Evidence map›Paper›PMID 15998803›Full record

ArticleThe Journal of cell biology2005

Fc{epsilon}RI-mediated mast cell degranulation requires calcium-independent microtubule-dependent translocation of granules to the plasma membrane.

Keigo Nishida, Satoru Yamasaki, Yukitaka Ito, Koki Kabu, Kotaro Hattori, Tohru Tezuka, Hirofumi Nishizumi, Daisuke Kitamura, Ryo Goitsuka, Raif S Geha and 3 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 129 papers.

0numbers the graph read from it
0cells of the map it votes in
129citing papers in PubMed
4.4field-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

129 citing papers in PubMed, 309 citations in OpenAlex.

  1. A Review: Mast Cells as Targets for Glucocorticoid Action.Current allergy and asthma reports · 2026
    Review
  2. Article
  3. Review
  4. Article
  5. RIPK1 ubiquitination regulates its kinase-independent function in development and inflammation.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. LRO biogenesis and function: what can we learn from mast cells?Frontiers in cell and developmental biology · 2025
    Review
  14. Article
  15. Article
  16. Mast cell-sensory neuron crosstalk in allergic diseases.The Journal of allergy and clinical immunology · 2024
    Review
  17. Review
  18. Article
  19. Article
  20. Article

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

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

13 authors at 5 institutions in 2 countries.

Keigo NishidaLaboratory for Cytokine Signaling, RIKEN Research Center for Allergy and Immunology, Kanagawa 230-0045, Japan.
Satoru Yamasaki
Yukitaka Ito
Koki Kabu
Kotaro Hattori
Tohru Tezuka
Hirofumi Nishizumi
Daisuke Kitamura
Ryo Goitsuka
Raif S Geha
Tadashi Yamamoto
Takeshi Yagi
Toshio Hirano
RIKEN Center for Integrative Medical Sciences · JPOsaka University · JPTokyo University of Science · JPThe University of Tokyo · JPHarvard University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aggregation of high affinity IgE receptors (Fcepsilon receptor I [FcepsilonRI]) on mast cells is potent stimulus for the release of inflammatory and allergic mediators from cytoplasmic granules. However, the molecular mechanism of degranulation has not yet been established. It is still unclear how FcepsilonRI-mediated signal transduction ultimately regulates the reorganization of the cytoskeleton and how these events lead to degranulation. Here, we show that FcepsilonRI stimulation triggers the formation of microtubules in a manner independent of calcium. Drugs affecting microtubule dynamics effectively suppressed the FcepsilonRI-mediated translocation of granules to the plasma membrane and degranulation. Furthermore, the translocation of granules to the plasma membrane occurred in a calcium-independent manner, but the release of mediators and granule-plasma membrane fusion were completely dependent on calcium. Thus, the degranulation process can be dissected into two events: the calcium-independent microtubule-dependent translocation of granules to the plasma membrane and calcium-dependent membrane fusion and exocytosis. Finally, we show that the Fyn/Gab2/RhoA (but not Lyn/SLP-76) signaling pathway plays a critical role in the calcium-independent microtubule-dependent pathway.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCalciumCalcium SignalingCell DegranulationCell MembraneCells, CulturedExocytosisInflammation MediatorsMast CellsMembrane FusionMiceMice, Inbred C57BLMicrotubulesPhosphoproteinsProtein TransportAdaptor Proteins, Signal TransducingCalciumFyn protein, mouseGab2 protein, mouseInflammation MediatorsPhosphoproteinsProto-Oncogene ProteinsProto-Oncogene Proteins c-fynReceptors, IgErhoA GTP-Binding Proteinsrc-Family Kinases

Identifiers

PMID15998803
PMCPMC2171390
OpenAlexW2131929080

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.