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Contributions of triggering-receptor-expressed-on-myeloid-cells-2 to neurological diseases

机译:触发受体表达骨髓细胞-2至神经疾病的贡献

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摘要

Recent laboratory and gene sequencing data suggest that variations in receptors called the "triggering-receptors-expressed-on-myeloid-cells" (TREMs) are implicated in Alzheimer's disease, Parkinson's disease, multiple sclerosis, and frontotemporal lobar degeneration. TREM receptors are thought to play a critical role in regulating the immune system, inflammation, and certain cellular functions. One TREM, in particular, TREM2, is highly expressed on cells of the myeloid lineage. The binding of TREM2 to the adapter protein, DNAX activating protein of 12 kD (DAP12), in microglial cells has been shown to modulate phagocytosis within the nervous system. This review highlights the role of TREM2 in neurological diseases. Moreover, here we consider potential contributions of TREM2 and mechanisms underlying TREM2 activity as contributing to neurodegeneration. These findings may provide novel insights and opportunities to consider, especially for clinicians, as they diagnose and treat certain neurological diseases.
机译:最近的实验室和基因测序数据表明,称为“触发受体表达的骨髓细胞”(TREMS)(TREMS)的受体的变化涉及阿尔茨海默病,帕金森病,多发性硬化和额定颞叶退化。据思想,TREM受体在调节免疫系统,炎症和某些细胞功能方面发挥着关键作用。特别是TEMP2,在骨髓谱系的细胞上高度表达。已经证明,在微胶质细胞中,Trem2对适配器蛋白,12kD(DAP12)的DNAX活化蛋白的结合已被证明在神经系统内调节吞噬作用。本综述突出了Trem2在神经疾病中的作用。此外,在这里,我们认为Trem2和机制潜在的Trem2活性的机制,以及促成神经变性。这些调查结果可以提供新的见解和机会,特别是对于临床医生,因为它们诊断和治疗某些神经疾病。

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