The Protein Synthesis Inhibitor Blasticidin S Enters Mammalian Cells via Leucine-rich Repeat-containing Protein 8D

被引:69
|
作者
Lee, Clarissa C. [1 ,2 ]
Freinkman, Elizaveta [1 ]
Sabatini, David M. [1 ,2 ,3 ,4 ,5 ]
Ploegh, Hidde L. [1 ,2 ]
机构
[1] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[2] MIT, Dept Biol, Cambridge, MA 02139 USA
[3] MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[4] Broad Inst, Cambridge, MA 02142 USA
[5] MIT, Howard Hughes Med Inst, Cambridge, MA 02139 USA
关键词
DOMAIN; APOPTOSIS; RELEASE;
D O I
10.1074/jbc.M114.571257
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Leucine-rich repeat-containing 8 (LRRC8) proteins have been identified as putative receptors involved in lymphocyte development and adipocyte differentiation. They remain poorly characterized, and no specific function has been assigned to them. There is no consensus on how this family of proteins might function because homology searches suggest that members of the LRRC8 family act not as plasma membrane receptors, but rather as channels that mediate cell-cell signaling. Here we provide experimental evidence that supports a role for LRRC8s in the transport of small molecules. We show that LRRC8D is a mammalian protein required for the import of the antibiotic blasticidin S. We characterize localization and topology of LRRC8A and LRRC8D and demonstrate that LRRC8D interacts with LRRC8A, LRRC8B, and LRRC8C. Given the suggested involvement in solute transport, our results support a model in which LRRC8s form one or more complexes that may mediate cell-cell communication by transporting small solutes.
引用
收藏
页码:17124 / 17131
页数:8
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