Evidence map›Paper›PMID 26012717›Full record

ArticleStem cells (Dayton, Ohio)2015

Morphine Promotes Astrocyte-Preferential Differentiation of Mouse Hippocampal Progenitor Cells via PKCε-Dependent ERK Activation and TRBP Phosphorylation.

Chi Xu, Hui Zheng, Horace H Loh, Ping-Yee Law

Open access · greenAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. MicroRNAs: From Mechanism to Organism.Frontiers in cell and developmental biology · 2020
    Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Effects of addictive drugs on adult neural stem/progenitor cells.Cellular and molecular life sciences : CMLS · 2016
    Review
  15. Review
  16. Article
  17. Mystery of Trbp, tale of a RBP in the miRNA pathway.Cell cycle (Georgetown, Tex.) · 2015
    Article
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

4 authors at 2 institutions in 2 countries.

Chi XuDepartment of Pharmacology, University of Minnesota Medical School, Minneapolis, Minnesota, USA.
Hui ZhengStem Cell and Cancer Biology Group, Key Laboratory of Regenerative Biology, South China Institute for Stem Cell Biology and Regenerative Medicine, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, People's Republic of China.
Horace H LohDepartment of Pharmacology, University of Minnesota Medical School, Minneapolis, Minnesota, USA.
Ping-Yee LawDepartment of Pharmacology, University of Minnesota Medical School, Minneapolis, Minnesota, USA.
University of Minnesota Medical Center · USGuangzhou Institutes of Biomedicine and Health · CN

Funding

Studies on the the mechanism of OPRM1 biased agonism and in vivo consequences: DiR01DA031442 · NIDA · UNIVERSITY OF MINNESOTA · PI LAW, PING-YEE · 2012 to 2016
$1.9M
NIDA NIH HHS DA031442-03NIDA NIH HHS R01 DA031442
6 · The paper itself

Abstract

Previously we have shown that morphine regulates adult neurogenesis by modulating miR-181a maturation and subsequent hippocampal neural progenitor cell (NPC) lineages. Using NPCs cultured from PKCε or β-arrestin2 knockout mice and the MAPK/ERK kinase inhibitor U0126, we demonstrate that regulation of NPC differentiation via the miR-181a/Prox1/Notch1 pathway exhibits ligand-dependent selectivity. In NPCs, morphine and fentanyl activate ERK via the PKCε- and β-arrestin-dependent pathways, respectively. After fentanyl exposure, the activated phospho-ERK translocates to the nucleus. Conversely, after morphine treatment, phospho-ERK remains in the cytosol and is capable of phosphorylating TAR RNA-binding protein (TRBP), a cofactor of Dicer. This augments Dicer activity and promotes the maturation of miR-181a. Furthermore, using NPCs transfected with wild-type TRBP, SΔA, and SΔD TRBP mutants, we confirmed the crucial role of TRBP phosphorylation in Dicer activity, miR-181a maturation, and finally the morphine-induced astrocyte-preferential differentiation of NPCs. Thus, morphine modulates the lineage-specific differentiation of NPCs by PKCε-dependent ERK activation with subsequent TRBP phosphorylation and miR-181a maturation.

Indexed as

AnimalsAstrocytesCell DifferentiationHippocampusMaleMAP Kinase Signaling SystemMiceMice, Inbred C57BLMice, KnockoutMorphineNeural Stem CellsPhosphorylationProtein Kinase C-epsilonRNA-Binding ProteinsTrans-Activation Responsive RNA-Binding ProteinMorphineProtein Kinase C-epsilonRNA-Binding ProteinsTrans-Activation Responsive RNA-Binding ProteinAdult stem cellsCell signalingMAPKmiRNANeural differentiationNeural stem cellProgenitor cellsSignal transduction

Identifiers

PMID26012717
PMCPMC4549172
OpenAlexW1581255866

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.