Department of Clinical and Experimental Medicine, Medical School of Novara, Novara, Italy.
J Interferon Cytokine Res. 2011 Jan;31(1):159-72. doi: 10.1089/jir.2010.0106. Epub 2011 Jan 3.
The interferon-inducible p200 family proteins consist of a group of homologous human and mouse proteins that have an N-terminal Pyrin domain and 1 or 2 partially conserved 200 amino acid long C-terminal domains (designated the HIN domain or p200 X domain). These proteins display multifaceted activity due to their ability to bind to various target proteins (eg, transcription factors, signaling proteins, and tumor suppressor proteins) and modulate different cell functions. In addition to a role in interferon biology, increasing evidence supports a role for these proteins as regulators of various cell functions, including proliferation, differentiation, apoptosis, senescence, inflammasome assembly, and control of organ transplants. As a consequence, alterations in their expression and function may be of relevance in the pathogenesis of human diseases, such as systemic autoimmune syndromes, tumors, and degenerative diseases. This review summarizes the literature describing these data, highlights some of the important findings derived from recent studies, and speculates about future perspectives.
干扰素诱导的 p200 家族蛋白由一组同源的人类和小鼠蛋白组成,它们具有 N 端吡喃结构域和 1 或 2 个部分保守的 200 个氨基酸长的 C 端结构域(称为 HIN 结构域或 p200 X 结构域)。这些蛋白由于能够结合各种靶蛋白(例如转录因子、信号蛋白和肿瘤抑制蛋白)并调节不同的细胞功能,具有多方面的活性。除了在干扰素生物学中的作用外,越来越多的证据支持这些蛋白作为各种细胞功能的调节剂,包括增殖、分化、凋亡、衰老、炎性小体组装和器官移植的控制。因此,它们的表达和功能的改变可能与人类疾病的发病机制有关,如系统性自身免疫综合征、肿瘤和退行性疾病。本综述总结了描述这些数据的文献,强调了一些来自最近研究的重要发现,并对未来的前景进行了推测。