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The Regulation and Functions of activin and follistatin in Inflammation and Immunity

机译:激活素和卵泡抑素在炎症和免疫中的调节和功能

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The activins are members of the transforming growth factor (3 superfamily with broad and complex effects on cell growth and differentiation. Activin A has long been known to be a critical regulator of inflammation and immunity, and similar roles are now emerging for activin B, with which it shares 65% sequence homology. These molecules and their binding protein, follistatin, are widely expressed, and their production is increased in many acute and chronic inflammatory conditions. Synthesis and release of the activins are stimulated by inflammatory cytokines, Toll-like receptor ligands, and oxidative stress. The activins interact with heterodimeric serine/threonine kinase receptor complexes to activate SMAD transcription factors and the MAP kinase signaling pathways, which mediate inflammation, stress, and immunity. Follistatin binds to the activins with high affinity, thereby obstructing the activin receptor binding site, and targets them to cell surface proteoglycans and lysosomal degradation. Studies on transgenic mice and those with gene knockouts, together with blocking studies using exogenous follistatin, have established that activin A plays critical roles in the onset of cachexia, acute and chronic inflammatory responses such as septicemia, colitis and asthma, and fibrosis. However, activin A also directs the development of monocyte/macrophages, myeloid dendritic cells, and T cell subsets to promote type 2 and regulatory immune responses. The ability of both endogenous and exogenous follistatin to block the proinflam-matory and profibrotic actions of activin A has led to interest in this binding protein as a potential therapeutic for limiting the severity of disease and to improve subsequent damage associated with inflammation and fibrosis. However, the ability of activin A to sculpt the subsequent immune response as well means that the full range of effects that might arise from blocking activin bioactivity will need to be considered in any therapeutic ap...
机译:激活素是转化生长因子的成员(3个超家族,对细胞的生长和分化具有广泛而复杂的作用。激活素A一直是炎症和免疫的关键调节剂,现在,激活素B的相似作用正在显现。它们具有65%的序列同源性,这些分子及其结合蛋白卵泡抑素被广泛表达,并且在许多急性和慢性炎症条件下其产量都增加了,激活素的合成和释放受到炎症细胞因子Toll样受体的刺激激活素与异二聚体丝氨酸/苏氨酸激酶受体复合物相互作用,激活SMAD转录因子和MAP激酶信号传导途径,介导炎症,压力和免疫力。激活素受体结合位点,并将其靶向细胞表面蛋白聚糖和溶酶体辐射。对转基因小鼠和具有基因敲除的小鼠的研究,以及使用外源性卵泡抑素的阻断研究,已经确定,激活素A在恶病质,急性和慢性炎症反应(如败血病,结肠炎,哮喘和纤维化)的发作中起关键作用。但是,激活素A也指导单核细胞/巨噬细胞,髓样树突状细胞和T细胞亚群的发育,从而促进2型和调节性免疫反应。内源性和外源性卵泡抑素均具有阻断激活素A的促炎和纤维化作用的能力,引起了人们对该结合蛋白的兴趣,因为它是限制疾病严重程度并改善与炎症和纤维化有关的后续损害的潜在疗法。但是,激活素A雕刻随后的免疫应答的能力也意味着在任何治疗方法中都需要考虑由激活素生物活性的阻断所产生的全部作用。

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