Selective targeting of mu opioid receptors to primary cilia

被引:3
|
作者
Fagan, Rita R. [1 ]
Lee, David F. [2 ]
Geron, Matan [2 ]
Scherrer, Gregory [2 ,3 ]
von Zastrow, Mark [1 ]
Ehrlich, Aliza T. [1 ]
机构
[1] Univ Calif San Francisco, Dept Psychiat & Behav Sci, San Francisco, CA 94158 USA
[2] Univ North Carolina Chapel Hill, UNC Neurosci Ctr, Dept Cell Biol & Physiol, Dept Pharmacol, Chapel Hill, NC 27599 USA
[3] New York Stem Cell Fdn, Chapel Hill, NC 27599 USA
来源
CELL REPORTS | 2024年 / 43卷 / 05期
基金
美国国家卫生研究院;
关键词
TRAFFICKING; PLATFORM; SIGNAL; IDENTIFICATION; LOCALIZATION; PATHWAY;
D O I
10.1016/j.celrep.2024.114164
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Opioid receptors are therapeutically important G protein -coupled receptors (GPCRs) with diverse neuromodulatory effects. The functional consequences of opioid receptor activation are known to depend on receptor location in the plasma membrane, but mechanisms mediating selective localization of receptors to any particular membrane domain remain elusive. Here, we demonstrate the targeting of the mu opioid receptor (MOR) to the primary cilium, a discrete microdomain of the somatic plasma membrane, both in vivo and in cultured cells. We further show that ciliary targeting is specific to MORs, requires a 17 -residue sequence unique to the MOR cytoplasmic tail, and additionally requires the Tubby -like protein 3 (TULP3) ciliary adaptor protein. Our results reveal the potential for opioid receptors to undergo selective localization to the primary cilium. We propose that ciliary targeting is mediated through an elaboration of the recycling pathway, directed by a specific C -terminal recycling sequence in cis and requiring TULP3 in trans .
引用
收藏
页数:17
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