Evidence map›Paper›PMID 19332490›Full record

ArticleThe Journal of physiology2009

TRPC1 and STIM1 mediate capacitative Ca2+ entry in mouse pulmonary arterial smooth muscle cells.

Lih Chyuan Ng, Mary D McCormack, Judith A Airey, Cherie A Singer, Phillip S Keller, Xiao-Ming Shen, Joseph R Hume

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

51 citing papers in PubMed, 94 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Notch enhances CaAmerican journal of physiology. Cell physiology · 2020
    Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Store depletion induces Gαq-mediated PLCβ1 activity to stimulate TRPC1 channels in vascular smooth muscle cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2016
    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

7 authors at 1 institution in 1 country.

Lih Chyuan NgDepartment of Pharmacology, University of Nevada School of Medicine, Reno, NV 89557, USA. lcng@medicine.nevada.edu
Mary D McCormack
Judith A Airey
Cherie A Singer
Phillip S Keller
Xiao-Ming Shen
Joseph R Hume
University of Nevada, Reno · US

Funding

Signal transduction pathways regulated by cell volumeP20RR015581 · NCRR · UNIVERSITY OF NEVADA RENO · PI BRITTON, FIONA CATHERINE · 2000 to 2009
$19.5M
IONIC AND PHARMACOLOGICAL REGULATION OF VASCULAR CELLSR37HL049254 · NHLBI · UNIVERSITY OF NEVADA RENO · PI HUME, JOSEPH R · 1998 to 2007
$2.7M
IONIC AND PHARMACOLOGICAL REGULATION OF VASCULAR CELLSR01HL049254 · NHLBI · UNIVERSITY OF NEVADA RENO · PI HUME, JOSEPH R · 1993 to 1998
–
NCRR NIH HHS P20 RR015581NCRR NIH HHS P20RR15581NHLBI NIH HHS HL 49254NHLBI NIH HHS R01 HL049254NHLBI NIH HHS R37 HL049254
6 · The paper itself

Abstract

Previous studies in pulmonary arterial smooth muscle cells (PASMCs) showed that the TRPC1 channel mediates capacitative Ca(2+) entry (CCE), but the molecular signal(s) that activate TRPC1 in PASMCs remains unknown. The aim of the present study was to determine if TRPC1 mediates CCE through activation of STIM1 protein in mouse PASMCs. In primary cultured mouse PASMCs loaded with fura-2, cyclopiazonic acid (CPA) caused a transient followed by a sustained rise in intracellular Ca(2+) concentration ([Ca(2+)](i)). The transient but not the sustained rise in [Ca(2+)](i) was partially inhibited by nifedipine. In addition, CPA increased the rate of Mn(2+) quench of fura-2 fluorescence that was inhibited by SKF 96365, Ni(2+), La(3+) and Gd(3+), exhibiting pharmacological properties characteristic of CCE. The nifedipine-insensitive sustained rise in [Ca(2+)](i) and the increase in Mn(2+) quench of fura-2 fluorescence caused by CPA were both inhibited in cells pretreated with antibody raised against an extracellular epitope of TRPC1. Moreover, STIM1 siRNA reduced the rise in [Ca(2+)](i) and Mn(2+) quench of fura-2 fluorescence caused by CPA, whereas overexpression of STIM1 resulted in a marked increase in these responses. RT-PCR revealed TRPC1 and STIM1 mRNAs, and Western blot analysis identified TRPC1 and STIM1 proteins in mouse PASMCs. Furthermore, TRPC1 was found to co-immunoprecipitate with STIM1, and the precipitation level of TRPC1 was increased in cells subjected to store depletion. Taken together, store depletion causes activation of voltage-operated Ca(2+) entry and CCE. These data provide direct evidence that CCE is mediated by TRPC1 channel through activation of STIM1 in mouse PASMCs.

Indexed as

Calcium SignalingAminoquinolinesAnimalsCalcium Channel BlockersCalcium ChannelsCalcium-Transporting ATPasesCells, CulturedEnzyme InhibitorsGadoliniumIndolesLanthanumMagnesiumMaleMembrane GlycoproteinsMembrane PotentialsMice1-(2-methylphenyl)-4-methylamino-6-methyl-2,3-dihydropyrrolo(3,2-c)quinolineAminoquinolinesCalcium Channel BlockersCalcium ChannelsCalcium-Transporting ATPasescyclopiazonic acidEnzyme InhibitorsGadoliniumIndolesLanthanumMagnesiumMembrane GlycoproteinsNickelNifedipineRNA, MessengerStim1 protein, mouseStromal Interaction Molecule 1transient receptor potential cation channel, subfamily C, member 1TRPC Cation Channels

Identifiers

PMID19332490
PMCPMC2714011
OpenAlexW1513858292

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.