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人胎盘绒毛在器官培养中的生存能力。

Viability of the human placental villi in organ culture.

作者信息

Ogino M, Satoh M, Kinoshita K, Satoh K, Mizuno M, Sakamoto S

出版信息

Arch Gynecol. 1984;234(4):235-46. doi: 10.1007/BF02113808.

Abstract

The viability of the placental villi in organ culture was investigated both from the morphological and functional points of view. Morphological viability was judged on the appearance of the villi with special emphasis on the trophoblastic cells and the morphological integrity of the placental villi could be maintained for at least 96 h in organ culture. Functional viability was judged by analyses of delta 5-3 beta-hydroxysteroid dehydrogenase; delta 5,4-isomerase (3 beta-HSD) activity with 14C-pregnenolone as the substrate and by the suppressive effect of the cultivated villi on the secretion of plasminogen activator (PA) obtained from mouse peritoneal macrophages stimulated by OK-432. It was found that the 3 beta-HSD activity and suppressive effect on PA secretion could be preserved for at least 120 h in organ culture.

摘要

从形态学和功能学角度对胎盘绒毛在器官培养中的活力进行了研究。形态学活力根据绒毛的外观判断,特别强调滋养层细胞,并且胎盘绒毛的形态完整性在器官培养中可维持至少96小时。功能活力通过以14C-孕烯醇酮为底物分析δ5-3β-羟基类固醇脱氢酶;δ5,4-异构酶(3β-HSD)活性,以及通过培养的绒毛对由OK-432刺激的小鼠腹腔巨噬细胞分泌的纤溶酶原激活剂(PA)的抑制作用来判断。结果发现,在器官培养中,3β-HSD活性和对PA分泌的抑制作用可维持至少120小时。

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