Caco-2细胞的质膜Fe(3+)-还原酶活性在分化过程中受到调节。

C Ekmekcioglu, G Strauss-Blasche, W Marktl
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引用次数: 6

摘要

本研究的目的是探讨Caco-2细胞的刷状缘膜铁还原酶活性是否在细胞分化过程中受到调节。通过测定培养时间内铁还原酶的减少量,测定细胞分化不同阶段全细胞和离体微绒毛膜中铁还原酶的活性。我们的研究结果表明,与碱性磷酸酶和蔗糖酶活性相比,铁还原酶活性在快速生长的细胞中下降,并在融合后的细胞中重新激活,而碱性磷酸酶和蔗糖酶活性在分化过程中逐渐表达,作为细胞成熟的常规指标。在增殖对数期细胞中,铁还原酶活性最低,而新鲜播种或高度分化的细胞中,铁还原酶活性显著较高。在无血清条件下生长的细胞与在标准条件下繁殖的细胞具有相似的铁还原率。通过不同途径影响细胞代谢的试剂或激素对这一跨质膜氧化还原系统无显著影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The plasma membrane Fe(3+)-reductase activity of Caco-2 cells is modulated during differentiation.

The aim of the present study was to investigate whether the brush border membrane ferric reductase activity of Caco-2 cells is modulated during cell differentiation. The ferric reductase activity was determined in whole cells and isolated microvillous membranes at different stages of cell differentiation by measuring the amount of Fe3+ reduced during the incubation time. Our results indicated that the ferric reductase activity decreased in fastly growing cells and reactivated in postconfluent cells in contrast to the alkaline phosphatase and sucrase activities which were progressively expressed during differentiation as conventional indicators of cell maturity. The lowest ferric reductase activity was found in cells at the log phase of proliferation, while freshly seeded or highly differentiated cells had significantly higher enzyme activities. Cells grown under serum-free conditions had similar ferric iron reduction rates as cells propagated under standard conditions. Reagents or hormones affecting cell metabolism through different pathways had no significant effect on this transplasma membrane redox system.

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