Ekmekcioglu C, Strauss-Blasche G, Marktl W
Department of Medical Physiology, University of Vienna, Medical School, Austria.
Biochem Mol Biol Int. 1998 Dec;46(5):951-61. doi: 10.1080/15216549800204502.
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.
本研究的目的是调查在细胞分化过程中,Caco-2细胞刷状缘膜铁还原酶活性是否受到调节。通过测量孵育期间Fe3+的还原量,在细胞分化的不同阶段对全细胞和分离的微绒毛膜中的铁还原酶活性进行了测定。我们的结果表明,与碱性磷酸酶和蔗糖酶活性不同,铁还原酶活性在快速生长的细胞中降低,而在汇合后的细胞中重新激活,碱性磷酸酶和蔗糖酶活性在分化过程中作为细胞成熟的传统指标逐渐表达。在增殖对数期的细胞中发现铁还原酶活性最低,而新接种的或高度分化的细胞具有明显更高的酶活性。在无血清条件下生长的细胞与在标准条件下增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种跨质膜氧化还原系统没有显著影响。