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胆固醇对趋化因子受体功能的调节作用:药物干预的新前景

Modulation of Chemokine Receptor Function by Cholesterol: New Prospects for Pharmacological Intervention.

作者信息

Legler Daniel F, Matti Christoph, Laufer Julia M, Jakobs Barbara D, Purvanov Vladimir, Uetz-von Allmen Edith, Thelen Marcus

机构信息

Biotechnology Institute Thurgau at the University of Konstanz, Kreuzlingen, Switzerland (D.F.L., C.M., J.M.L., B.D.J, V.P., E.U.A.); Konstanz Research School Chemical Biology, University of Konstanz, Germany (D.F.L., C.M., J.M.L); and Institute for Research in Biomedicine, Università della Svizzera italiana, Bellinzona, Switzerland (M.T.)

Biotechnology Institute Thurgau at the University of Konstanz, Kreuzlingen, Switzerland (D.F.L., C.M., J.M.L., B.D.J, V.P., E.U.A.); Konstanz Research School Chemical Biology, University of Konstanz, Germany (D.F.L., C.M., J.M.L); and Institute for Research in Biomedicine, Università della Svizzera italiana, Bellinzona, Switzerland (M.T.).

出版信息

Mol Pharmacol. 2017 Apr;91(4):331-338. doi: 10.1124/mol.116.107151. Epub 2017 Jan 12.

Abstract

Chemokine receptors are seven transmembrane-domain receptors belonging to class A of G-protein-coupled receptors (GPCRs). The receptors together with their chemokine ligands constitute the chemokine system, which is essential for directing cell migration and plays a crucial role in a variety of physiologic and pathologic processes. Given the importance of orchestrating cell migration, it is vital that chemokine receptor signaling is tightly regulated to ensure appropriate responses. Recent studies highlight a key role for cholesterol in modulating chemokine receptor activities. The steroid influences the spatial organization of GPCRs within the membrane bilayer, and consequently can tune chemokine receptor signaling. The effects of cholesterol on the organization and function of chemokine receptors and GPCRs in general include direct and indirect effects (Fig. 1). Here, we review how cholesterol and some key metabolites modulate functions of the chemokine system in multiple ways. We emphasize the role of cholesterol in chemokine receptor oligomerization, thereby promoting the formation of a signaling hub enabling integration of distinct signaling pathways at the receptor-membrane interface. Moreover, we discuss the role of cholesterol in stabilizing particular receptor conformations and its consequence for chemokine binding. Finally, we highlight how cholesterol accumulation, its deprivation, or cholesterol metabolites contribute to modulating cell orchestration during inflammation, induction of an adaptive immune response, as well as to dampening an anti-tumor immune response.

摘要

趋化因子受体是属于G蛋白偶联受体(GPCR)A类的七跨膜结构域受体。这些受体与其趋化因子配体共同构成趋化因子系统,该系统对于指导细胞迁移至关重要,并且在多种生理和病理过程中发挥关键作用。鉴于协调细胞迁移的重要性,严格调控趋化因子受体信号传导以确保适当反应至关重要。最近的研究突出了胆固醇在调节趋化因子受体活性中的关键作用。这种类固醇影响膜双层内GPCR的空间组织,因此可以调节趋化因子受体信号传导。一般来说,胆固醇对趋化因子受体以及GPCR的组织和功能的影响包括直接和间接影响(图1)。在这里,我们综述胆固醇和一些关键代谢物如何以多种方式调节趋化因子系统的功能。我们强调胆固醇在趋化因子受体寡聚化中的作用,从而促进信号枢纽的形成,使不同的信号通路能够在受体 - 膜界面整合。此外,我们讨论胆固醇在稳定特定受体构象中的作用及其对趋化因子结合的影响。最后,我们强调胆固醇积累、其缺乏或胆固醇代谢物如何在炎症期间调节细胞协调、诱导适应性免疫反应以及抑制抗肿瘤免疫反应中发挥作用。

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