The Protein Synthesis Inhibitor Blasticidin S Enters Mammalian Cells via Leucine-rich Repeat-containing Protein 8D
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作者:
Lee, Clarissa C.
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Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
MIT, Dept Biol, Cambridge, MA 02139 USAWhitehead Inst Biomed Res, Cambridge, MA 02142 USA
Lee, Clarissa C.
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Freinkman, Elizaveta
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Whitehead Inst Biomed Res, Cambridge, MA 02142 USAWhitehead Inst Biomed Res, Cambridge, MA 02142 USA
Freinkman, Elizaveta
[1
]
Sabatini, David M.
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Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
MIT, Dept Biol, Cambridge, MA 02139 USA
MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
Broad Inst, Cambridge, MA 02142 USA
MIT, Howard Hughes Med Inst, Cambridge, MA 02139 USAWhitehead Inst Biomed Res, Cambridge, MA 02142 USA
Sabatini, David M.
[1
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,5
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Ploegh, Hidde L.
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Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
MIT, Dept Biol, Cambridge, MA 02139 USAWhitehead Inst Biomed Res, Cambridge, MA 02142 USA
Ploegh, Hidde L.
[1
,2
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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
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.
机构:
Cent South Univ, Xiangya Hosp, Dept Rheumatol & Immunol, Changsha, Hunan, Peoples R China
Cent South Univ, Xiangya Hosp, Natl Clin Res Ctr Geriatr Disorders, Changsha, Hunan, Peoples R ChinaCent South Univ, Xiangya Hosp, Dept Rheumatol & Immunol, Changsha, Hunan, Peoples R China
Zhu, Honglin
Meng, Meng
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Cent South Univ, Xiangya Hosp, Dept Pathol, Changsha, Hunan, Peoples R ChinaCent South Univ, Xiangya Hosp, Dept Rheumatol & Immunol, Changsha, Hunan, Peoples R China
Meng, Meng
Luo, Hui
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Cent South Univ, Xiangya Hosp, Dept Rheumatol & Immunol, Changsha, Hunan, Peoples R China
Cent South Univ, Xiangya Hosp, Natl Clin Res Ctr Geriatr Disorders, Changsha, Hunan, Peoples R ChinaCent South Univ, Xiangya Hosp, Dept Rheumatol & Immunol, Changsha, Hunan, Peoples R China
Luo, Hui
Distler, Joerg H. W.
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机构:
Heinrich Heine Univ, Univ Hosp Dusseldorf, Dept Rheumatol, Med Fac, Dusseldorf, Germany
Heinrich Heine Univ, Univ Hosp Dusseldorf, Med Fac, Hiller Res Ctr, Dusseldorf, GermanyCent South Univ, Xiangya Hosp, Dept Rheumatol & Immunol, Changsha, Hunan, Peoples R China