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Cell Reports
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Cell Reports
Article . 2024
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Selective Targeting of Mu Opioid Receptors to Primary Cilia

Authors: Rita R. Fagan; David F. Lee; Matan Geron; Grégory Scherrer; Mark von Zastrow; Aliza T. Ehrlich;

Selective Targeting of Mu Opioid Receptors to Primary Cilia

Abstract

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.

Country
United States
Keywords

QH301-705.5, 1.1 Normal biological development and functioning, brain, Medical Physiology, Receptors, Opioid, mu, 610, Opioid, recycling, neuronal, Article, TULP3, Substance Misuse, Mice, GPCR, Receptors, 2.1 Biological and endogenous factors, Animals, Humans, G protein-coupled receptor, Cilia, Biology (General), mouse, MOR, Neurosciences, NEURONAL, Biological Sciences, Opioids, Biological sciences, Protein Transport, HEK293 Cells, mu, CP: Cell biology, Biochemistry and Cell Biology, Generic health relevance, Drug Abuse (NIDA only), primary cilium

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    popularity
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    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
17
Top 10%
Average
Top 10%
Green
gold