TPA对培养的小鼠Y-1肾上腺皮质肿瘤细胞形态学、生长和类固醇效应的表征。

S A Murray, S Polizotto
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引用次数: 4

摘要

促瘤剂12-0-十四烷醇-13-醋酸酯(TPA)引起Y-1肾上腺皮质肿瘤细胞的时间和剂量依赖性形态学改变。在细胞培养中加入1微克/毫升TPA 2小时后,形态学改变明显,随着处理时间的延长,形态学改变更加明显。小剂量的TPA需要更长的时间才能产生效果。在有TPA的培养基中培养的细胞比在没有TPA的培养基中培养的细胞表现出更多的圆角和堆积。这些tpa刺激的形态学变化是可逆的,在不含tpa的培养基中培养24小时后,培养的细胞开始变平。在不含tpa的培养基中培养96小时后,它们与对照培养相似。形态学改变的可逆性也具有剂量依赖性:1微克/毫升TPA处理的细胞恢复典型对照形态所需的时间比0.01微克/毫升TPA处理的细胞要长。此外,TPA处理导致细胞生长速度下降,类固醇产生增加,细胞质中camp依赖性蛋白激酶的游离催化单元定位增加。在TPA中维持的培养中,ACTH对细胞群的类固醇生成作用被抑制。本研究结果表明,TPA可诱导Y-1肾上腺皮质肿瘤细胞群的形态学改变,增加甾体生成和camp依赖性蛋白激酶的激活,降低细胞生长速率。
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Characterization of the morphological, growth, and steroidogenic effect of TPA on mouse Y-1 adrenal cortical tumor cells in culture.

The tumor-promoting agent 12-0-tetradecanoyl-phorbol-13-acetate (TPA) caused a time- and dose-dependent morphological change in Y-1 adrenocortical tumor cells. The morphological alteration was apparent 2 hr following addition of 1 microgram/ml TPA to cell cultures and became more striking with longer treatment times. Smaller doses of TPA took a longer time to produce an effect. Cultures grown in the presence of TPA exhibited more rounding and piling up of cells than similar cultures maintained in medium lacking TPA. These TPA-stimulated morphological changes were reversible, and after 24 hr in TPA-free media, the cultured cells began to flatten. After 96 hr in TPA-free media they resembled the control cultures. The reversibility of the morphological change was also dose dependent: cells treated with 1 microgram/ml TPA took a longer time to resume the typical control morphology than did cultures treated with 0.01 microgram/ml TPA. In addition, TPA treatment resulted in a decrease in cell growth rate, an increase in steroid production, and an increase in the localization of free catalytic units of cAMP-dependent protein kinase in the cytoplasm. The steroidogenic effect of ACTH on the cell population was inhibited in cultures maintained in TPA. The results of this study indicate that TPA induces morphological changes in the Y-1 adrenocortical tumor cell population while increasing steroidogenesis and the activation of cAMP-dependent protein kinase and decreasing cell growth rate.

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