Evidence map›Paper›PMID 23788641›Full record

ArticleThe Journal of biological chemistry2013

Control of voltage-gated potassium channel Kv2.2 expression by pyruvate-isocitrate cycling regulates glucose-stimulated insulin secretion.

Mette V Jensen, Jonathan M Haldeman, Hengtao Zhang, Danhong Lu, Mark O Huising, Wylie W Vale, Hans E Hohmeier, Paul Rosenberg, Christopher B Newgard

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 23 citations in OpenAlex.

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  12. KThe Journal of biological chemistry · 2018
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  18. Review
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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

9 authors at 2 institutions in 2 countries.

Mette V JensenDuke Institute of Molecular Physiology, Duke University Medical Center, Durham, North Carolina 27704, USA.
Jonathan M Haldeman
Hengtao Zhang
Danhong Lu
Mark O Huising
Wylie W Vale
Hans E Hohmeier
Paul Rosenberg
Christopher B Newgard
Duke Medical Center · USClayton Foundation · CH

Funding

TARGETED DISRUPTION OF NEUROENDOCRINE GENESP01DK026741 · NIDDK · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI RIVIER, JEAN E · 1986 to 2014
$31.6M
ORGANIZATION AND FUNCTIONS OF CELLULAR STRUCTUREST32GM007184 · NIGMS · DUKE UNIVERSITY · PI JINKS-ROBERTSON, SUE · 1985 to 2019
$18.2M
NIDDK NIH HHS DK026741NIDDK NIH HHS DK42583NIDDK NIH HHS P01 DK026741NIGMS NIH HHS T32 GM007184
6 · The paper itself

Abstract

Recent studies have shown that the pyruvate-isocitrate cycling pathway, involving the mitochondrial citrate/isocitrate carrier and the cytosolic NADP-dependent isocitrate dehydrogenase (ICDc), is involved in control of glucose-stimulated insulin secretion (GSIS). Here we demonstrate that pyruvate-isocitrate cycling regulates expression of the voltage-gated potassium channel family member Kv2.2 in islet β-cells. siRNA-mediated suppression of ICDc, citrate/isocitrate carrier, or Kv2.2 expression impaired GSIS, and the effect of ICDc knockdown was rescued by re-expression of Kv2.2. Moreover, chronic exposure of β-cells to elevated fatty acids, which impairs GSIS, resulted in decreased expression of Kv2.2. Surprisingly, knockdown of ICDc or Kv2.2 increased rather than decreased outward K(+) current in the 832/13 β-cell line. Immunoprecipitation studies demonstrated interaction of Kv2.1 and Kv2.2, and co-overexpression of the two channels reduced outward K(+) current compared with overexpression of Kv2.1 alone. Also, siRNA-mediated knockdown of ICDc enhanced the suppressive effect of the Kv2.1-selective inhibitor stromatoxin1 on K(+) currents. Our data support a model in which a key function of the pyruvate-isocitrate cycle is to maintain levels of Kv2.2 expression sufficient to allow it to serve as a negative regulator of Kv channel activity.

Indexed as

AnimalsGene Expression RegulationGlucoseInsulinInsulin-Secreting CellsInsulin SecretionIon Channel GatingIon TransportIsocitrate DehydrogenaseIsocitratesMaleModels, BiologicalPeptidesPotassiumPyruvic AcidRatsGlucoseInsulinIsocitrate Dehydrogenaseisocitrate dehydrogenase (NADP+)Isocitratesisocitric acidPeptidesPotassiumPyruvic AcidShab Potassium ChannelsSpider Venomsstromatoxin protein, Stromatopelma calceataDiabetesGlucose MetabolismInsulin SecretionIon ChannelsPancreatic Islets

Identifiers

PMID23788641
PMCPMC3743485
OpenAlexW2068642473

What Socratic 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 Socratic graph.