Zhao Hua, Gonzalezgugel Elena, Cheng Lei, Richbourgh Brendon, Nie Lin, Liu Chuanju
Department of Orthopaedic Surgery, New York University School of Medicine, New York, NY 10003, United States ; Department of Spine Surgery, Qilu Hospital of Shandong University, Jinan, 250014, China.
Department of Orthopaedic Surgery, New York University School of Medicine, New York, NY 10003, United States.
Genes Dis. 2015 Mar;2(1):46-56. doi: 10.1016/j.gendis.2014.10.003.
p204 is a member of the interferon-inducible p200 family proteins in mice. The p200 family has been reported to be multifunctional regulators of cell proliferation, differentiation, apoptosis and senescence. Interferon-inducible protein 16 (IFI16) is regarded as the human ortholog of p204 in several studies. This is possibly due to the similarity of their structures. However the consistency of their functions is still elusive. Currently, an emerging focus has been placed upon the role of the p200 proteins as sensors for microbial DNA in innate immune responses and provides new insights into infections as well as autoimmune diseases. This review specially focuses on IFI16 and p204, the member of p200 family in human and murine respectively, and their pathophysiological roles in innate immune responses, cell differentiation and proliferation.
p204是小鼠中干扰素诱导的p200家族蛋白的成员。据报道,p200家族是细胞增殖、分化、凋亡和衰老的多功能调节因子。在多项研究中,干扰素诱导蛋白16(IFI16)被认为是p204在人类中的同源物。这可能是由于它们结构的相似性。然而,它们功能的一致性仍然难以捉摸。目前,人们越来越关注p200蛋白在先天免疫反应中作为微生物DNA传感器的作用,并为感染以及自身免疫性疾病提供了新的见解。本综述特别关注IFI16和p204,它们分别是人类和小鼠p200家族的成员,以及它们在先天免疫反应、细胞分化和增殖中的病理生理作用。