Evidence map›Paper›PMID 22638989›Full record

ArticleGlia2012

β-arrestin 2-dependent activation of ERK1/2 is required for ADP-induced paxillin phosphorylation at Ser(83) and microglia chemotaxis.

Sang-Hyun Lee, Ryan Hollingsworth, Hyeok-Yil Kwon, Narae Lee, Chang Y Chung

Abstract read
In one paragraph

Article in Glia, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

14 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Review
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  7. Article
  8. P2YFrontiers in pharmacology · 2018
    Review
  9. Review
  10. Article
  11. Review
  12. Validation of Flow Cytometry and Magnetic Bead-Based Methods to Enrich CNS Single Cell Suspensions for Quiescent Microglia.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2015
    Article
  13. Microglia is a key player in the reduction of stroke damage promoted by the new antithrombotic agent ticagrelor.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2014
    Article
  14. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Sang-Hyun LeeDepartment of Pharmacology, Vanderbilt University Medical Center, Nashville, TN 37232-6600, USA.
Ryan Hollingsworth
Hyeok-Yil Kwon
Narae Lee
Chang Y Chung
Vanderbilt University Medical Center · USHallym University · KR

Funding

Spatial Regulation of Cytoskeleton During ChemotaxisR01GM068097 · NIGMS · VANDERBILT UNIVERSITY · PI CHUNG, CHANG Y · 2003 to 2012
$2.7M
NIGMS NIH HHS GM68097NIGMS NIH HHS R01 GM068097
6 · The paper itself

Abstract

Microglia play crucial roles in increased inflammation in the central nervous system upon brain injuries and diseases. Extracellular ADP has been reported to induce microglia chemotaxis and membrane ruffle formation through P2Y(12) receptor. In this study, we examined the role of ERK1/2 activation in ADP-induced microglia chemotaxis. ADP stimulation increases the phosphorylation of extracellular signal-regulated kinase 1/2 (ERK1/2) and paxillin phosphorylation at Tyr(31) and Ser(83) . Inhibition of ERK1/2 significantly inhibited paxillin phosphorylation at Ser(83) and the retraction of membrane ruffles, causing inefficient chemotaxis. Close examination of dynamics of focal adhesion (FA) formation with green fluorescent protein-paxillin revealed that the disassembly of FAs in U0126-treated cells was significantly impaired. Depletion of β-Arrestin 2 (β-Arr2) with short hairpin RNA markedly reduced the phosphorylation of ERK1/2 and Pax/Ser(83) , indicating that β-Arr2 is required for ERK1/2 activation upon ADP stimulation. A large fraction of phosphorylated ERK1/2 and β-Arr2 were translocated and co-localized at focal contacts in the newly forming lamellipodia. Examination of kinetics and rate constant of paxillin formation and disassembly revealed that the phosphorylation of paxillin at Tyr(31) by c-Src appears to be involved in adhesion formation upon ADP stimulation while Ser(83) required for adhesion disassembly.

Indexed as

Adenosine DiphosphateAnimalsArrestinsbeta-Arrestin 2beta-ArrestinsCell AdhesionCell LineChemotaxisFocal AdhesionsMAP Kinase Signaling SystemMiceMicrogliaPaxillinPhosphorylationAdenosine DiphosphateArrb2 protein, mouseArrestinsbeta-Arrestin 2beta-ArrestinsPaxillin

Identifiers

PMID22638989
PMCPMC3984973
OpenAlexW1973680268

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.