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Inflammasome signalling in brain function and neurodegenerative disease

机译:脑功能和神经变性疾病中的炎症信号传导

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The mammalian CNS is an intricate and fragile structure, which on one hand is open to change in order to store information, but on the other hand is vulnerable to damage from injury, pathogen invasion or neurodegeneration. During senescence and neurodegeneration, activation of the innate immune system can occur. Inflammasomes are signalling complexes that regulate cells of the immune system, which in the brain mainly includes microglial cells. In microglia, the NLRP3 (NOD-, LRR- and pyrin domain-containing 3) inflammasome becomes activated when these cells sense proteins such as misfolded or aggregated amyloid-beta, alpha-synuclein and prion protein or superoxide dismutase, ATP and members of the complement pathway. Several other inflammasomes have been described in microglia and the other cells of the brain, including astrocytes and neurons, where their activation and subsequent caspase 1 cleavage contribute to disease development and progression.
机译:哺乳动物CNS是一种复杂和脆弱的结构,一方面是打开的,以便更改以存储信息,但另一方面易于受损损伤,病原体侵袭或神经变性。 在衰老和神经变性期间,可能发生先天免疫系统的激活。 炎症是信号配合物,其调节免疫系统的细胞,其在大脑中主要包括小胶质细胞。 当这些细胞感测蛋白如错折叠或聚集的淀粉样蛋白蛋白质或超氧化物歧化酶,ATP和成员时,在微胶质细胞中,当这些细胞感应蛋白质如错粘接或聚集的淀粉样蛋白或超氧化物歧化酶,ATP和成员时,NLRP3(NOD-,LRR-和吡啶结构域3)炎炎炎症被激活 补体途径。 在微胶质细胞和大脑的其他细胞中描述了几种其他炎性炎症,包括星形胶质细胞和神经元,其中它们的活化和随后的胱天蛋白酶1切割有助于疾病发展和进展。

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