Evidence map›Paper›PMID 26257741›Full record

ReviewFrontiers in immunology2015

Signature Channels of Excitability no More: L-Type Channels in Immune Cells.

Bennett Davenport, Yuan Li, Justin W Heizer, Carsten Schmitz, Anne-Laure Perraud

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

23 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. NaThe Journal of membrane biology · 2026
    Article
  3. Review
  4. TPC Functions in the Immune System.Handbook of experimental pharmacology · 2023
    Article
  5. CACNA1C-Related Channelopathies.Handbook of experimental pharmacology · 2023
    Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. CACNA1S haploinsufficiency confers resistance to New World arenavirus infection.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. L-Type Cav 1.2 Calcium Channel-α-1C Regulates Response to Rituximab in Diffuse Large B-Cell Lymphoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2019
    Article
  18. Review
  19. Review
  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

5 authors.

Bennett DavenportDepartment of Biomedical Research, National Jewish Health , Denver, CO , USA ; Department of Immunology and Microbiology, University of Colorado Denver , Denver, CO , USA.
Yuan LiDepartment of Biomedical Research, National Jewish Health , Denver, CO , USA ; Department of Immunology and Microbiology, University of Colorado Denver , Denver, CO , USA.
Justin W HeizerDepartment of Biomedical Research, National Jewish Health , Denver, CO , USA ; Department of Immunology and Microbiology, University of Colorado Denver , Denver, CO , USA.
Carsten SchmitzDepartment of Biomedical Research, National Jewish Health , Denver, CO , USA ; Department of Immunology and Microbiology, University of Colorado Denver , Denver, CO , USA.
Anne-Laure PerraudDepartment of Biomedical Research, National Jewish Health , Denver, CO , USA ; Department of Immunology and Microbiology, University of Colorado Denver , Denver, CO , USA.

Funding

Structure-function relationships of the chimeric TRPM7 channel-kinaseR01GM090123 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI SCHMITZ, CARSTEN · 2010 to 2014
$1.4M
Function of L-Type Ca2+ Channels in B-LymphocytesR21AI078400 · NIAID · NATIONAL JEWISH HEALTH · PI PERRAUD, ANNE-LAURE · 2008 to 2009
$429k
NIAID NIH HHS R21 AI078400NIGMS NIH HHS R01 GM090123
6 · The paper itself

Abstract

Although the concept of Ca(2+) as a universal messenger is well established, it was assumed that the regulatory mechanisms of Ca(2+)-signaling were divided along the line of electric excitability. Recent advances in molecular biology and genomics have, however, provided evidence that non-excitable cells such as immunocytes also express a wide and diverse pool of ion channels that does not differ as significantly from that of excitable cells as originally assumed. Ion channels and transporters are involved in virtually all aspects of immune response regulation, from cell differentiation and development to activation, and effector functions such as migration, antibody-secretion, phagosomal maturation, or vesicular delivery of bactericidal agents. This comprises TRP channel family members, voltage- and Ca(2+)-gated K(+)- and Na(+)-channels, as well as unexpectedly, components of the CaV1-subfamily of voltage-gated L-type Ca(2+)-channels, originally thought to be signature molecules of excitability. This article provides an overview of recent observations made in the field of CaV1 L-type channel function in the immune context, as well as presents results we obtained studying these channels in B-lymphocytes.

Indexed as

calcium signalingCaV ion channelsdihydropyridinesDT40 B-cellsL-type channelslymphocytesmyeloid lineage

Identifiers

PMID26257741
PMCPMC4512153

What OpenQuestion holds

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Registered trials

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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.