Phosphoproteomic analyses reveal that galectin-1 augments the dynamics of B-cell receptor signaling

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Title:	Phosphoproteomic analyses reveal that galectin-1 augments the dynamics of B-cell receptor signaling
Authors:	吳忻怡;Tsai, Chih-Ming;Wu, Hsin-Yi;Su, Tseng-Hsiung;Kuo, Chu-Wei;Huang, Han-Wen;Chung, Cheng-Han;Chen, Chien-Sin;Khoo, Kay-Hooi;Chen, Yu-Ju;Lin, Kuo-I
Contributors:	總教學中心通識教育中心
Keywords:	animal models;Animals;Antibodies, Anti-Idiotypic - pharmacology;antibody formation;antigens;B-cell activation;B-cell receptor;B-lymphocytes;B-Lymphocytes - physiology;Galectin 1 - deficiency;Galectin 1 - physiology;Galectin-1;humoral immunity;immunological synapse;Lymphocyte Activation - drug effects;Mice, Inbred C57BL;phosphatidylinositol 3-kinase;Phosphatidylinositol 3-Kinases - metabolism;phosphoproteins;Phosphoproteins - isolation & purification;Phosphoproteome;phosphorylation;proteomics;Proteomics - methods;Receptors, Antigen, B-Cell - physiology;Signal Transduction;Western blotting
Date:	2014-05-30
Issue Date:	2026-04-23 12:54:59 (UTC+8)
Publisher:	Elsevier;Netherlands: Elsevier B.V
Abstract:	摘要： B-cell activation is important for mounting humoral immune responses and antibody production. Galectin-1 has multiple regulatory functions in immune cells. However, the effects of galectin-1 modulation and the mechanisms underlying the coordination of B-cell activation are unclear. To address this issue, we applied label-free quantitative phosphoproteomic analysis to investigate the dynamics of galectin-1-induced signaling in comparison with that following anti-IgM treatment. A total of 3247 phosphorylation sites on 1245 proteins were quantified, and 70–80% of the 856 responsive phosphoproteins were commonly activated during various biological functions. The similarity between galectin-1- and anti-IgM-elicited B-cell receptor (BCR) signaling pathways was also revealed. Additionally, the mapping of the 149 BCR-responsive phosphorylation sites provided complementary knowledge of BCR signaling. Compared to anti-IgM induction, the phosphoproteomic profiling of BCR signaling, along with validation by western blot analysis and pharmacological inhibitors, revealed that the activation of Syk, Btk, and PI3K may be dominant in galectin-1-mediated activation. We further demonstrated that the proliferation of antigen-primed B cells was diminished in the absence of galectin-1 in an animal model. Together, these findings provided evidence for a new role and insight into the mechanism of how galectin-1 augments the strength of the immunological synapse by modulating BCR signaling. The current study revealed the first systematic phosphorylation-mediated signaling network and its dynamics in B cell activation. The comparative phosphoproteomic analysis on the dynamics of galectin-1 induced activation profiles not only showed that exogenously added galectin-1 augmented B-cell activation but also revealed its relatively enhanced activation in PI3K pathway. Together with proliferation assay, we further delineated that galectin-1 is important for B-cell proliferation in response to antigen challenge. Our phosphoproteomic study reveals a new role for galectin-1 in augmenting the strength of immunological synapse by modulating BCR signaling. [Display omitted] •First systematic analysis on the dynamic phosphoproteome of B cell activation.•Phosphoproteomics revealed similarity between galectin-1- and anti-IgM-elicited signaling.•PI3K pathway is more enhanced in the rGal-1-mediated B cell activation.•Galectin-1 is important for B-cell proliferation in response to antigen challenge. 其他題名： J Proteomics 出版者： Netherlands: Elsevier B.V 出版日期： 2014-05-30 出處： Journal of proteomics, 2014-05, Vol.103, p.241-253 版權： 2014 Elsevier B.V. 版權： Copyright © 2014 Elsevier B.V. All rights reserved. 識別號： ISSN: 1874-3919 識別號： ISSN: 1876-7737 識別號： EISSN: 1876-7737 識別號： DOI: 10.1016/j.jprot.2014.03.031 識別號： PMID: 24704852
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