Evidence map›Paper›PMID 10066244›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience1999

Cloning and expression of a novel member of the low voltage-activated T-type calcium channel family.

J H Lee, A N Daud, L L Cribbs, A E Lacerda, A Pereverzev, U Klöckner, T Schneider, E Perez-Reyes

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 155 papers.

0numbers the graph read from it
0cells of the map it votes in
155citing papers in PubMed
–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

155 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Review
  4. Blockade of CaBritish journal of pharmacology · 2024
    Article
  5. Article
  6. The T-type calcium channelosome.Pflugers Archiv : European journal of physiology · 2024
    Review
  7. Article
  8. Review
  9. Review
  10. CaHandbook of experimental pharmacology · 2023
    Article
  11. Review
  12. Review
  13. Regulation of Presynaptic Calcium Channels.Advances in neurobiology · 2023
    Article
  14. Review
  15. T-Type Calcium Channels: A Mixed Blessing.International journal of molecular sciences · 2022
    Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

95 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

8 authors.

J H LeeDepartment of Physiology, Loyola University Medical Center, Maywood, Illinois 60153, USA.
A N Daud
L L Cribbs
A E Lacerda
A Pereverzev
U Klöckner
T Schneider
E Perez-Reyes

Funding

NHLBI NIH HHS HL57828
6 · The paper itself

Abstract

Low voltage-activated Ca2+ channels play important roles in pacing neuronal firing and producing network oscillations, such as those that occur during sleep and epilepsy. Here we describe the cloning and expression of the third member of the T-type family, alpha1I or CavT.3, from rat brain. Northern analysis indicated that it is predominantly expressed in brain. Expression of the cloned channel in either Xenopus oocytes or stably transfected human embryonic kidney-293 cells revealed novel gating properties. We compared these electrophysiological properties to those of the cloned T-type channels alpha1G and alpha1H and to the high voltage-activated channels formed by alpha1Ebeta3. The alpha1I channels opened after small depolarizations of the membrane similar to alpha1G and alpha1H but at more depolarized potentials. The kinetics of activation and inactivation were dramatically slower, which allows the channel to act as a Ca2+ injector. In oocytes, the kinetics were even slower, suggesting that components of the expression system modulate its gating properties. Steady-state inactivation occurred at higher potentials than any of the other T channels, endowing the channel with a substantial window current. The alpha1I channel could still be classified as T-type by virtue of its criss-crossing kinetics, its slow deactivation (tail current), and its small (11 pS) conductance in 110 mM Ba2+ solutions. Based on its brain distribution and novel gating properties, we suggest that alpha1I plays important roles in determining the electroresponsiveness of neurons, and hence, may be a novel drug target.

Indexed as

Cloning, MolecularAmino Acid SequenceAnimalsCalcium ChannelsCalcium Channels, T-TypeCell LineDNA, ComplementaryElectrophysiologyFemaleGene ExpressionHomeostasisHumansIon Channel GatingKineticsMolecular Sequence DataOocytesCalcium ChannelsCalcium Channels, T-TypeDNA, Complementary

Identifiers

PMID10066244
PMCPMC6782566

What OpenQuestion holds

Texttitle and abstract
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.