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Toll-like Receptor 1/2 Agonist Pam3CSK4 Suppresses Lipopolysaccharide-driven IgG1 Production while Enhancing IgG2a Production by B Cells
Immune Network ; : e10-2018.
Article Dans Anglais | WPRIM | ID: wpr-740202
ABSTRACT
Interaction between pathogen-associated molecular patterns and pattern recognition receptors triggers innate and adaptive immune responses. Several studies have reported that toll-like receptors (TLRs) are involved in B cell proliferation, differentiation, and Ig class switch recombination (CSR). However, roles of TLRs in B cell activation and differentiation are not completely understood. In this study, we investigated the direct effect of stimulation of TLR1/2 agonist Pam3CSK4 on mouse B cell viability, proliferation, activation, Ig production, and Ig CSR in vitro. Treatment with 0.5 µg/ml of Pam3CSK4 only barely induced IgG1 production although it enhanced B cell viability. In addition, high-dosage Pam3CSK4 diminished IgG1 production in a dose-dependent manner, whereas the production of other Igs, cell viability, and proliferation increased. Pam3CSK4 additively increased TLR4 agonist lipopolysaccharide (LPS)-induced mouse B cell growth and activation. However, interestingly, Pam3CSK4 abrogated LPS-induced IgG1 production but enhanced LPS-induced IgG2a production. Further, Pam3CSK4 decreased LPS-induced germline γ1 transcripts (GLTγ1)/GLTε expression but increased GLTγ2a expression. On the other hand, Pam3CSK4 had no effect on LPS-induced plasma cell differentiation. Taken together, these results suggest that TLR1/2 agonist Pam3CSK4 acts as a potent mouse B cell mitogen in combination with TLR4 agonist LPS, but these 2 different TLR agonists play diverse roles in regulating the Ig CSR of each isotype, particularly IgG1/IgE and IgG2a.
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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Plasmocytes / Recombinaison génétique / Techniques in vitro / Immunoglobuline E / Immunoglobuline G / Lymphocytes B / Survie cellulaire / Commutation de classe des immunoglobulines / Prolifération cellulaire / Récepteurs de reconnaissance de motifs moléculaires Limites du sujet: Animaux langue: Anglais Texte intégral: Immune Network Année: 2018 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Plasmocytes / Recombinaison génétique / Techniques in vitro / Immunoglobuline E / Immunoglobuline G / Lymphocytes B / Survie cellulaire / Commutation de classe des immunoglobulines / Prolifération cellulaire / Récepteurs de reconnaissance de motifs moléculaires Limites du sujet: Animaux langue: Anglais Texte intégral: Immune Network Année: 2018 Type: Article