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Functional coupling of mu-receptor-Galphai-tethered proteins in AtT20 cells.

机译:在AtT20细胞中的mu受体Galphai拴系蛋白的功能偶联。

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Opioid efficacy on mu-receptor may be influenced by various Gi/o-G-protein subunits interacting with intracellular face of receptor. Pertussis toxin-insensitive Galphai1 and Galphai2 subunits tethered with mu-receptor were stably transfected into AtT20 cells to (i) determine coupling of different alpha-subunits on opioid efficacy, and (ii) determine coupling to downstream effectors, for example, calcium and potassium channels. After pertussis toxin, stimulation of [35S]GTP-gamma-S incorporation persisted. Both constructs were able to couple to native calcium and potassium channels, with endomorphins 1 and 2 equally effective. However, pertussis toxin abolished opioid actions on calcium and potassium channels suggesting strong coupling to endogenous G-proteins, and that differences in coupling efficacy to Galphai1 and Galphai2 previously observed are restricted to initial step of signaling cascade.
机译:阿片样物质对mu受体的功效可能受到与受体细胞内表面相互作用的各种Gi / o-G蛋白亚基的影响。将与mu受体束缚的百日咳毒素不敏感的Galphai1和Galphai2亚基稳定转染到AtT20细胞中,以(i)确定不同α-亚基对阿片样物质功效的偶联,和(ii)确定与下游效应物的偶联,例如钙和钾渠道。百日咳毒素后,仍持续刺激[35S]GTP-γ-S掺入。两种构建体均能够偶联天然钙和钾通道,内啡肽1和2等效。然而,百日咳毒素取消了对钙和钾通道的阿片样物质作用,表明与内源性G蛋白的强耦合,并且先前观察到的与Galphai1和Galphai2的耦合功效的差异仅限于信号级联的初始步骤。

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