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人类 TRPV5 和 TRPV6:镉和锌毒性的关键参与者。

Human TRPV5 and TRPV6: key players in cadmium and zinc toxicity.

机构信息

Institute of Biochemistry and Molecular Medicine, University of Bern, 3012 Bern, Switzerland; Swiss National Centre of Competence in Research, NCCR TransCure, University of Bern, Switzerland.

出版信息

Cell Calcium. 2013 Oct;54(4):276-86. doi: 10.1016/j.ceca.2013.07.003. Epub 2013 Aug 20.

Abstract

TRPV5 and TRPV6 are two major calcium transport pathways in the human body maintaining calcium homeostasis. TRPV5 is mainly expressed in the distal convoluted and connecting tubule where it is the major, regulated pathway for calcium reabsorption. TRPV6 serves as an important calcium entry pathway in the duodenum and the placenta. Previously, we showed that human TRPV6 (hTRPV6) transports several heavy metals. In this study we tested whether human TRPV5 (hTRPV5) also transports cadmium and zinc, and whether hTRPV5 together with hTRPV6 are involved in cadmium and zinc toxicity. The hTRPV5 mRNA and protein were expressed in HEK293 cells transiently transfected with pTagRFP-C1-hTRPV5. The overexpression of the hTRPV5 protein at the plasma membrane was revealed by cell surface biotinylation and immunofluorescence techniques. We observed that both cadmium and zinc permeate hTRPV5 in ion imaging experiments using Fura-2 or Newport Green DCF. Our results were further confirmed using whole-cell patch clamp technique. Transient overexpression of hTRPV5 or hTRPV6 sensitized cells to cadmium and zinc. Toxicity curves of cadmium and zinc were also shifted in hTRPV6 expressing HEK293 cells clones. Our results suggest that TRPV5 and TRPV6 are crucial gates controlling cadmium and zinc levels in the human body especially under low calcium dietary conditions, when these channels are maximally upregulated.

摘要

TRPV5 和 TRPV6 是人体中维持钙稳态的两种主要钙转运途径。TRPV5 主要表达在远曲小管的连接段,是钙重吸收的主要调节途径。TRPV6 作为十二指肠和胎盘的重要钙内流途径。先前,我们表明人类 TRPV6(hTRPV6)转运多种重金属。在这项研究中,我们测试了 hTRPV5 是否也转运镉和锌,以及 hTRPV5 是否与 hTRPV6 一起参与镉和锌的毒性。用 pTagRFP-C1-hTRPV5 瞬时转染 HEK293 细胞表达 hTRPV5 mRNA 和蛋白。通过细胞表面生物素化和免疫荧光技术揭示 hTRPV5 蛋白在质膜上的过表达。我们观察到在使用 Fura-2 或 Newport Green DCF 的离子成像实验中,镉和锌均透过 hTRPV5。我们的结果使用全细胞膜片钳技术进一步得到证实。hTRPV5 或 hTRPV6 的瞬时过表达使细胞对镉和锌敏感。镉和锌的毒性曲线在表达 hTRPV6 的 HEK293 细胞克隆中也发生了转移。我们的结果表明,TRPV5 和 TRPV6 是控制人体中镉和锌水平的关键门户,尤其是在低钙饮食条件下,这些通道被最大程度地上调时。

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