Evidence map›Paper›PMID 9566869›Full record

ArticleMolecular and cellular biology1998

Activation of the small GTPase Ral in platelets.

R M Wolthuis, B Franke, M van Triest, B Bauer, R H Cool, J H Camonis, J W Akkerman, J L Bos

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

52 citing papers in PubMed, 142 citations in OpenAlex.

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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

8 authors at 4 institutions in 5 countries.

R M WolthuisLaboratory for Physiological Chemistry, Utrecht University, The Netherlands.
B Franke
M van Triest
B Bauer
R H Cool
J H Camonis
J W Akkerman
J L Bos
University of Applied Sciences Utrecht · NLMax Planck Society · DEPhysiological Society · GBInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ral is a ubiquitously expressed Ras-like small GTPase which is abundantly present in human platelets. The biological function of Ral and the signaling pathway in which Ral is involved are largely unknown. Here we describe a novel method to measure Ral activation utilizing the Ral binding domain of the putative Ral effector RLIP76 as an activation-specific probe. With this assay we investigated the signaling pathway that leads to Ral activation in human platelets. We found that Ral is rapidly activated after stimulation with various platelet agonists, including alpha-thrombin. In contrast, the platelet antagonist prostaglandin I2 inhibited alpha-thrombin-induced Ral activation. Activation of Ral by alpha-thrombin could be inhibited by depletion of intracellular Ca2+, whereas the induction of intracellular Ca2+ resulted in the activation of Ral. Our results show that Ral can be activated by extracellular stimuli. Furthermore, we show that increased levels of intracellular Ca2+ are sufficient for Ral activation in platelets. This activation mechanism correlates with the activation mechanism of the small GTPase Rap1, a putative upstream regulator of Ral guanine nucleotide exchange factors.

Indexed as

ATP-Binding Cassette TransportersGTPase-Activating ProteinsBlood PlateletsCalciumCarrier ProteinsEnzyme ActivationEpoprostenolGTP-Binding ProteinsGTP PhosphohydrolasesGuanosine TriphosphateHumansPeptide FragmentsPlatelet ActivationProtein Bindingral GTP-Binding Proteinsrap GTP-Binding ProteinsATP-Binding Cassette TransportersCalciumCarrier ProteinsEpoprostenolGTPase-Activating ProteinsGTP-Binding ProteinsGTP PhosphohydrolasesGuanosine TriphosphatePeptide FragmentsRALBP1 protein, humanral GTP-Binding Proteinsrap GTP-Binding ProteinsThrombin

Identifiers

PMID9566869
PMCPMC110628
OpenAlexW2156875265

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.