Hibbs Margaret L, Raftery April L, Tsantikos Evelyn
a Department of Immunology and Pathology , Alfred Medical Research and Education Precinct Monash University , Melbourne , Victoria , Australia.
Growth Factors. 2018 Dec;36(5-6):213-231. doi: 10.1080/08977194.2019.1569649. Epub 2019 Feb 15.
SHIP-1 is a hematopoietic-specific inositol phosphatase activated downstream of a multitude of receptors including those for growth factors, cytokines, antigen, immunoglobulin and toll-like receptor agonists where it exerts inhibitory control. While it is constitutively expressed in all immune cells, SHIP-1 expression is negatively regulated by the inflammatory and oncogenic micro-RNA miR-155. Knockout mouse studies have shown the importance of SHIP-1 in various immune cell subsets and have revealed a range of immune-mediated pathologies that are engendered due to loss of SHIP-1's regulatory activity, impelling investigations into the role of SHIP-1 in human disease. In this review, we provide an overview of the literature relating to the role of SHIP-1 in hematopoietic cell signaling and function, we summarize recent reports that highlight the dysregulation of the SHIP-1 pathway in cancers, autoimmune disorders and inflammatory diseases, and lastly we discuss the importance of SHIP-1 in restraining myeloid growth factor signaling.
SHIP-1是一种造血特异性肌醇磷酸酶,在包括生长因子、细胞因子、抗原、免疫球蛋白和Toll样受体激动剂等多种受体的下游被激活,发挥抑制性调控作用。虽然SHIP-1在所有免疫细胞中组成性表达,但其表达受到炎性和致癌性微小RNA miR-155的负调控。基因敲除小鼠研究表明SHIP-1在各种免疫细胞亚群中具有重要作用,并揭示了一系列由于SHIP-1调节活性丧失而导致的免疫介导病理,促使人们对SHIP-1在人类疾病中的作用进行研究。在这篇综述中,我们概述了与SHIP-1在造血细胞信号传导和功能中的作用相关的文献,总结了最近突出SHIP-1途径在癌症、自身免疫性疾病和炎性疾病中失调的报道,最后我们讨论了SHIP-1在抑制髓系生长因子信号传导中的重要性。