Evidence map›Paper›PMID 23096711›Full record

ArticleThe Journal of investigative dermatology2013

Lysophosphatidic acid promotes cell migration through STIM1- and Orai1-mediated Ca2+(i) mobilization and NFAT2 activation.

Ralph Jans, Laura Mottram, Darren L Johnson, Anna M Brown, Stephen Sikkink, Kehinde Ross, Nick J Reynolds

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.9field-weighted citation impact, top 17% 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

15 citing papers in PubMed, 34 citations in OpenAlex.

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  14. ORAI1 calcium channel orchestrates skin homeostasis.Proceedings of the National Academy of Sciences of the United States of America · 2013
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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 1 institution in 1 country.

Ralph JansDermatological Sciences, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK.
Laura MottramDermatological Sciences, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK.
Darren L JohnsonDermatological Sciences, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK.
Anna M BrownDermatological Sciences, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK.
Stephen SikkinkDermatological Sciences, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK.
Kehinde RossDermatological Sciences, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK.
Nick J ReynoldsDermatological Sciences, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK. Electronic address: n.j.reynolds@ncl.ac.uk.
Newcastle University · GB

Funding

Medical Research Council G0502242Wellcome Trust 061178
6 · The paper itself

Abstract

Lysophosphatidic acid (LPA) enhances cell migration and promotes wound healing in vivo, but the intracellular signaling pathways regulating these processes remain incompletely understood. Here we investigated the involvement of agonist-induced Ca(2+) entry and STIM1 and Orai1 proteins in regulating nuclear factor of activated T cell (NFAT) signaling and LPA-induced keratinocyte cell motility. As monitored by Fluo-4 imaging, stimulation with 10 μM LPA in 60 μM Ca(2+)(o) evoked Ca(2+)(i) transients owing to store release, whereas addition of LPA in physiological 1.2 mM Ca(2+)(o) triggered store release coupled to extracellular Ca(2+) entry. Store-operated Ca(2+) entry (SOCE) was blocked by the SOCE inhibitor diethylstilbestrol (DES), STIM1 silencing using RNA interference (RNAi), and expression of dominant/negative Orai1(R91W). LPA induced significant NFAT activation as monitored by nuclear translocation of green fluorescent protein-tagged NFAT2 and a luciferase reporter assay, which was impaired by DES, expression of Orai1(R91W), and inhibition of calcineurin using cyclosporin A (CsA). By using chemotactic migration assays, LPA-induced cell motility was significantly impaired by STIM1, CsA, and NFAT2 knockdown using RNAi. These data indicate that in conditions relevant to epidermal wound healing, LPA induces SOCE and NFAT activation through Orai1 channels and promotes cell migration through a calcineurin/NFAT2-dependent pathway.

Indexed as

CalcineurinCalciumCalcium ChannelsCalcium SignalingCell MovementCells, CulturedFemaleHumansKeratinocytesLysophospholipidsMaleMembrane ProteinsNeoplasm ProteinsNFATC Transcription FactorsORAI1 ProteinRNA InterferenceCalcineurinCalciumCalcium Channelslysophosphatidic acidLysophospholipidsMembrane ProteinsNeoplasm ProteinsNFATC1 protein, humanNFATC Transcription FactorsORAI1 ProteinORAI1 protein, humanSTIM1 protein, humanStromal Interaction Molecule 1

Identifiers

PMID23096711
PMCPMC3572452
OpenAlexW2079996915

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.