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作 者:陈浩宏[1,2,3] 顾芝萍[1,2,3] 游根娣 庄临之
机构地区:[1]上海基础医学院药理教研室 [2]中国科学院上海药物研究所 [3]中国科学院动物研究所生殖生物学开放研究实验室
出 处:《上海铁道大学学报》1998年第11期1-3,共3页
基 金:中国科学院动物研究所生殖生物学国家重点实验室基金
摘 要:目的建立分散的人蜕膜质细胞培养模型以用于抗生育药物的筛选研究。方法早孕6~9周的正常人蜕膜组织经胶原酶(150u/ml)和透明质酸酶(50u/ml))于35℃恒温水浴中振荡消化100min,并经216μm不锈钢网过滤后得到分离的人蜕膜基质细胞;该细胞培养于无血清培养液(以下简称培液)中,通过变换培液中添加生长因子及抗生育药物的浓度观察其生长变化情形。结果人蜕膜细胞在无血清FD+8F培液中,可维持贴壁生长3周以上。上皮生长因子、胰岛素、转铁蛋白、硒、氢化可的松及小剂量的孕酮(10-8mol/L)和雌二醇(10-8mol/L)有维持蜕膜细胞生长的作用;抗生育物质芫花酯甲(0.5μg/ml)、米非司酮(Ru486,10μg/ml)、他莫西芬(10μg/ml)、土槿皮乙酸(50μg/ml)和双炔失碳酯(60μg/ml)对于培养的人蜕膜细胞均有杀伤作用,而天花粉(100μg/ml)无明显作用。米非司酮与他莫西芬、双炔失碳酯分别合并使用,对蜕膜细胞的损伤有协同作用。结论人蜕膜细胞培养作为抗生育药物初筛模型有较多优点,有待进一步发展推广。Objective To establish an in vitro model of human decidual cell culture for screening drugs and studying antifertility drugs.Methods Normal decidual tissues at 6th 9th weeks of gestation were minced and digested for 100 min with coll. (150u/ml) and hyalu. (50u/ml) at 35℃ constantly. The resulting supernatant was filtered through the stainless steel sieve of 216 μm to obtain isolated decidual cells. The decidual cells were cultured in serum free medium. The growth and change of the cells were observed as concentrations of added growth factors or drugs were being changed.Results Human decidual cells which were cultured in serum free FD+8F medium could be kept alive for over 3 weeks. EGF, INS, TF, Se, Hydroc and low dose (10 -8 mol/L) of P and E 2 could maintain the growth of decidual cells. The results showed that Yuanhuacine (0.5μg/ml), Ru486(10μg/ml), Tamoxifen (10μg/ml), Pseudolaric acid B (50μg/ml) and Anordrin (60μg/ml) were detrimental to the decidual cells but Trichosanthin had no evident effects. Coordinative effects were observed when Ru486 was given together with Tamoxifen or Anordrin respectively.Conclusion Human decidual cell culture has more advantages as a model for screening antifertility drugs but it deserves further research to develop.
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