College of Life Sciences and Bioengineering, Beijing Jiaotong University, No. 3 Shangyuan Residence, Haidian District, Beijing, 100044, China.
J Neuroinflammation. 2018 Apr 14;15(1):107. doi: 10.1186/s12974-018-1148-y.
Recent research has shown that the triggering receptor expressed on myeloid cells 2 (TREM2) in microglia is closely related to the pathogenesis of Alzheimer's disease (AD). The mechanism of this relationship, however, remains unclear. TREM2 is part of the TREM family of receptors, which are expressed primarily in myeloid cells, including monocytes, dendritic cells, and microglia. The TREM family members are cell surface glycoproteins with an immunoglobulin-like extracellular domain, a transmembrane region and a short cytoplasmic tail region. The present article reviews the following: (1) the structure, function, and variant site analysis of the Trem2 gene; (2) the metabolism of TREM2 in peripheral blood and cerebrospinal fluid; and (3) the possible underlying mechanism by which TREM2 regulates innate immunity and participates in AD.
最近的研究表明,髓系细胞触发受体 2(TREM2)在小胶质细胞中与阿尔茨海默病(AD)的发病机制密切相关。然而,这种关系的机制尚不清楚。TREM2 是 TREM 受体家族的一部分,主要表达于髓系细胞,包括单核细胞、树突状细胞和小胶质细胞。TREM 家族成员是细胞表面糖蛋白,具有免疫球蛋白样细胞外结构域、跨膜区和短胞质尾区。本文就 Trem2 基因的结构、功能及变异位点分析、外周血和脑脊液中 TREM2 的代谢、TREM2 调节固有免疫和参与 AD 的可能潜在机制进行综述。