Department of Diagnostic Sciences, Tufts University School of Dental Medicine, 136 Harrison Avenue, South Cove, Room 116, Boston, MA, 02111, USA; Division of Biochemistry, Department of Oral Biology and Tissue Engineering, Meikai University School of Dentistry, 1-1 Keyakidai, Sakado, Saitama, 350-0283, Japan.
Department of Diagnostic Sciences, Tufts University School of Dental Medicine, 136 Harrison Avenue, South Cove, Room 116, Boston, MA, 02111, USA.
Biochem Biophys Res Commun. 2022 Dec 20;635:227-235. doi: 10.1016/j.bbrc.2022.10.048. Epub 2022 Oct 18.
TREM2 (Triggering receptor expressed on myeloid cells 2) is the causative gene for Nasu-Hakola disease, which is characterized by multiple bone cysts and leukoencephalopathy. In addition, mutations in this gene have been found to be correlated with the onset of Alzheimer's disease. TREM2 is an immunoreceptor expressed on dendritic cells, microglia, osteoclasts, and macrophages. TREM2 on the cell membrane is shed by some proteases and released as soluble TREM2 (sTREM2). Meanwhile, several TREM2 ligands have been reported, and lipopolysaccharide (LPS) is one of the candidates. Using RNA interference to examine TREM2-mediated LPS response in macrophages, we identified five chemokines whose expression was induced via TREM2. Furthermore, we showed that LPS-induced expression of CXC-motif chemokine ligand (Cxcl10) and Cxcl11 among the five chemokines was mediated in part through sTREM2. These results suggest that sTREM2 has cytokine-like functions in macrophages.
TREM2(髓系细胞触发受体 2)是 Nasu-Hakola 病的致病基因,其特征是多发性骨囊肿和脑白质病。此外,该基因的突变已被发现与阿尔茨海默病的发病有关。TREM2 是一种表达在树突状细胞、小胶质细胞、破骨细胞和巨噬细胞上的免疫受体。细胞膜上的 TREM2 被一些蛋白酶切割并释放为可溶性 TREM2(sTREM2)。同时,已经报道了几种 TREM2 配体,其中脂多糖(LPS)是候选配体之一。使用 RNA 干扰技术在巨噬细胞中检测 TREM2 介导的 LPS 反应,我们鉴定出五种趋化因子,它们的表达被 TREM2 诱导。此外,我们表明,在这五种趋化因子中,LPS 诱导的 CXC 基序趋化因子配体(Cxcl10)和 Cxcl11 的表达部分通过 sTREM2 介导。这些结果表明 sTREM2 在巨噬细胞中具有细胞因子样功能。