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双铁转铁蛋白还原刺激HeLa细胞的Na+/H+逆向转运。

Diferric transferrin reduction stimulates the Na+/H+ antiport of HeLa cells.

作者信息

Sun I L, Garcia-Cañero R, Liu W, Toole-Simms W, Crane F L, Morré D J, Löw H

出版信息

Biochem Biophys Res Commun. 1987 May 29;145(1):467-73. doi: 10.1016/0006-291x(87)91344-1.

Abstract

Proton release from HeLa cells is stimulated by external oxidants for the transplasmalemma electron transport enzymes. These oxidants, such as ferricyanide and diferric transferrin, also stimulate cell growth. We now present evidence that proton release associated with the reduction of ferricyanide and diferric transferrin is through the Na+/H+ antiport. The stoichiometry of H+/e- release with diferric transferrin is over 50 to 1, which is greater than expected for oxidation of a protonated transmembrane electron carrier. Diferric transferrin induced proton release depends on external sodium and is inhibited by amiloride. Proton release is also inhibited when diferric transferrin reduction is inhibited by apotransferrin. A tightly coupled association between the redox system and the antiport is shown by sodium dependence and amiloride inhibition of diferric transferrin reduction. The results indicate a new role for ferric transferrin in growth stimulation by activation of the sodium-proton antiport.

摘要

来自HeLa细胞的质子释放受到用于跨质膜电子传递酶的外部氧化剂的刺激。这些氧化剂,如铁氰化物和二价铁转铁蛋白,也刺激细胞生长。我们现在提供证据表明,与铁氰化物和二价铁转铁蛋白还原相关的质子释放是通过Na+/H+反向转运体进行的。二价铁转铁蛋白释放H+/e-的化学计量比超过50比1,这比质子化跨膜电子载体氧化的预期值要高。二价铁转铁蛋白诱导的质子释放依赖于外部钠,并被氨氯吡咪抑制。当脱铁转铁蛋白抑制二价铁转铁蛋白还原时,质子释放也受到抑制。钠依赖性和氨氯吡咪对二价铁转铁蛋白还原的抑制表明氧化还原系统与反向转运体之间存在紧密耦合的关联。结果表明,铁转铁蛋白通过激活钠-质子反向转运体在生长刺激中具有新的作用。

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