A method for culturing neonatal mice cardiomyocytes in vitro and its applications in toxicity evaluation
- VernacularTitle:新生小鼠心肌细胞培养模型的建立及其在毒性评价研究中的应用
- Author:
Hai-ying, YANG
;
Wei, DING
;
Ai-shi, DING
;
Shuang-qing, PENG
- Publication Type:Journal Article
- Keywords:
mice;
cardiomyocyte;
cell culture techniques;
immunohistochemistry
- From:Bulletin of The Academy of Military Medical Sciences
2010;34(1):30-33
- CountryChina
- Language:Chinese
-
Abstract:
Objective To establish a method for culturing neonatal mice cardiomyocytes, and construct an in vitro model of cardiomyocytes for assessing the cardiac toxicity of chemicals. Methods Hearts of neonatal mice of 1 day old were digested with enzyme mixture of trypsin/collagenase type Ⅱ/dispase and the cell suspensions were pre-plated to flask for a short time and then seeded on coated dishes. The cultured cells were treated with 5-fiuorine-deoxy-uridine(15 μg/ml)and uridine(35 μg/ml)to enrich cardiomyocytes that were identified according to the morphology and immunocytochemistry of α-actin antigen. Cardiac myocytes were incubated with 0-64 μg/ml of a fusarium mycotoxin butenolide(BUT) for 12 h. Cell viability was then evaluated by MTT assay. Microscopic observation showed that BUT induced significant morphological changes including cellular swelling, vacuolation and breakage of muscle fibers. Results It was found that 96% of the cultured cells were cardiomyocytes and the myocytes kept beating after 90 days of culture. Concentration-dependent decreases in cell viability following exposure of cardiac myocytes to BUT were observed. Conclusion The results indicated that relatively pure primary culture of neonatal mice cardiomyocytes is successfully established. BUT possesses the potential to induce myocardial toxicity.
