Department of Pharmacology, University of Montreal, Montreal, Quebec, H3T 1J4, Canada.
Ste-Justine Hospital, Montreal, Quebec, H3T 1C5, Canada.
Cell Mol Life Sci. 2018 Jun;75(12):2257-2271. doi: 10.1007/s00018-017-2732-5. Epub 2017 Dec 29.
Soon after internalization delta opioid receptors (DOPrs) are committed to the degradation path by G protein-coupled receptor (GPCR)-associated binding protein. Here we provide evidence that this classical post-endocytic itinerary may be rectified by downstream sorting decisions which allow DOPrs to regain to the membrane after having reached late endosomes (LE). The LE sorting mechanism involved ESCRT accessory protein Alix and the TIP47/Rab9 retrieval complex which supported translocation of the receptor to the TGN, from where it subsequently regained the cell membrane. Preventing DOPrs from completing this itinerary precipitated acute analgesic tolerance to the agonist DPDPE, supporting the relevance of this recycling path in maintaining the analgesic response by this receptor. Taken together, these findings reveal a post-endocytic itinerary where GPCRs that have been sorted for degradation can still recycle to the membrane.
内化后,δ 阿片受体(DOPrs)通过与 G 蛋白偶联受体(GPCR)相关的结合蛋白被定向到降解途径。在这里,我们提供的证据表明,这种经典的胞内体后途径可以通过下游分选决定进行修正,使 DOPrs 在到达晚期内体(LE)后能够重新回到细胞膜上。涉及 ESCRT 辅助蛋白 Alix 和 TIP47/Rab9 回收复合物的 LE 分选机制支持受体向 TGN 的易位,受体随后从 TGN 重新获得细胞膜。阻止 DOPrs 完成这一途径会导致激动剂 DPDPE 引发急性镇痛耐受,支持这种受体通过这种再循环途径维持镇痛反应的相关性。总之,这些发现揭示了一种胞内体后途径,其中已被分选进行降解的 GPCR 仍可再循环到细胞膜。