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分子复合物 TREM-2/DAP12 的结构、表达模式和生物学活性。

Structure, expression pattern and biological activity of molecular complex TREM-2/DAP12.

机构信息

Department of Biochemistry and Molecular Biology, Institute of Rheumatology, Warsaw, Poland.

出版信息

Hum Immunol. 2013 Jun;74(6):730-7. doi: 10.1016/j.humimm.2013.02.003. Epub 2013 Feb 28.

Abstract

DNAX-activating protein of 12kDa (DAP12) is a member of type I transmembrane adapter proteins containing immunoreceptor tyrosine-based activation motifs (ITAMs). In humans DAP12 gene is located on chromosome 19q13.1. DAP12 forms a molecular complex with triggering receptor expressed on myeloid cells two (TREM-2). TREM-2 ligation leads to the activation of Src family kinases, phosphorylation of tyrosine residues in the ITAM of DAP12, recruitment of the Syk and ZAP70 tyrosine kinases and initiation of an intracellular signaling cascade. Depending on the cell type, DAP12/TREM-2 activation plays an important role in activation and differentiation of osteoclasts, phagocytosis of bacteria, brain and bone homeostasis and inhibition of the toll-like receptor (TLR) signaling in macrophages and dendritic cells. A proper understanding of the function of this complex receptor has been restrained because of the elusive nature of TREM-2 ligands. Here we review the structure, biological functions and signaling pathways of DAP12 and its associated receptor TREM-2.

摘要

12kDa 的 DNAX 激活蛋白 (DAP12) 是一种含有免疫受体酪氨酸激活基序 (ITAM) 的 I 型跨膜衔接蛋白家族成员。在人类中,DAP12 基因位于 19q13.1 染色体上。DAP12 与髓样细胞表达的触发受体 2(TREM-2)形成一个分子复合物。TREM-2 的配体结合导致Src 家族激酶的激活,DAP12 的 ITAM 中的酪氨酸残基磷酸化,Syk 和 ZAP70 酪氨酸激酶的募集以及细胞内信号级联的启动。根据细胞类型的不同,DAP12/TREM-2 的激活在破骨细胞的激活和分化、细菌的吞噬作用、脑和骨的稳态以及巨噬细胞和树突状细胞中 Toll 样受体 (TLR) 信号的抑制中发挥重要作用。由于 TREM-2 配体难以捉摸,因此对该复杂受体功能的正确理解受到限制。本文综述了 DAP12 及其相关受体 TREM-2 的结构、生物学功能和信号通路。

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