Cited by 138Protein Kinase Regulation and GTPase SignalingT-cell and B-cell ImmunologyImmunodeficiency and Autoimmune Disorders

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Four Tyrosine Residues in Phospholipase C-γ2, Identified as Btk-dependent Phosphorylation Sites, Are Required for B Cell Antigen Receptor-coupled Calcium Signaling

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Watanabe, Dai, Hashimoto, Shoji, Ishiai, Masamichi, Matsushita, Masato, Baba, Yoshihiro, Kishimoto, Tadamitsu, Kurosaki, Tomohiro, Tsukada, Satoshi·2001·Journal of Biological Chemistry

DOI 10.1074/jbc.m103675200

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Abstract

Activation of phospholipase C-gamma2 (PLCgamma2) is the critical step in B cell antigen receptor (BCR)-coupled calcium signaling. Although genetic dissection experiments on B cells have demonstrated that Bruton's tyrosine kinase (Btk) and Syk are required for activating PLCgamma2, the exact activation mechanism of PLCgamma2 by these kinases has not been established. We identify the tyrosine residues 753, 759, 1197, and 1217 in rat PLCgamma2 as Btk-dependent phosphorylation sites by using an in vitro kinase assay. To evaluate the role of these tyrosine residues in phosphorylation-dependent activation of PLCgamma2, PLCgamma2-deficient DT40 cells were reconstituted with a series of mutant PLCgamma2s in which the phenylalanine was substituted for tyrosine. Substitution of all four tyrosine residues almost completely eliminated the BCR-induced PLCgamma2 phosphorylation, indicating that these residues include the major phosphorylation sites upon BCR engagement. Cells expressing PLCgamma2 with a single substitution exhibited some extent of reduction in calcium mobilization, whereas those expressing quadruple mutant PLCgamma2 showed greatly reduced calcium response. These findings indicate that the phosphorylations of the tyrosine residues 753, 759, 1197, and 1217, which have been identified as Btk-dependent phosphorylation sites in vitro, coordinately contribute to BCR-induced activation of PLCgamma2.

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Authors: Watanabe, D., Hashimoto, S., Ishiai, M., Matsushita, M., Baba, Y., Kishimoto, T., Kurosaki, T., & Tsukada, S.
Affiliations: The University of Osaka (JP)
Kansai Medical University (JP)
Corresponding author: Tsukada, Satoshi
ORCID: Ishiai, Masamichi
Matsushita, Masato
Baba, Yoshihiro
Kishimoto, Tadamitsu
Kurosaki, Tomohiro
Venue: Journal of Biological Chemistry
Publisher: Elsevier BV
Published: 2001-10
Volume: 276
Issue: 42
Pages: 38595-38601
ISSN: 0021-9258 (ISSN-L)
DOI: 10.1074/jbc.m103675200
OpenAlex: W2057525817
Cited by: 136
References: 57
Citations by year: 2026: 5 · 2025: 4 · 2024: 5 · 2023: 5 · 2022: 6 · 2021: 6 · 2020: 2 · 2019: 7 · 2018: 5 · 2017: 3 · 2016: 2 · 2015: 2 · 2014: 4 · 2013: 2 · 2012: 8
FWCI: 3.38
Type: journal article
Language: en
Open access: hybrid
doi.org
Licence: cc-by
www.elsevier.com/tdm/userlicense/1.0/ (tdm)
creativecommons.org/licenses/by/4.0/ (vor, 6940 d)
Locations: Journal of Biological Chemistry (publishedVersion, cc-by)
PubMed (publishedVersion)
Funders: Ministry of Education, Culture, Sports, Science and Technology
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
Life Sciences › Immunology and Microbiology › Immunology › Immunodeficiency and Autoimmune Disorders
Keywords: PLCγ2, Bruton's tyrosine kinase, tyrosine phosphorylation sites, B cell receptor signaling, calcium signaling, Syk, DT40 cells
MeSH terms: Agammaglobulinaemia Tyrosine Kinase, Amino Acid Sequence, Animals, Binding Sites, Calcium, Cell Line, Enzyme Activation, Genetic Vectors, Glutathione Transferase, Humans, Hydrolysis, Isoenzymes, Molecular Sequence Data, Mutation, Phenylalanine, Type C Phospholipases, Phosphorylation, Precipitin Tests, Protein-Tyrosine Kinases, Receptors, Antigen, B-Cell, Recombinant Fusion Proteins, Time Factors, Transfection, Tyrosine, Immunoblotting, Signal Transduction, Sequence Homology, Amino Acid, DNA, Complementary, Rats, Phospholipase C gamma

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Four Tyrosine Residues in Phospholipase C-γ2, Identified as Btk-dependent Phosphorylation Sites, Are Required for B Cell Antigen Receptor-coupled Calcium Signaling

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