共 50 条
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
相关论文