Evidence map›Paper›PMID 12042350›Full record

ArticleThe Journal of physiology2002

Novel functional properties of Ca(2+) channel beta subunits revealed by their expression in adult rat heart cells.

Henry M Colecraft, Badr Alseikhan, Shoji X Takahashi, Dipayan Chaudhuri, Scott Mittman, Vasan Yegnasubramanian, Rebecca S Alvania, David C Johns, Eduardo Marbán, David T Yue

Abstract read
In one paragraph

Article in The Journal of physiology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 126 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
126citing 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

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

  1. Calcium and arrhythmogenesis.Physiological reviews · 2007
    Pooled it
  2. Review
  3. C-Terminus of CaCells · 2026
    Article
  4. Article
  5. Review
  6. Article
  7. 14-3-3 promotes sarcolemmal expression of cardiac CaProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Acute phosphatidylinositol 4,5 bisphosphate depletion destabilizes sarcolemmal expression of cardiac L-type CaProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. The βFrontiers in cardiovascular medicine · 2021
    Article
  19. Article
  20. Article

66 more citing papers are in PubMed but not listed here.

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

10 authors.

Henry M ColecraftProgram in Molecular and Cellular Systems Physiology, Department of Biomedical Engineering, Johns Hopkins University School of Medicine, Traylor Building, Room 710A, 720 Rutland Avenue, Baltimore, MD 21205, USA. hcolecra@bme.jhu.edu
Badr Alseikhan
Shoji X Takahashi
Dipayan Chaudhuri
Scott Mittman
Vasan Yegnasubramanian
Rebecca S Alvania
David C Johns
Eduardo Marbán
David T Yue

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recombinant adenoviruses were used to overexpress green fluorescent protein (GFP)-fused auxiliary Ca(2+) channel beta subunits (beta(1)-beta(4)) in cultured adult rat heart cells, to explore new dimensions of beta subunit functions in vivo. Distinct beta-GFP subunits distributed differentially between the surface sarcolemma, transverse elements, and nucleus in single heart cells. All beta-GFP subunits increased the native cardiac whole-cell L-type Ca(2+) channel current density, but produced distinctive effects on channel inactivation kinetics. The degree of enhancement of whole-cell current density was non-uniform between beta subunits, with a rank order of potency beta(2a) approximately equal to beta(4) > beta(1b) > beta(3). For each beta subunit, the increase in L-type current density was accompanied by a correlative increase in the maximal gating charge (Q(max)) moved with depolarization. However, beta subunits produced characteristic effects on single L-type channel gating, resulting in divergent effects on channel open probability (P(o)). Quantitative analysis and modelling of single-channel data provided a kinetic signature for each channel type. Spurred on by ambiguities regarding the molecular identity of the actual endogenous cardiac L-type channel beta subunit, we cloned a new rat beta(2) splice variant, beta(2b), from heart using 5' rapid amplification of cDNA ends (RACE) PCR. By contrast with beta(2a), expression of beta(2b) in heart cells yielded channels with a microscopic gating signature virtually identical to that of native unmodified channels. Our results provide novel insights into beta subunit functions that are unattainable in traditional heterologous expression studies, and also provide new perspectives on the molecular identity of the beta subunit component of cardiac L-type Ca(2+) channels. Overall, the work establishes a powerful experimental paradigm to explore novel functions of ion channel subunits in their native environments.

Indexed as

AdenoviridaeAnimalsBlotting, WesternCalcium ChannelsCalcium Channels, L-TypeDNA PrimersElectrophysiologyGenetic VectorsIon Channel GatingMembrane PotentialsModels, NeurologicalMyocardiumPatch-Clamp TechniquesPlasmidsRatsRecombinant ProteinsCacnb3 protein, ratCacnb4 protein, ratCalcium ChannelsCalcium Channels, L-TypeDNA PrimersRecombinant Proteins

Identifiers

PMID12042350
PMCPMC2290333

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.