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B-hTIM4 mice
Strain Name C57BL/6-Timd4tm2(TIMD4)/Bcgen Common Name  B-hTIM4 mice
Background C57BL/6 Catalog number  110837
Aliases 
SMUCKLER, TIM4
Gene description

T-cell immunoglobulin and mucin domain containing 4 (TIMD-4) also known as T-cell membrane protein 4 (TIM-4) is a protein in humans that is encoded by the TIMD4 gene. TIM-4 genes are in mouse present on chromosome 11B1.1 and in humans on chromosome 5q33.2. TIM-4 contains IgV domain with integrin-binding site as well as a unique metal-ion-dependent ligand binding site for phosphatidylserin. TIM-4 also contains mucin domain with high levels of O-glycosylation. In comparison to other TIM proteins (such as TIM-1, TIM-2...) it does not contain tyrosin-phosphorylation motif in its intracellular tail domain.
TIM-4 is expressed on APCs such as dendritic cells or macrophages. TIM-4 serves as a ligand for TIM-1 but also as a receptor for phosphatidylserin. Its phosphatidylserin binding however does not mediate signaling instead it works more as a tethering receptor. Its phosphatidylserin binding properties also play an important role in removal of apoptotic cells. Moreover recognition of phosphatidylserin also helps to control adaptive immune system by clearing phosphatidylserin expressing apoptotic T cells. That leads to the regulation of antigen specific memory T cells. TIM-4 is also able to inhibit naive T cells by non-TIM-1 receptor binding but once T cells are active TIM-4 works as positive regulator helping to maintain their activity. TIM-4 expression on macrophages plays an important role in their homeostatic maintenance.

It was shown that TIM-4 plays a role in Th2 development. As such it plays a role in the development of allergies and might be a target for future therapies. TIM-4 was also recognized as a factor in tumor development. For example it was shown that TIM-4 promotes colorectal cancer by activating angiogenesis and recruiting tumor associated macrophages. TIM-4 also mediates autophagy at the site of tumor, which leads to reduced antigen presentation leading to increased toleration of tumor by the immune system. Therefore there are studies using the blockade of TIM-4 as a complementary therapy for cancer treatment.


mRNA expression analysis


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Strain specific analysis of TIM4 gene expression in wild-type C57BL/6 mice and B-hTIM4 mice by RT-PCR. Mouse TIM4 mRNA was detectable only in liver of wild-type C57BL/6 mice (+/+). Human TIM4 mRNA was detectable only in homozygous B-hTIM4 mice (H/H), but not in wild-type mice. 

Protein expression analysis


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Strain specific TIM4 expression analysis in homozygous B-hTIM4 mice by flow cytometry. Macrophages in peritoneal lavage fluid were collected from wild-type C57BL/6 mice (+/+) and homozygous B-hTIM4 mice (H/H), and analyzed by flow cytometry with species-specific anti-TIM4 antibody. Mouse TIM4 was detectable in wild-type C57BL/6 mice. Human TIM4 was exclusively detectable in homozygous B-hTIM4 mice but not in wild-type C57BL/6 mice.