Evidence map›Paper›PMID 17158339›Full record

ArticleCirculation research2007

Ca2+-dependent rapid Ca2+ sensitization of contraction in arterial smooth muscle.

George J Dimopoulos, Shingo Semba, Kazuyo Kitazawa, Masumi Eto, Toshio Kitazawa

Open access · bronzeAbstract read
In one paragraph

Article in Circulation research, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

76 citing papers in PubMed, 142 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Review
  6. Regulation of myosin light-chain phosphorylation and its roles in cardiovascular physiology and pathophysiology.Hypertension research : official journal of the Japanese Society of Hypertension · 2022
    Review
  7. Dynamic cytosolic CaAmerican journal of physiology. Lung cellular and molecular physiology · 2021
    Article
  8. Article
  9. Effects of TNFα on Dynamic Cytosolic CaFrontiers in physiology · 2021
    Article
  10. Review
  11. Article
  12. Article
  13. Implications of immune-inflammatory responses in smooth muscle dysfunction and disease.Journal of smooth muscle research = Nihon Heikatsukin Gakkai kikanshi · 2019
    Article
  14. Involvement of inhibitor kappa B kinase 2 (IKK2) in the regulation of vascular tone.Laboratory investigation; a journal of technical methods and pathology · 2018
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

George J DimopoulosBoston Biomedical Research Institute, 64 Grove St, Watertown, MA 02472, USA.
Shingo Semba
Kazuyo Kitazawa
Masumi Eto
Toshio Kitazawa
Boston Biomedical Research Institute · US

Funding

X-ray Crystallographic Investigation of Smooth Muscle RegulationP01AR041637 · NIAMS · BOSTON BIOMEDICAL RESEARCH INSTITUTE · PI TAO, TERENCE · 1992 to 2007
$15.1M
Mechanism of Ca2+ Sensitization in Smooth MuscleR01HL070881 · NHLBI · BOSTON BIOMEDICAL RESEARCH INSTITUTE · PI KITAZAWA, TOSHIO · 2002 to 2006
$2.9M
Regulation Vascular Smooth Muscle Myosin PhosphataseR01HL083261 · NHLBI · THOMAS JEFFERSON UNIVERSITY · PI ETO, MASUMI · 2006 to 2010
$1.3M
NHLBI NIH HHS R01 HL070881NHLBI NIH HHS R01 HL083261NHLBI NIH HHS R01HL083261NHLBI NIH HHS R01HL70881NIAMS NIH HHS P01 AR041637NIAMS NIH HHS P01AR041637
6 · The paper itself

Abstract

Ca(2+) ion is a universal intracellular messenger that regulates numerous biological functions. In smooth muscle, Ca(2+) with calmodulin activates myosin light chain (MLC) kinase to initiate a rapid MLC phosphorylation and contraction. To test the hypothesis that regulation of MLC phosphatase is involved in the rapid development of MLC phosphorylation and contraction during Ca(2+) transient, we compared Ca(2+) signal, MLC phosphorylation, and 2 modes of inhibition of MLC phosphatase, phosphorylation of CPI-17 Thr38 and MYPT1 Thr853, during alpha(1) agonist-induced contraction with/without various inhibitors in intact rabbit femoral artery. Phenylephrine rapidly induced CPI-17 phosphorylation from a negligible amount to a peak value of 0.38+/-0.04 mol of Pi/mol within 7 seconds following stimulation, similar to the rapid time course of Ca(2+) rise and MLC phosphorylation. This rapid CPI-17 phosphorylation was dramatically inhibited by either blocking Ca(2+) release from the sarcoplasmic reticulum or by pretreatment with protein kinase C inhibitors, suggesting an involvement of Ca(2+)-dependent protein kinase C. This was followed by a slow Ca(2+)-independent and Rho-kinase/protein kinase C-dependent phosphorylation of CPI-17. In contrast, MYPT1 phosphorylation had only a slow component that increased from 0.29+/-0.09 at rest to the peak of 0.68+/-0.14 mol of Pi/mol at 1 minute, similar to the time course of contraction. Thus, there are 2 components of the Ca(2+) sensitization through inhibition of MLC phosphatase. Our results support the hypothesis that the initial rapid Ca(2+) rise induces a rapid inhibition of MLC phosphatase coincident with the Ca(2+)-induced MLC kinase activation to synergistically initiate a rapid MLC phosphorylation and contraction in arteries with abundant CPI-17 content.

Indexed as

Adrenergic alpha-AgonistsAnimalsCalciumCalcium Channel BlockersCalcium SignalingFemoral ArteryIntracellular Signaling Peptides and ProteinsIn Vitro TechniquesMuscle ProteinsMuscle, Smooth, VascularMyosin-Light-Chain PhosphataseMyosin Light ChainsPhenylephrinePhosphoprotein PhosphatasesPhosphoproteinsPhosphorylationAdrenergic alpha-AgonistsCalciumCalcium Channel BlockersCPI-17 protein, Oryctolagus cuniculusIntracellular Signaling Peptides and ProteinsMuscle ProteinsMyosin-Light-Chain PhosphataseMyosin Light ChainsPhenylephrinePhosphoprotein PhosphatasesPhosphoproteinsProtein Kinase CProtein Kinase InhibitorsProtein Serine-Threonine KinasesProtein Subunitsrho-Associated KinasesVasoconstrictor Agents

Identifiers

PMID17158339
PMCPMC2212616
OpenAlexW2145953966

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.