Peschon J J, Torrance D S, Stocking K L, Glaccum M B, Otten C, Willis C R, Charrier K, Morrissey P J, Ware C B, Mohler K M
Department of Molecular Immunology, Immunex Corp., Seattle, WA 98101, USA.
J Immunol. 1998 Jan 15;160(2):943-52.
The pleiotropic activities of the potent proinflammatory cytokine TNF are mediated by two structurally related, but functionally distinct, receptors, p55 and p75, that are coexpressed on most cell types. The majority of biologic responses classically attributed to TNF are mediated by p55. In contrast, p75 has been proposed to function as both a TNF antagonist by neutralizing TNF and as a TNF agonist by facilitating the interaction between TNF and p55 at the cell surface. We have examined the roles of p55 and p75 in mediating and modulating the activity of TNF in vivo by generating and examining mice genetically deficient in these receptors. Selective deficits in several host defense and inflammatory responses are observed in mice lacking p55 or both p55 and p75, but not in mice lacking p75. In these models, the activity of p55 is not impaired by the absence of p75, arguing against a physiologic role for p75 as an essential element of p55-mediated signaling. In contrast, exacerbated pulmonary inflammation and dramatically increased endotoxin induced serum TNF levels in mice lacking p75 suggest a dominant role for p75 in suppressing TNF-mediated inflammatory responses. In summary, these data help clarify the biologic roles of p55 and p75 in mediating and modulating the biologic activity of TNF and provide genetic evidence for an antagonistic role of p75 in vivo.
强效促炎细胞因子肿瘤坏死因子(TNF)的多效性活动是由两种结构相关但功能不同的受体介导的,即p55和p75,它们在大多数细胞类型上共同表达。传统上归因于TNF的大多数生物学反应是由p55介导的。相比之下,有人提出p75既可以通过中和TNF作为TNF拮抗剂发挥作用,也可以通过促进TNF与细胞表面p55之间的相互作用作为TNF激动剂发挥作用。我们通过培育和研究缺乏这些受体的基因缺陷小鼠,研究了p55和p75在体内介导和调节TNF活性中的作用。在缺乏p55或同时缺乏p55和p75的小鼠中观察到几种宿主防御和炎症反应的选择性缺陷,但在缺乏p75的小鼠中未观察到。在这些模型中,p75的缺失不会损害p55的活性,这表明p75作为p55介导信号传导的必需元件没有生理作用。相比之下,缺乏p75的小鼠肺部炎症加剧,内毒素诱导的血清TNF水平显著升高,这表明p75在抑制TNF介导的炎症反应中起主导作用。总之,这些数据有助于阐明p55和p75在介导和调节TNF生物学活性中的生物学作用,并为p75在体内的拮抗作用提供遗传学证据。