LILRB4在免疫应答中的分子调控机制。

IF 1.5 4区 医学 Q4 IMMUNOLOGY Central European Journal of Immunology Pub Date : 2023-01-01 DOI:10.5114/ceji.2023.125238
Haiyin Liu, Jun Yang, Jing Zhang, Peiyue Zhang, Mengting Zhang, Chaojun Yang, Li Liu, Cuiyuan Huang, Wei Wang, Yuhong Zhai, Jian Yang
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引用次数: 0

摘要

免疫性疾病是由免疫调节失衡引起的。这种不平衡受到许多因素的调节,既有消极的因素,也有积极的因素。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)的一个成员。lilr在多种免疫细胞表面组成性地表达,这些细胞通过多种细胞质免疫受体酪氨酸抑制基序(ITIMs)或免疫受体酪氨酸激活基序(ITAMs)与膜受体结合,发出信号。LILRB4通过ITIM将src同源结构域2型酪氨酸磷酸酶1或2 (SHP-1或SHP-2)募集到细胞膜内。此外,许多因素可以诱导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调控作用。本文拟阐述LILRB4的结构和功能,以及其在免疫细胞中的调节因子和受体,为免疫疾病的治疗提供理论依据。
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Molecular regulatory mechanism of LILRB4 in the immune response.

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.

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来源期刊
CiteScore
3.00
自引率
0.00%
发文量
17
审稿时长
6-12 weeks
期刊介绍: Central European Journal of Immunology is a English-language quarterly aimed mainly at immunologists.
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