Evidence map›Paper›PMID 16272347›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2005

Positive and negative regulation of mast cell activation by Lyn via the FcepsilonRI.

Wenbin Xiao, Hajime Nishimoto, Hong Hong, Jiro Kitaura, Satoshi Nunomura, Mari Maeda-Yamamoto, Yuko Kawakami, Clifford A Lowell, Chisei Ra, Toshiaki Kawakami

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

72 citing papers in PubMed, 158 citations in OpenAlex.

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  18. Article
  19. Mechanisms of Allergen Immunotherapy in Allergic Rhinitis.Current allergy and asthma reports · 2020
    Review
  20. Strategies for Mast Cell Inhibition in Food Allergy.The Yale journal of biology and medicine · 2020
    Review

12 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

10 authors at 4 institutions in 2 countries.

Wenbin XiaoDivision of Cell Biology, La Jolla Institute for Allergy and Immunology, San Diego, CA 92121, USA.
Hajime Nishimoto
Hong Hong
Jiro Kitaura
Satoshi Nunomura
Mari Maeda-Yamamoto
Yuko Kawakami
Clifford A Lowell
Chisei Ra
Toshiaki Kawakami
La Jolla Institute for Immunology · USNihon University · JPNational Agriculture and Food Research Organization · JPUniversity of California, San Francisco · US

Funding

IgE Regulation of Mast Cell Growth and SurvivalR01AI050209 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI KAWAKAMI, TOSHIAKI · 2002 to 2006
$2.3M
ROLES OF PH DOMAINS IN MAST CELL SIGNAL TRANSDUCTIONR01AI038348 · NIAID · LA JOLLA INST FOR ALLERGY &IMMUNOLGY · PI KAWAKAMI, TOSHIAKI · 1996 to 2005
$1.3M
NIAID NIH HHS R01 AI038348NIAID NIH HHS R01 AI050209
6 · The paper itself

Abstract

Aggregation of the high affinity receptor for IgE (FcepsilonRI) induces activation of mast cells. In this study we show that upon low intensity stimulation of FcepsilonRI with monomeric IgE, IgE plus anti-IgE, or IgE plus low Ag, Lyn (a Src family kinase) positively regulates degranulation, cytokine production, and survival, whereas Lyn works as a negative regulator of high intensity stimulation with IgE plus high Ag. Low intensity stimulation suppressed Lyn kinase activity and its association with FcepsilonRI beta subunit, whereas high intensity stimulation enhanced Lyn activity and its association with FcepsilonRI beta. The latter induced much higher levels of FcepsilonRI beta phosphorylation and Syk activity than the former. Downstream positive signaling molecules, such as Akt and p38, were positively and negatively regulated by Lyn upon low and high intensity stimulations, respectively. In contrast, the negative regulators, SHIP and Src homology 2 domain-containing protein tyrosine phosphatase-1, interacted with FcepsilonRI beta, and their phosphorylation was controlled by Lyn. Therefore, we conclude that Lyn-mediated positive vs negative regulation depends on the intensity of the stimuli. Studies of mutant FcepsilonRI beta showed that FcepsilonRI beta subunit-ITAM (ITAM motif) regulates degranulation and cytokine production positively and negatively depending on the intensity of FcepsilonRI stimulation. Furthermore, Lyn-mediated negative regulation was shown to be exerted via the FcepsilonRI beta-ITAM.

Indexed as

AnimalsAntigensCell DegranulationCells, CulturedCell SurvivalCytokinesImmunoglobulin EIntracellular Signaling Peptides and ProteinsMast CellsMiceMice, Knockoutp38 Mitogen-Activated Protein KinasesPhosphatidylinositol-3,4,5-Trisphosphate 5-PhosphatasesPhosphoric Monoester HydrolasesPhosphorylationProtein Phosphatase 1AntigensCytokinesImmunoglobulin EINPPL1 protein, humanIntracellular Signaling Peptides and Proteinslyn protein-tyrosine kinasep38 Mitogen-Activated Protein KinasesPhosphatidylinositol-3,4,5-Trisphosphate 5-PhosphatasesPhosphoric Monoester HydrolasesProtein Phosphatase 1Protein Tyrosine Phosphatase, Non-Receptor Type 6Protein Tyrosine PhosphatasesProto-Oncogene Proteins c-aktPTPN6 protein, humanPtpn6 protein, mouseReceptors, IgEsrc-Family Kinases

Identifiers

PMID16272347
PMCPMC1415265
OpenAlexW2168921529

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.