Evidence map›Paper›PMID 27037192›Full record

ArticleImmunity2016

Low-Voltage-Activated CaV3.1 Calcium Channels Shape T Helper Cell Cytokine Profiles.

Huiyun Wang, Xuexin Zhang, Li Xue, Juan Xing, Marie-Hélène Jouvin, James W Putney, Matthew P Anderson, Mohamed Trebak, Jean-Pierre Kinet

Open access · bronzeAbstract read
In one paragraph

Article in Immunity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 52 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. The T-type calcium channelosome.Pflugers Archiv : European journal of physiology · 2024
    Review
  9. Article
  10. Review
  11. TPC Functions in the Immune System.Handbook of experimental pharmacology · 2023
    Article
  12. Dual near-infrared II laser modulates the cellular redox state of T cells and augments the efficacy of cancer immunotherapy.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  13. CaJournal of thrombosis and haemostasis : JTH · 2022
    Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Altered CaInternational journal of molecular sciences · 2020
    Review
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  20. Article
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 5 institutions in 1 country.

Huiyun WangDepartment of Pathology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA 02115, USA.
Xuexin ZhangDepartment of Cellular and Molecular Physiology, Penn State University College of Medicine, Hershey, PA 17033, USA.
Li XueDepartment of Pathology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA 02115, USA.
Juan XingLaboratory of Signal Transduction, NIEHS, National Institutes of Health, Research Triangle Park, NC 27709, USA.
Marie-Hélène JouvinDepartment of Pathology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA 02115, USA.
James W PutneyLaboratory of Signal Transduction, NIEHS, National Institutes of Health, Research Triangle Park, NC 27709, USA.
Matthew P AndersonDepartment of Pathology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA 02115, USA; Department of Neurology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA 02115, USA.
Mohamed TrebakDepartment of Cellular and Molecular Physiology, Penn State University College of Medicine, Hershey, PA 17033, USA.
Jean-Pierre KinetDepartment of Pathology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA 02115, USA. Electronic address: jkinet2@me.com.
Harvard University · USBeth Israel Deaconess Medical Center · USPennsylvania State University · USNational Institute of Environmental Health Sciences · USNational Institutes of Health · US

Funding

Molecular analysis of FCERI signaling and functionR37GM053950 · NIGMS · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KINET, JEAN-PIERRE M · 2004 to 2013
$4.2M
Receptor-regulated Ca2+ Entry Pathways in Smooth MuscleR01HL097111 · NHLBI · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI TREBAK, MOHAMED · 2010 to 2019
$3.7M
Neurobiological Mechanism of 15q11-13 Duplication Autism Spectrum DisorderR01NS081916 · NINDS · BETH ISRAEL DEACONESS MEDICAL CENTER · PI ANDERSON, MATTHEW P · 2012 to 2016
$1.9M
Characterization of new Ca2+ channels that underpin immunological decision makingR01AI095308 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KINET, JEAN-PIERRE M · 2012 to 2015
$1.7M
Leukotriene C4 and STIM/Orai channels in airway smooth muscle remodelingR01HL123364 · NHLBI · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI TREBAK, MOHAMED · 2014 to 2017
$1.5M
NHLBI NIH HHS 5T32HL789315NHLBI NIH HHS HL097111NHLBI NIH HHS R01 HL097111NHLBI NIH HHS R01 HL123364NIAID NIH HHS 1R01AI095308NIAID NIH HHS R01 AI095308NIGMS NIH HHS 5R37GM53950NIGMS NIH HHS R37 GM053950NINDS NIH HHS 5R01NS081916NINDS NIH HHS R01 NS081916
6 · The paper itself

Abstract

Activation of T cells is mediated by the engagement of T cell receptors (TCRs) followed by calcium entry via store-operated calcium channels. Here we have shown an additional route for calcium entry into T cells-through the low-voltage-activated T-type CaV3.1 calcium channel. CaV3.1 mediated a substantial current at resting membrane potentials, and its deficiency had no effect on TCR-initiated calcium entry. Mice deficient for CaV3.1 were resistant to the induction of experimental autoimmune encephalomyelitis and had reduced productions of the granulocyte-macrophage colony-stimulating factor (GM-CSF) by central nervous system (CNS)-infiltrating T helper 1 (Th1) and Th17 cells. CaV3.1 deficiency led to decreased secretion of GM-CSF from in vitro polarized Th1 and Th17 cells. Nuclear translocation of the nuclear factor of activated T cell (NFAT) was also reduced in CaV3.1-deficient T cells. These data provide evidence for T-type channels in immune cells and their potential role in shaping the autoimmune response.

Indexed as

Active Transport, Cell NucleusAnimalsAutoimmunityCalciumCalcium Channels, T-TypeCytokinesEncephalomyelitis, Autoimmune, ExperimentalFemaleGranulocyte-Macrophage Colony-Stimulating FactorLymphocyte ActivationMiceMice, Inbred C57BLMice, KnockoutNFATC Transcription FactorsTh17 CellsTh1 CellsCacna1g protein, mouseCalciumCalcium Channels, T-TypeCytokinesGranulocyte-Macrophage Colony-Stimulating FactorNFATC Transcription Factors

Identifiers

PMID27037192
PMCPMC6771933
OpenAlexW2325899309

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.