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人 MRCKα 受细胞内铁水平调节,并干扰转铁蛋白铁摄取。

Human MRCKalpha is regulated by cellular iron levels and interferes with transferrin iron uptake.

机构信息

Institute of Hematology and Blood Transfusion, Department of Cell Physiology, U Nemocnice 1, Prague 128 20, Czech Republic.

出版信息

Biochem Biophys Res Commun. 2010 Apr 30;395(2):163-7. doi: 10.1016/j.bbrc.2010.02.148. Epub 2010 Feb 25.

Abstract

Myotonic dystrophy kinase-related Cdc42-binding kinase alpha (MRCKalpha, formally known as CDC42BPA) is a serine/threonine kinase that can regulate actin/myosin assembly and activity. Recently, it has been shown that it possesses a functional iron responsive element (IRE) in the 3'-untranslated region (UTR) of its mRNA, suggesting that it may be involved in iron metabolism. Here we report that MRCKalpha protein expression is also regulated by iron levels; MRCKalpha colocalizes with transferrin (Tf)-loaded transferrin receptors (TfR), and attenuation of MRCKalpha expression by a short hairpin RNA silencing construct leads to a significant decrease in Tf-mediated iron uptake. Our results thus indicate that MRCKalpha takes part in Tf-iron uptake, probably via regulation of Tf-TfR endocytosis/endosome trafficking that is dependent on the cellular cytoskeleton. Regulation of the MRCKalpha activity by intracellular iron levels could thus represent another molecular feedback mechanism cells could use to finely tune iron uptake to actual needs.

摘要

肌萎缩性侧索硬化症相关 CDC42 结合激酶α(MRCKα,正式名称为 CDC42BPA)是一种丝氨酸/苏氨酸激酶,可调节肌动蛋白/肌球蛋白的组装和活性。最近的研究表明,其 mRNA 的 3'非翻译区(UTR)中存在一个功能性铁反应元件(IRE),提示其可能参与铁代谢。本文报道了铁水平也可调节 MRCKα 蛋白的表达;MRCKα 与转铁蛋白(Tf)负载的转铁蛋白受体(TfR)共定位,短发夹 RNA 沉默构建体减弱 MRCKα 的表达可导致 Tf 介导的铁摄取显著减少。因此,我们的结果表明,MRCKα 参与 Tf-铁摄取,可能通过 Tf-TfR 内吞作用/内体运输的调节,而该调节依赖于细胞细胞骨架。细胞内铁水平对 MRCKα 活性的调节可能代表了细胞用来精细调节铁摄取以满足实际需求的另一种分子反馈机制。

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