Bhattacharjee Surjyadipta, Zhao Yuhai, Dua Prerna, Rogaev Evgeny I, Lukiw Walter J
LSU Neuroscience Center, Louisiana State University Health Science Center, New Orleans, LA, 70112, United States of America.
Department of Anatomy and Cell Biology, Louisiana State University Health Science Center, New Orleans, LA, 70112, United States of America.
PLoS One. 2016 Mar 7;11(3):e0150211. doi: 10.1371/journal.pone.0150211. eCollection 2016.
The aggregation of Aβ42-peptides and the formation of drusen in age-related macular degeneration (AMD) are due in part to the inability of homeostatic phagocytic mechanisms to clear self-aggregating Aβ42-peptides from the extracellular space. The triggering receptor expressed in myeloid/microglial cells-2 (TREM2), a trans-membrane-spanning, sensor-receptor of the immune-globulin/lectin-like gene superfamily is a critical component of Aβ42-peptide clearance. Here we report a significant deficit in TREM2 in AMD retina and in cytokine- or oxidatively-stressed microglial (MG) cells. RT-PCR, miRNA-array, LED-Northern and Western blot studies indicated up-regulation of a microglial-enriched NF-кB-sensitive miRNA-34a coupled to a down-regulation of TREM2 in the same samples. Bioinformatics/transfection-luciferase reporter assays indicated that miRNA-34a targets the 299 nucleotide TREM2-mRNA-3'UTR, resulting in TREM2 down-regulation. C8B4-microglial cells challenged with Aβ42 were able to phagocytose these peptides, while miRNA-34a down-regulated both TREM2 and the ability of microglial-cells to phagocytose. Treatment of TNFα-stressed MG cells with phenyl-butyl nitrone (PBN), caffeic-acid phenethyl ester (CAPE), the NF-kB - [corrected] inhibitor/resveratrol analog CAY10512 or curcumin abrogated these responses. Incubation of anti-miRNA-34a (AM-34a) normalized miRNA-34a abundance and restored TREM2 back to homeostatic levels. These data support five novel observations: (i) that a ROS- and NF-kB - [corrected] sensitive, miRNA-34a-mediated modulation of TREM2 may in part regulate the phagocytic response; (ii) that gene products encoded on two different chromosomes (miRNA-34a at chr1q36.22 and TREM2 at chr6p21.1) orchestrate a phagocytic-Aβ42-peptide clearance-system; (iii) that this NF-kB-mediated-miRNA-34a-TREM2 mechanism is inducible from outside of the cell; (iv) that when operating normally, this pathway can clear Aβ42 peptide monomers from the extracellular medium; and (v) that anti-NF-kB and/or anti-miRNA (AM)-based therapeutic strategies may be useful against deficits in TREM-2 receptor-based-sensing and -phagocytic signaling that promote pathogenic amyloidogenesis.
在年龄相关性黄斑变性(AMD)中,Aβ42肽的聚集和玻璃膜疣的形成部分归因于稳态吞噬机制无法从细胞外空间清除自聚集的Aβ42肽。髓样/小胶质细胞-2(TREM2)中表达的触发受体是免疫球蛋白/凝集素样基因超家族的跨膜传感器受体,是Aβ42肽清除的关键组成部分。在此,我们报告了AMD视网膜以及细胞因子或氧化应激的小胶质细胞(MG)中TREM2的显著缺陷。RT-PCR、miRNA阵列、LED- Northern和蛋白质印迹研究表明同一样本中富含小胶质细胞的NF-κB敏感miRNA-34a上调,同时TREM2下调。生物信息学/转染荧光素酶报告基因检测表明miRNA-34a靶向299个核苷酸的TREM2 - mRNA - 3'UTR,导致TREM2下调。用Aβ42刺激的C8B4小胶质细胞能够吞噬这些肽,而miRNA-34a下调了TREM2以及小胶质细胞的吞噬能力。用苯基丁基硝酮(PBN)、咖啡酸苯乙酯(CAPE)、NF-κB抑制剂/白藜芦醇类似物CAY10512或姜黄素处理TNFα应激的MG细胞可消除这些反应。抗miRNA-34a(AM-34a)孵育可使miRNA-34a丰度正常化,并使TREM2恢复到稳态水平。这些数据支持五个新的观察结果:(i)ROS和NF-κB敏感的、miRNA-34a介导的TREM2调节可能部分调节吞噬反应;(ii)位于两条不同染色体上的基因产物(1号染色体q36.22处的miRNA-34a和6号染色体p21.1处的TREM2)协调一个吞噬Aβ42肽的清除系统;(iii)这种NF-κB介导的miRNA-34a - TREM2机制可从细胞外诱导;(iv)正常运作时,该途径可从细胞外介质中清除Aβ42肽单体;(v)基于抗NF-κB和/或抗miRNA(AM)的治疗策略可能对促进致病性淀粉样蛋白生成的基于TREM-2受体的传感和吞噬信号缺陷有效。