Fyn binds to and phosphorylates T cell immunoglobulin and mucin domain-1 (Tim-1)

被引:17
|
作者
Curtiss, Miranda L. [1 ,2 ,3 ]
Hostager, Bruce S. [1 ]
Stepniak, Elizabeth [1 ]
Singh, Melody [1 ]
Manhica, Natalie [1 ]
Knisz, Judit [1 ]
Traver, Geri [1 ]
Rennert, Paul D. [4 ]
Colgan, John D. [1 ]
Rothman, Paul B. [1 ]
机构
[1] Univ Iowa, Dept Internal Med, Carver Coll Med, Iowa City, IA 52242 USA
[2] Univ Iowa, Med Scientist Training Program, Carver Coll Med, Iowa City, IA 52242 USA
[3] Univ Iowa, Interdisciplinary Grad Program Immunol, Carver Coll Med, Iowa City, IA 52242 USA
[4] Biogen Idec Inc, Cambridge, MA 01746 USA
关键词
Tim-1; Havcr-1; B cell; Fyn; Signaling; MONKEY KIDNEY-CELLS; HEPATITIS-A VIRUS; IG-ALPHA; PHOSPHATIDYLSERINE RECEPTOR; HUMORAL IMMUNITY; APOPTOTIC CELLS; B-CELLS; ACTIVATION; FAMILY; IDENTIFICATION;
D O I
10.1016/j.molimm.2011.03.023
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
The gene encoding T cell immunoglobulin and mucin domain-1 (Tim-1) is linked to atopy and asthma susceptibility in mice and humans. Tim-1 is a transmembrane protein expressed on activated lymphocytes and appears to have a role as a co-stimulatory receptor in T cells. The protein has not been shown to have enzymatic activity but contains a site within its cytoplasmic tail predicted to be a target for tyrosine kinases. Here, we show that Tim-1 can associate with the kinase Fyn, a member of the Src family of tyrosine kinases. This association does not require Fyn's kinase activity and is independent of the phosphorylation of a conserved tyrosine present within the cytoplasmic tail of Tim-1. Fyn is necessary for phosphorylation of this tyrosine in Tim-1 and the phosphorylation of Tim-1 varies with the levels of Fyn present in cells. These data suggest a role for Fyn in the signaling downstream of Tim-1. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1424 / 1431
页数:8
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