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砷对大鼠肢芽细胞增殖和分化的影响
引用本文:李勇 孔佩艳. 砷对大鼠肢芽细胞增殖和分化的影响[J]. 卫生研究, 1998, 27(3): 161-163
作者姓名:李勇 孔佩艳
作者单位:上海医科大学环境卫生教研室(李勇),第三军医大学(朱惠刚),北京医科大学中国妇婴保健中心(孔佩艳)
基金项目:国家教委博士后科学基金
摘    要:
为了进一步阐明三氧化二砷的发育毒性,本研究应用Flint等人建立的胚胎肢芽细胞微团培养法,探讨了不同浓度砷对体外培养的SD大鼠胚胎肢芽细胞增殖和分化的影响。结果表明砷对大鼠肢芽细胞的增殖和分化均有抑制作用,呈明显的剂量-反应关系;砷对肢芽细胞的50%增殖抑制浓度(IP50)和50%分化抑制浓度(ID50)分别为0.70mg/L和0.21mg/L;IP50/ID50值为3.3,揭示砷对大鼠肢芽细胞分化的影响要远大于对细胞增殖的影响。根据Renault等人推荐的体外致畸判断标准,砷属于强致畸物。实验结果提示砷对大鼠肢芽细胞分化的抑制作用可能并非其细胞毒性作用所致,这是砷致畸作用的重要基础之一。此外还初步探讨了大鼠肢芽细胞异常分化的分子机制。

关 键 词:肢芽细胞  微团培养  分化  增殖  三氧化二砷  致畸性

Influence of Arsenic on Proliferation and Differentiation of Rat Bud Cells in Vitro
Y Li,H Zhu,P Kong. Influence of Arsenic on Proliferation and Differentiation of Rat Bud Cells in Vitro[J]. Journal of hygiene research, 1998, 27(3): 161-163
Authors:Y Li  H Zhu  P Kong
Affiliation:Department of Environmental Health, Shanghai Medical University, China.
Abstract:
The objective of this study was designed to evaluate the developmental toxicity of arsenic and its effect on embryonic chondrogenesis of Sprague-Dawley rat by using Flint's rat limb bud cell micromass cultrure system in vitro. The results revealed that arsenic inhibited markedly both proliferation and differentiation of rat limb bud cells in vitro and there was an obvious dose-response relationship. The concentrations of arsenic for IP50(dose of inhibiting proliferation by 50% of the control value) and ID50(dose of inhibiting differentiation by 50% of the control value) were 0.70 mg/L and 0.21 mg/L respectively. The ratio between IP50 and ID50 was 3.3. These parameters indicated that the influence of arsenic on differentiation of rat limb bud cells was stronger than on proliferation, and arsenic belonged to a strong teratogenic agent and a specific inhibitor. This study suggested that the specific inhibitory action of arsenic on limb bud cell differentiation did not result from the cytotoxicity, but would result from the teratogenic effects of arsenic.
Keywords:limb bud cell   micromass culture   differentiation   proliferation   arsenic   teratogenicity
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