Src-like adaptor protein regulates TCR expression on thymocytes by linking the ubiquitin ligase c-Cbl to the TCR complex

被引:0
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作者
Margaret D Myers
Tomasz Sosinowski
Leonard L Dragone
Carmen White
Hamid Band
Hua Gu
Arthur Weiss
机构
[1] Rosalind Russell Medical Research Center for Arthritis,Department of Medicine
[2] Howard Hughes Medical Institute,Division of Pediatric Immunology/Rheumatology, Department of Pediatrics
[3] University of California San Francisco,Division of Molecular Oncology, Department of Medicine
[4] Howard Hughes Medical Institute and National Jewish Medical and Research Center,Department of Biochemistry, Molecular Biology & Cell Biology and Robert H. Lurie Comprehensive Cancer Center
[5] University of California San Francisco,Microbiology Department
[6] Evanston Northwestern Healthcare Research Institute,undefined
[7] Feinberg School of Medicine,undefined
[8] Northwestern University,undefined
[9] Columbia University,undefined
[10] College of Physicians and Surgeons,undefined
来源
Nature Immunology | 2006年 / 7卷
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摘要
The adaptor molecule SLAP and E3 ubiquitin ligase c-Cbl each regulate expression of T cell receptor (TCR)–CD3 on thymocytes. Here we provide genetic and biochemical evidence that both molecules function in the same pathway. TCR-CD3 expression was similar in the absence of SLAP and/or c-Cbl. SLAP and c-Cbl were found to interact, and their expression together downregulated CD3ε. This required multiple domains in SLAP and the ring finger of c-Cbl. Furthermore, expression of SLAP and c-Cbl together induced TCRζ ubiquitination and degradation, preventing the accumulation of fully assembled recycling TCR complexes. These studies indicate that SLAP links the E3 ligase activity of c-Cbl to the TCR, allowing for stage-specific regulation of TCR expression.
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页码:57 / 66
页数:9
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