Steele Amber D, Szabo Imre, Bednar Filip, Rogers Thomas J
Department of Microbiology and Immunology, Fels Institute for Cancer Research and Molecular Biology, Center for Substance Abuse Research, Temple University School of Medicine, Philadelphia, PA 19140, USA.
Cytokine Growth Factor Rev. 2002 Jun;13(3):209-22. doi: 10.1016/s1359-6101(02)00007-2.
The opioid and chemokine receptors are both members of the seven transmembrane G protein-coupled receptor (GPCR) superfamily. Desensitization is believed to be a major element of the regulation of the function of these receptors, and recent findings suggest that both agonist-dependent (homologous) desensitization and heterologous desensitization can control receptor activity. The cross-desensitization between opioid and chemokine receptors has significant implications for our understanding of both the regulation of leukocyte trafficking, as well as the regulation of chemokine receptor function in inflammatory disease states. We also review findings which suggest that pro-inflammatory chemokine receptor-induced heterologous desensitization of opioid receptors has important implications for the regulation of opioid receptor function in the nervous system.
阿片类受体和趋化因子受体均属于七跨膜G蛋白偶联受体(GPCR)超家族。脱敏被认为是这些受体功能调节的一个主要因素,最近的研究结果表明,激动剂依赖性(同源)脱敏和异源脱敏均可控制受体活性。阿片类受体与趋化因子受体之间的交叉脱敏对于我们理解白细胞迁移的调节以及炎症疾病状态下趋化因子受体功能的调节具有重要意义。我们还综述了一些研究结果,这些结果表明促炎趋化因子受体诱导的阿片类受体异源脱敏对神经系统中阿片类受体功能的调节具有重要意义。