Cleavage of TRPM7 Releases the Kinase Domain from the Ion Channel and Regulates Its Participation in Fas-Induced Apoptosis

详细信息	查看全文 | 推荐本文 |

• 作者：Bimal  ; N. Desai¹ ; ⁴ ; ⁵ ; Grigory Krapivinsky¹ ; ⁴ ; Betsy Navarro¹ ; Luba Krapivinsky¹ ; Brett  ; C. Carter² ; Sebastien Febvay² ; Markus Delling¹ ; Anirudh Penumaka¹ ; I.  ; Scott Ramsey³ ; Yunona Manasian¹ ; David  ; E. Clapham¹ ; ² ; ^{dclapham@enders.tch.harvard.edu}
• 刊名：Developmental Cell
• 出版年：2012
• 期刊代码：10_15345807
• 类别：bio
• 出版时间：12 June, 2012
• 卷：22
• 期：6
• 页码：1149-1162
• 文件大小：2105 K

摘要

| Figures/TablesFigures/Tables | ReferencesReferencession="1.0" encoding="UTF-8"?>

Summary

Transient receptor potential melastatin-like 7 (TRPM7) is a channel protein that also contains a regulatory serine-threonine kinase domain. Here, we find that Trpm7^{鈭?鈭?/sup> T聽cells are deficient in Fas-receptor-induced apoptosis and that TRPM7 channel activity participates in the apoptotic process and is regulated by caspase-dependent cleavage. This function of TRPM7 is dependent on its function as a channel, but not as a kinase. TRPM7 is cleaved by caspases at D1510, disassociating the carboxy-terminal kinase domain from the pore without disrupting the phosphotransferase activity of the released kinase but substantially increasing TRPM7 ion channel activity. Furthermore, we show that TRPM7 regulates endocytic compartmentalization of the Fas receptor after receptor stimulation, an important process for apoptotic signaling through Fas receptors. These findings raise the possibility that other members of the TRP channel superfamily are also regulated by caspase-mediated cleavage, with wide-ranging implications for cell death and differentiation.}