| Literature DB >> 18367551 |
Masayuki Mizui1, Takashi Shikina, Hisashi Arase, Kazuhiro Suzuki, Teruhito Yasui, Paul D Rennert, Atsushi Kumanogoh, Hitoshi Kikutani.
Abstract
T cell Ig and mucin domain (TIM)-4 is preferentially expressed on antigen-presenting cells, and its counter-ligand, TIM-1, is thought to deliver co-stimulating signals to T cells. However, the physiological functions of TIM-4 remain unclear. Here, we demonstrate that TIM-4 inhibits naive T cell activation through a ligand other than TIM-1. The inhibitory effect of TIM-4 was specific to naive T cells which do not express TIM-1, and the effect disappeared in pre-activated T cells. Conversely, antibody-mediated blockade of TIM-4 in vivo substantially suppressed T cell-mediated inflammatory responses despite enhanced generation of antigen-specific T cells. Furthermore, treatment with anti-TIM-4 reduced the inflammatory responses developed in mice that were adoptively transferred with antigen-primed T cells. These results suggest that TIM-4 exerts bimodal functions depending on the activation status of T cells.Entities:
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Year: 2008 PMID: 18367551 DOI: 10.1093/intimm/dxn029
Source DB: PubMed Journal: Int Immunol ISSN: 0953-8178 Impact factor: 4.823