Delta opioid receptors recycle to the membrane after sorting to the degradation path

被引:14
作者
Charfi, Iness [1 ,4 ]
Abdallah, Khaled [2 ]
Gendron, Louis [2 ]
Pineyro, Graciela [1 ,3 ,4 ]
机构
[1] Univ Montreal, Dept Pharmacol, Montreal, PQ H3T 1J4, Canada
[2] Univ Sherbrooke, Dept Pharmacol Physiol, Sherbrooke, PQ J1H 5N4, Canada
[3] Univ Montreal, Dept Psychiat, Montreal, PQ H3T 1J4, Canada
[4] Ste Justine Hosp, Montreal, PQ H3T 1C5, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
Delta opioid receptor; Recycling; Analgesic tolerance; Trans Golgi network; Rab9/TIP47; complex; Alix; PROTEIN-COUPLED RECEPTORS; MANNOSE 6-PHOSPHATE RECEPTOR; IN-VIVO; SELECTIVE CARGO; GOLGI; TRAFFICKING; TRANSPORT; ENDOSOMES; UBIQUITINATION; ACTIN;
D O I
10.1007/s00018-017-2732-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:2257 / 2271
页数:15
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