Villegas-Llerena Claudio, Phillips Alexandra, Garcia-Reitboeck Pablo, Hardy John, Pocock Jennifer M
Department of Neuroinflammation, University College London, Institute of Neurology, 1 Wakefield Street, London WC1 N 1PK, UK; Department of Molecular Neuroscience, University College London, Institute of Neurology, 1 Wakefield Street, London WC1 N 1PK, UK.
Department of Neuroinflammation, University College London, Institute of Neurology, 1 Wakefield Street, London WC1 N 1PK, UK.
Curr Opin Neurobiol. 2016 Feb;36:74-81. doi: 10.1016/j.conb.2015.10.004. Epub 2015 Oct 24.
Neuroinflammation is a pathological hallmark of Alzheimer's disease (AD), and microglia, the brain's resident phagocyte, are pivotal for the immune response observed in AD. Microglia act as sentinel and protective cells, but may become inappropriately reactive in AD to drive neuropathology. Recent Genome Wide Association Studies (GWAS) have identified more than 20 gene variants associated with an increased risk of late-onset AD (LOAD), the most prevalent form of AD [1]. The findings strongly implicate genes related to the immune response (CR1, CD33, MS4A, CLU, ABCA7, EPHA1 and HLA-DRB5-HLA-DRB1), endocytosis (BIN1, PICALM, CD2AP, EPHA1 and SORL1) and lipid biology (CLU, ABCA7 and SORL1) [2-8], and many encode proteins which are highly expressed in microglia [1]. Furthermore, recent identification of a low frequency mutation in the gene encoding the triggering receptor expressed in myeloid cells 2 protein (TREM2) confers increased risk of AD in LOAD cohorts with an effect size similar to that for APOE, until recently the only identified genetic risk factor associated with LOAD [9,10(••)] (Figure 1). The present review summarises our current understanding of the probable roles of microglial genes in the regulation of neuroinflammatory processes in AD and their relation to other processes affecting the disease's progression.
神经炎症是阿尔茨海默病(AD)的一个病理标志,而小胶质细胞作为大脑中的常驻吞噬细胞,在AD中观察到的免疫反应中起关键作用。小胶质细胞作为哨兵和保护细胞,但在AD中可能会出现不适当的反应,从而推动神经病理学发展。最近的全基因组关联研究(GWAS)已经确定了20多个与晚发性AD(LOAD,AD最常见的形式)风险增加相关的基因变异[1]。这些发现强烈暗示了与免疫反应(CR1、CD33、MS4A、CLU;ABCA7、EPHA1和HLA-DRB5-HLA-DRB1)、内吞作用(BIN1、PICALM、CD2AP、EPHA1和SORL1)以及脂质生物学(CLU、ABCA7和SORL1)相关的基因[2-8],而且许多基因编码的蛋白质在小胶质细胞中高度表达[1]。此外,最近在编码髓系细胞触发受体2蛋白(TREM2)的基因中发现的一个低频突变,在LOAD队列中增加了AD的风险,其效应大小与APOE相似,APOE直到最近一直是唯一确定的与LOAD相关的遗传风险因素[9,10(••)](图1)。本综述总结了我们目前对小胶质细胞基因在AD神经炎症过程调节中的可能作用及其与影响疾病进展的其他过程之间关系的理解。