Monomer hapten and hapten-specific IgG inhibit mast cell activation evoked by multivalent hapten with different mechanisms.


Journal

European journal of immunology
ISSN: 1521-4141
Titre abrégé: Eur J Immunol
Pays: Germany
ID NLM: 1273201

Informations de publication

Date de publication:
12 2019
Historique:
received: 16 10 2018
revised: 19 06 2019
accepted: 19 07 2019
pubmed: 25 7 2019
medline: 28 5 2020
entrez: 25 7 2019
Statut: ppublish

Résumé

Aggregation of IgE bound to high affinity IgE receptor (FcεRI) by multivalent antigen induces mast cell activation. Reportedly, disaggregation of aggregated FcεRI immediately terminated degranulation, and formation of co-ligated FcεRI and low affinity IgG receptor FcγRIIB blocked degranulation by inhibitory signal via SH2-containing inositol 5'-phosphatase 1 (SHIP1) phosphorylation. However, their molecular mechanisms to inhibit mast cell activation have been unclear in detail. Herein, we found that addition of excess monomeric hapten (TNP-alanine) to multivalent antigen (TNP-OVA)-activated rat basophilic leukemia cells and mouse bone marrow-derived mast cells induced immediate and transient Syk dephosphorylation, which was previously phosphorylated by TNP-OVA addition. Syk dephosphorylation correlated to rapidly decreased intracellular Ca

Identifiants

pubmed: 31339552
doi: 10.1002/eji.201847973
doi:

Substances chimiques

Antibodies, Monoclonal, Murine-Derived 0
Fcgr2b protein, mouse 0
Fcgr2b protein, rat 0
Haptens 0
Immunoglobulin G 0
Receptors, IgE 0
Receptors, IgG 0
Inpp5d protein, mouse EC 3.1.3.86
Phosphatidylinositol-3,4,5-Trisphosphate 5-Phosphatases EC 3.1.3.86

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2172-2183

Informations de copyright

© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Références

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Auteurs

Ruriko Suzuki (R)

Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya, Japan.

Yoshikazu Inoh (Y)

School of Pharmacy, Aichi Gakuin University, Nagoya, Japan.

Satoru Yokawa (S)

School of Pharmacy, Aichi Gakuin University, Nagoya, Japan.

Ryo Suzuki (R)

Faculty of Pharmaceutical Sciences, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Kanazawa, Japan.

Tadahide Furuno (T)

School of Pharmacy, Aichi Gakuin University, Nagoya, Japan.

Naohide Hirashima (N)

Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya, Japan.

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