Liu Haiyin, Yang Jun, Zhang Jing, Zhang Peiyue, Zhang Mengting, Yang Chaojun, Liu Li, Huang Cuiyuan, Wang Wei, Zhai Yuhong, Yang Jian
Department of Cardiology, The First College of Clinical Medical Science, China Three Gorges University, Yichang, China.
Institute of Cardiovascular Diseases, China Three Gorges University, Yichang, China.
Cent Eur J Immunol. 2023;48(1):43-47. doi: 10.5114/ceji.2023.125238. Epub 2023 Feb 23.
Immune diseases are caused by the imbalance of immune regulation. This imbalance is regulated by many factors, both negative and positive. Leukocyte immunoglobulin-like receptor B4 (LILRB4) is a member of leukocyte immunoglobulin-like receptors (LILRs). LILRs are expressed constitutively on the surface of multiple immune cells which associate with membrane adaptors to signal through multi- ple cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs) or immunoreceptor tyro-sine-based activation motifs (ITAMs). Through ITIM, LILRB4 could recruit the src homology domain type-2-containing tyrosine phosphatase 1 or 2 (SHP-1 or SHP-2) into the cell membrane. In addition, many factors can induce the expression of LILRB4, such as vitamin D, interferon and so on. Studies have demonstrated that LILRB4 had a negative regulatory role in various of immune diseases. The present review intends to expound the structure and function of LILRB4, as well as its regulators and receptors in the immune cells, so as to provide a theoretical basis for immune disease therapy.
免疫疾病是由免疫调节失衡引起的。这种失衡受多种因素调节,包括负性和正性因素。白细胞免疫球蛋白样受体B4(LILRB4)是白细胞免疫球蛋白样受体(LILRs)的成员之一。LILRs在多种免疫细胞表面组成性表达,这些免疫细胞与膜衔接蛋白结合,通过多个基于免疫受体酪氨酸的抑制性基序(ITIMs)或基于免疫受体酪氨酸的激活基序(ITAMs)进行信号传导。通过ITIM,LILRB4可将含src同源结构域2的酪氨酸磷酸酶1或2(SHP-1或SHP-2)募集到细胞膜中。此外,许多因素可诱导LILRB4的表达,如维生素D、干扰素等。研究表明,LILRB4在多种免疫疾病中具有负性调节作用。本综述旨在阐述LILRB4的结构和功能,以及其在免疫细胞中的调节因子和受体,从而为免疫疾病治疗提供理论依据。