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CXCR4:从 B 细胞发育到 B 细胞介导的疾病。

CXCR4: from B-cell development to B cell-mediated diseases.

机构信息

Department of Clinical Immunology and Internal Medicine, National Reference Center for Systemic Autoimmune Diseases (CNR RESO), Tertiary Center for Primary Immunodeficiency, Strasbourg University Hospital, Strasbourg, France

INSERM UMR - S1109, Institut thématique interdisciplinaire (ITI) de Médecine de Précision de Strasbourg, Transplantex NG, Fédération Hospitalo-Universitaire OMICARE, Fédération de Médecine Translationnelle de Strasbourg (FMTS), Strasbourg, France.

出版信息

Life Sci Alliance. 2024 Mar 22;7(6). doi: 10.26508/lsa.202302465. Print 2024 Jun.

Abstract

Chemokine receptors are members of the G protein-coupled receptor superfamily. The C-X-C chemokine receptor type 4 (CXCR4), one of the most studied chemokine receptors, is widely expressed in hematopoietic and immune cell populations. It is involved in leukocyte trafficking in lymphoid organs and inflammatory sites through its interaction with its natural ligand CXCL12. CXCR4 assumes a pivotal role in B-cell development, ranging from early progenitors to the differentiation of antibody-secreting cells. This review emphasizes the significance of CXCR4 across the various stages of B-cell development, including central tolerance, and delves into the association between CXCR4 and B cell-mediated disorders, from immunodeficiencies such as WHIM (warts, hypogammaglobulinemia, infections, and myelokathexis) syndrome to autoimmune diseases such as systemic lupus erythematosus. The potential of CXCR4 as a therapeutic target is discussed, especially through the identification of novel molecules capable of modulating specific pockets of the CXCR4 molecule. These insights provide a basis for innovative therapeutic approaches in the field.

摘要

趋化因子受体是 G 蛋白偶联受体超家族的成员。C-X-C 趋化因子受体 4(CXCR4)是研究最多的趋化因子受体之一,广泛表达于造血和免疫细胞群中。它通过与天然配体 CXCL12 的相互作用,参与淋巴细胞在淋巴器官和炎症部位的迁移。CXCR4 在 B 细胞发育的各个阶段(从早期祖细胞到分泌抗体的细胞分化)中都起着关键作用。本综述强调了 CXCR4 在 B 细胞发育的各个阶段的重要性,包括中枢耐受,并探讨了 CXCR4 与 B 细胞介导的疾病之间的关联,从免疫缺陷,如 WHIM(疣、低丙种球蛋白血症、感染和骨髓嗜中性粒细胞增多)综合征,到自身免疫性疾病,如系统性红斑狼疮。还讨论了 CXCR4 作为治疗靶点的潜力,特别是通过鉴定能够调节 CXCR4 分子特定口袋的新型分子。这些见解为该领域的创新治疗方法提供了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4868/10961644/13c497ac3c3f/LSA-2023-02465_Fig1.jpg

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