group (P<0.05). The intracellular expression of FSTL1 protein was consistent with the expression trend of Fstl1 mRNA. Simultaneously, the extracellular protein level of FSTL1 was significantly decreased compared with that of control group. There was no expression of FSTL1 in 100μmol/L CoCl2 treat?ment group. Conclusion The migration ability of melanoma cell line is enhanced by CoCl2 treatment, which may be associ?ated with expression and secretion of FSTL1, however, the relevant mechanism still needs further investigation.
