toll样受体,先天免疫系统的关键

Alaa Fadhel Hassan
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引用次数: 1

摘要

toll样受体(TLRs)是完整糖蛋白家族的成员,由细胞内和内质域组成。tlr广泛分布于机体组织中,由免疫细胞和非免疫细胞表达。它们能够识别引起细胞损伤的病原体,并将其与无害微生物区分开来,并将病原核酸作为它们的结合配体。与配体结合后,tlr首先发生构象变化;无论是形成同型二聚体还是异源二聚体,开始的信号通路都涉及适配器分子的利用,然后通过髓系差异(MyD)-88依赖或独立的途径进行信号转导。以几个转录因子(TF)的激活、促炎细胞因子(CK)和I型干扰素(IFN)的释放和炎症的开始而结束。由于潜在的疾病和紊乱,tlr参与了几乎所有的炎症过程,这使它们成为治疗开发的有趣靶点,通过合成不同的激动剂,拮抗剂,甚至是自然抗体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Toll-Like Receptors, Keys of the Innate Immune System
Toll-like receptors (TLRs) are members of the integral glycoproteins family, which are consist of intracellular and endoplasmic domains. TLRs are widely distributed in body tissues and expressed by immune and nonimmune cells. They are able to identify pathogens that cause cell injury and distinguish them from harmless microbes, and pathogenic nucleic acids as their binding ligand. Upon binding to their ligands, TLRs first underwent conformational changes; either forming homodimers or heterodimers, starting signaling pathways involve adaptor molecules utilization and then signal transduction through either myeloid differential (MyD)-88 dependent or independent pathways. Ending with activation of several transcription factors (TF) and release of pro-inflammatory cytokines (CK) and Type I interferons (IFN) and initiation of inflammation. TLRs are involved in almost all-inflammatory processes due to underlying disorders and diseases, which made them interesting targets for therapeutic development, via the synthesis of different agonists, antagonists, and even naturalized antibodies.
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