坏死下垂在免疫应答中的作用

Young Sik Cho
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引用次数: 2

摘要

在多细胞生物中,细胞的存活和死亡应该以一种协调的方式得到很好的调节,以促进细胞的增殖、分化和发育。脊椎动物的多种生理结果取决于细胞对感染性病原体和功能受损细胞的死亡方式。细胞死亡的生理和病理作用经常被用来描述正常和疾病状态。特别是,免疫反应可能受到宿主细胞和各种免疫相关细胞的细胞死亡模式的影响。免疫原性细胞死亡无论是意外发生还是调控发生都可能引起免疫应答。具有代表性的是,细胞凋亡和坏死下垂参与了免疫反应的稳态。迄今为止,免疫系统中的细胞凋亡已被明确定义,其作用是自我识别免疫细胞的缺失和细胞毒性杀伤。然而,越来越多的证据表明,选择性程序性细胞死亡坏死性坏死可能参与免疫监视,尽管其潜在机制尚不清楚。因此,坏死性上睑下垂或程序性坏死将被强调为免疫的调节因子。随着坏死性上睑下垂的免疫作用,揭示坏死性上睑下垂及其相关的信号通路也在本文中进行了综述。复合物II由RIP1、RIP3、FADD、pro-caspase-8组成。然后,激活的RIP3招募MLKL诱导坏死过程。基于坏死信号通路,一些化学物质已被确定为坏死蛋白的药理学抑制剂。RIP1、RIP3或MLKL可以通过化学抑制剂特异性调节。
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Roles of necroptosis in immune responses
Cell survival and cell death should be well regulated in an orchestrated way for cell proliferation, differentiation, and development in multicellular organism. A variety of physiological outcomes in vertebrate is dependent on cell death modality in response to infectious pathogens and functionally damaged cells. Physiological and pathological roles of cell death are often addressed to describe normal and disease state. Particularly, immune responses can be affected from cell death modes of host cells and various immune-associated cells. Immunogenic cell death occurs in either an accidental or a regulated way could elicit the immune responses. Representatively, apoptosis and necroptosis are involved in homeostasis of immune reaction. So far, apoptosis in immune system has been well defined, acting as deletion of self-recognizing immune cells and cytotoxic killing. However, it has been a growing body of evidence that alternative programmed cell death necroptosis could be involved in immune surveillance, although its underlying mechanism remains elusive. Therefore, necroptosis or programmed necrosis will be emphasized as a regulator of immunity. With immunological role of necroptosis, unmasking of necroptosis and its associated signaling pathway are also dealt in this review. complex II consisting of RIP1, RIP3, FADD, pro-caspase-8. Then, activated RIP3 recruits MLKL to induce the necrotic process. Based on necroptotic signaling pathway, some chemicals have been identified as pharmacological inhibitors of the necroptotic proteins. RIP1, RIP3 or MLKL can be specifically modulated by chemical inhibitors indicated.
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