Evidence map›Paper›PMID 17878312›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

Phospholipase Cepsilon is a nexus for Rho and Rap-mediated G protein-coupled receptor-induced astrocyte proliferation.

Simona Citro, Sundeep Malik, Emily A Oestreich, Julie Radeff-Huang, Grant G Kelley, Alan V Smrcka, Joan Heller Brown

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing 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

51 citing papers in PubMed, 74 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Frontiers in genetics · 2021
    Article
  8. Article
  9. Article
  10. Review
  11. BioMed research international · 2019
    Article
  12. Article
  13. Article
  14. Article
  15. Selective coupling of the S1PJournal of molecular and cellular cardiology · 2017
    Article
  16. Phospholipase C-ε signaling mediates endothelial cell inflammation and barrier disruption in acute lung injury.American journal of physiology. Lung cellular and molecular physiology · 2016
    Article
  17. Article
  18. Article
  19. Review
  20. PLCε mediated sustained signaling pathways.Advances in biological regulation · 2015
    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

7 authors at 3 institutions in 1 country.

Simona CitroDepartment of Pharmacology, University of California at San Diego, La Jolla, CA 92093, USA.
Sundeep Malik
Emily A Oestreich
Julie Radeff-Huang
Grant G Kelley
Alan V Smrcka
Joan Heller Brown
University of California, San Diego · USUniversity of Rochester · USSUNY Upstate Medical University · US

Funding

TRAINING PROGRAM IN ORAL SCIENCET32DE007202 · NIDCR · UNIVERSITY OF ROCHESTER · PI QUIVEY, ROBERT G · 1990 to 2010
$5.5M
SIGNAL TRANSDUCTION BY G PROTEINR01GM053536 · NIGMS · UNIVERSITY OF ROCHESTER · PI SMRCKA, ALAN V. · 1996 to 2018
$4.9M
THROMBIN, GALPHA12, AND RHO AND CELL GROWTHR01GM036927 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BROWN, JOAN HELLER · 1986 to 2012
$3.4M
Rho- and GPCR-mediated signaling through novel cellular effectorsR56GM036927 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BROWN, JOAN HELLER · 2008 to 2008
$302k
NIDCR NIH HHS T32 DE007202NIDCR NIH HHS T32 DE07202NIGMS NIH HHS GM 36927NIGMS NIH HHS GM 53536NIGMS NIH HHS R01 GM036927NIGMS NIH HHS R01 GM053536NIGMS NIH HHS R56 GM036927
6 · The paper itself

Abstract

Phospholipase Cepsilon (PLCepsilon) has been suggested to transduce signals from small GTPases, but its biological function has not yet been clarified. Using astrocytes from PLCepsilon-deficient mice, we demonstrate that endogenous G protein-coupled receptors (GPCRs) for lysophosphatidic acid, sphingosine 1-phosphate, and thrombin regulate phosphoinositide hydrolysis primarily through PLCepsilon. Stimulation by lysophospholipids occurs through G(i), whereas thrombin activates PLC through Rho. Further studies reveal that PLCepsilon is required for thrombin- but not LPA-induced sustained ERK activation and DNA synthesis, providing a novel mechanism for GPCR and Rho signaling to cell proliferation. The requirement for PLCepsilon in this pathway can be explained by its role as a guanine nucleotide exchange factor for Rap1. Thus, PLCepsilon serves to transduce mitogenic signals through a mechanism distinct from its role in generation of PLC-derived second messengers.

Indexed as

AnimalsAstrocytesCarbacholCell ProliferationGenotypeGTP PhosphohydrolasesLysophospholipidsMiceMice, KnockoutMice, TransgenicPhosphoinositide Phospholipase Crap GTP-Binding ProteinsReceptors, G-Protein-Coupledrho GTP-Binding ProteinsSignal TransductionType C PhospholipasesCarbacholGTP PhosphohydrolasesLysophospholipidsPhosphoinositide Phospholipase Cphospholipase C epsilonrap GTP-Binding ProteinsReceptors, G-Protein-Coupledrho GTP-Binding ProteinsType C Phospholipases

Identifiers

PMID17878312
PMCPMC2000505
OpenAlexW1994108205

What OpenQuestion holds

Textmetadata
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.