Evidence map›Paper›PMID 9449328›Full record

ArticleBiophysical journal1998

Inactivating BK channels in rat chromaffin cells may arise from heteromultimeric assembly of distinct inactivation-competent and noninactivating subunits.

J P Ding, Z W Li, C J Lingle

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
1.9field-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

45 citing papers in PubMed, 78 citations in OpenAlex.

  1. Article
  2. Article
  3. Calcium-Activated KHandbook of experimental pharmacology · 2021
    Article
  4. LINGO1 is a regulatory subunit of large conductance, CaProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Roles of NaPflugers Archiv : European journal of physiology · 2018
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Functional regulation of BK potassium channels by γ1 auxiliary subunits.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  19. Review
  20. Review
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

3 authors at 1 institution in 1 country.

J P DingDepartment of Anesthesiology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Z W Li
C J Lingle
Washington University in St. Louis · US

Funding

CALCIUM-ACTIVATED POTASSIUM CHANNELSR01DK046564 · NIDDK · WASHINGTON UNIVERSITY · PI LINGLE, CHRISTOPHER J · 1993 to 2006
$1.8M
NIDDK NIH HHS DK-46564
6 · The paper itself

Abstract

Inactivating and noninactivating variants of large-conductance, Ca2+-dependent, voltage-dependent BK-type channels are found in rat chromaffin cells and are largely segregated into different cells. Here we test the hypothesis that, within the population of cells that express inactivating BK current (BKi current), the BKi channels are largely heteromultimers composed of inactivation-competent subunits (bk(i)) and noninactivating subunits (bk(s)). Several independent types of evidence support this view. The gradual removal of inactivation by trypsin is consistent with the idea that in most cells and patches there are, on average, about two to three inactivation domains per channel. In addition, several aspects of blockade of BKi current by charybdotoxin (CTX) are consistent with the idea that BKi channels contain differing numbers (one to four) of relatively CTX-resistant bk(i) subunits. Finally, the frequency of occurrence of noninactivating BKs channels in patches with predominantly inactivating BKi channels is consistent with the binomial expectations of random, independent assembly of two distinct subunits, if most cells have, on average, about two to three bk(i) subunits per channel. These results suggest that the phenotypic properties of BKi currents and the resulting cellular electrical excitability may exhibit a continuum of behavior that arises simply from the differential expression of two distinct subunits.

Indexed as

Potassium Channels, Calcium-ActivatedAnimalsCell MembraneCells, CulturedCharybdotoxinChromaffin CellsCytosolGenetic VariationLarge-Conductance Calcium-Activated Potassium ChannelsMacromolecular SubstancesMembrane PotentialsModels, BiologicalModels, ChemicalPatch-Clamp TechniquesPhenotypePotassium ChannelsCharybdotoxinLarge-Conductance Calcium-Activated Potassium ChannelsMacromolecular SubstancesPotassium ChannelsPotassium Channels, Calcium-ActivatedTrypsin

Identifiers

PMID9449328
PMCPMC1299380
OpenAlexW1978257737

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.