Evidence map›Paper›PMID 20410114›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2010

Nerve growth factor-regulated emergence of functional delta-opioid receptors.

Bihua Bie, Zhi Zhang, You-Qing Cai, Wei Zhu, Yong Zhang, Jaile Dai, Charles J Lowenstein, Edward J Weinman, Zhizhong Z Pan

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.7field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. The Delta-Opioid Receptor; a Target for the Treatment of Pain.Frontiers in molecular neuroscience · 2020
    Review
  7. Article
  8. Article
  9. Article
  10. Spatial encoding of GPCR signaling in the nervous system.Current opinion in cell biology · 2019
    Review
  11. Article
  12. Article
  13. Article
  14. Pharmacogenetics of Methadone Response.Molecular diagnosis & therapy · 2018
    Review
  15. Article
  16. Article
  17. A PTEN-Regulated Checkpoint Controls Surface Delivery of δ Opioid Receptors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  18. Article
  19. Regulation of αScientific reports · 2016
    Article
  20. Molecular Pharmacology of δ-Opioid Receptors.Pharmacological reviews · 2016
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Bihua BieDepartment of Anesthesiology, The University of Texas-MD Anderson Cancer Center, Houston, Texas 77030, USA.
Zhi Zhang
You-Qing Cai
Wei Zhu
Yong Zhang
Jaile Dai
Charles J Lowenstein
Edward J Weinman
Zhizhong Z Pan
The University of Texas MD Anderson Cancer Center · USJohns Hopkins Medicine · USUniversity of Maryland, Baltimore · US

Funding

Synaptic mechanisms for interactions of chronic pain and opioid addictionR01DA027541 · NIDA · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI PAN, ZHIZHONG Z. · 2009 to 2013
$1.7M
Delta-Opioid Receptor Trafficking and Pain InhibitionR01DA023069 · NIDA · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI PAN, ZHIZHONG Z. · 2008 to 2012
$1.5M
Impact of pain on sensitivity to opioid rewardR21DA025826 · NIDA · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI PAN, ZHIZHONG Z. · 2009 to 2010
$421k
NIDA NIH HHS DA023069NIDA NIH HHS DA025826NIDA NIH HHS R01 DA023069NIDA NIH HHS R01 DA027541NIDA NIH HHS R21 DA025826
6 · The paper itself

Abstract

Sorting of intracellular G-protein-coupled receptors (GPCRs) either to lysosomes for degradation or to plasma membrane for surface insertion and functional expression is a key process regulating signaling strength of GPCRs across the plasma membrane in adult mammalian cells. However, little is known about the molecular mechanisms governing the dynamic process of receptor sorting to the plasma membrane for functional expression under normal and pathological conditions. In this study, we demonstrate that delta-opioid receptor (DOPr), a GPCR constitutively targeted to intracellular compartments, is driven to the surface membrane of central synaptic terminals and becomes functional by the neurotrophin nerve growth factor (NGF) in native brainstem neurons. The NGF-triggered DOPr translocation is predominantly mediated by the signaling pathway involving the tyrosine receptor kinase A, Ca(2+)-mobilizing phospholipase C, and Ca(2+)/calmodulin-dependent protein kinase II. Importantly, it requires interactions with the cytoplasmic sorting protein NHERF-1 (Na(+)/H(+) exchange regulatory factor-1) and N-ethyl-maleimide-sensitive factor-regulated exocytosis. In addition, this NGF-mediated mechanism is likely responsible for the emergence of functional DOPr induced by chronic opioids. Thus, NGF may function as a key molecular switch that redirects the sorting of intracellularly targeted DOPr to plasma membrane, resulting in new functional DOPr on central synapses under chronic opioid conditions.

Indexed as

AnimalsExcitatory Postsynaptic PotentialsMaleMiceMice, KnockoutMorphineNerve Growth FactorRatsRats, WistarReceptors, Opioid, deltaMorphineNerve Growth FactorReceptors, Opioid, delta

Identifiers

PMID20410114
PMCPMC2865237
OpenAlexW2037513247

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.