Evidence map›Paper›PMID 19496745›Full record

ReviewCritical reviews in immunology2009

Regulation of Ca2+ signaling with particular focus on mast cells.

Hong-Tao Ma, Michael A Beaven

Open access · greenAbstract readReview
In one paragraph

Review in Critical reviews in immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

52 citing papers in PubMed, 139 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Ethanol Extract ofAdvances in pharmacological and pharmaceutical sciences · 2024
    Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Anti-Allergic and Anti-Inflammatory Effects of Neferine on RBL-2H3 Cells.International journal of molecular sciences · 2021
    Article
  10. The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2021
    Article
  11. Review
  12. Article
  13. Review
  14. TPC1 deficiency or blockade augments systemic anaphylaxis and mast cell activity.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  15. Analysis of Mrgprb2 Receptor-Evoked CaFrontiers in immunology · 2020
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

2 authors at 2 institutions in 1 country.

Hong-Tao MaLaboratory of Molecular Immunology, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA.
Michael A Beaven
National Heart Lung and Blood Institute · USNational Institutes of Health · US

Funding

Secretion Of Granules From Mast CellsZIAHL000993 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI BEAVEN, MICHAEL A · 2009 to 2010
$535k
Intramural NIH HHS ZIA HL000993
6 · The paper itself

Abstract

Calcium signals mediate diverse cellular functions in immunological cells. Early studies with mast cells, then a preeminent model for studying Ca2+-dependent exocytosis, revealed several basic features of calcium signaling in non-electrically excitable cells. Subsequent studies in these and other cells further defined the basic processes such as inositol 1,4,5-trisphosphate-mediated release of Ca2+ from Ca2+ stores in the endoplasmic reticulum (ER); coupling of ER store depletion to influx of external Ca2+ through a calcium-release activated calcium (CRAC) channel now attributed to the interaction of the ER Ca2+ sensor, stromal interacting molecule-1 (STIM1), with a unique Ca2+-channel protein, Orai1/CRACM1, and subsequent uptake of excess Ca2+ into ER and mitochondria through ATP-dependent Ca2+ pumps. In addition, transient receptor potential channels and ion exchangers also contribute to the generation of calcium signals that may be global or have dynamic (e.g., waves and oscillations) and spatial resolution for specific functional readouts. This review discusses past and recent developments in this field of research, the pharmacologic agents that have assisted in these endeavors, and the mast cell as an exemplar for sorting out how calcium signals may regulate multiple outputs in a single cell.

Indexed as

AnimalsCalciumCalcium ChannelsCalcium SignalingCalcium-Transporting ATPasesHumansInositol 1,4,5-Trisphosphate ReceptorsMast CellsMembrane PotentialsMembrane ProteinsMitochondriaSignal TransductionTRPC Cation ChannelsCalciumCalcium ChannelsCalcium-Transporting ATPasesInositol 1,4,5-Trisphosphate ReceptorsMembrane ProteinsTRPC Cation Channels

Identifiers

PMID19496745
PMCPMC2954050
OpenAlexW2053968716

What OpenQuestion holds

Textmetadata
LicenceTDM
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.