培养肝癌细胞的酶调节研究:胰岛素和天冬酰胺诱导鸟氨酸脱羧酶。

In Vitro Pub Date : 1984-09-01 DOI:10.1007/BF02618878
V R Potter, T R Evanson, D P Gayda, J A Gurr
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引用次数: 1

摘要

研究了胰岛素和天冬酰胺对H4-II-EC3 (H35)肝癌细胞培养中鸟氨酸脱羧酶(ODC)的诱导和降解作用。天冬酰胺的存在增强了胰岛素的反应,尽管天冬酰胺的作用与其说是对最初的增加,不如说是在补充物与新鲜培养基一起添加后6至8小时达到最大值后的下降减缓。在所有情况下,添加培养基和补充剂的初始ODC活性在零时间为零,并且在达到最大值后,活性在24小时内下降到接近零。胎牛血清的诱导过程类似,但不如胰岛素加天冬酰胺的组合,事实上,FBS抑制了后者的反应。腐胺(ODC由鸟氨酸形成的产物)在10(-5)M时,明显抑制胰岛素或FBS诱导的ODC,但当有天冬酰胺存在时,抑制作用较弱。
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Cultured hepatoma cells for the study of enzyme regulation: induction of ornithine decarboxylase by insulin and asparagine.

The induction and decay of ornithine decarboxylase (ODC) by insulin and asparagine in cultures of H4-II-EC3 (H35) hepatoma cells was studied in a modified Waymouth medium in the presence of fetal bovine serum (FBS) and in serum-free media. The insulin response was enhanced by the presence of asparagine although the effect of asparagine was not so much on the initial increase as it was on a slowing of the decline after the maximum was reached at 6 to 8 h after the supplements were added together with fresh medium. In all cases the initial ODC activity was zero at zero time for addition of media and supplements, and, after reaching the maximum, activity declined to near zero by 24 h. Fetal bovine serum gave induction that followed a similar time course but was inferior to the combination of insulin plus asparagine and, in fact, FBS inhibited the latter response. Putrescine (the product formed from ornithine by ODC), at 10(-5) M, markedly inhibited the induction of ODC by insulin or FBS, but the inhibition was less when asparagine was present.

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