STAP‐2 negatively regulates BCR‐mediated B cell activation by recruiting tyrosine‐protein kinase CSK to LYN

Author:

Kashiwakura Jun‐ichi12ORCID,Kawahara Shoya1,Inagaki Iori1,Inui Kyosuke1,Saitoh Kodai1,Kagohashi Kota1,Sasaki Yuto1,Kobayashi Fuki1,Kitai Yuichi1,Muromoto Ryuta1,Oritani Kenji3,Matsuda Tadashi1ORCID

Affiliation:

1. Department of Immunology, Graduate School of Pharmaceutical Sciences Hokkaido University Sapporo Hokkaido Japan

2. Department of Life Science, Faculty of Pharmaceutical Sciences Hokkaido University of Science Sapporo Hokkaido Japan

3. Department of Hematology International University of Health and Welfare Narita Chiba Japan

Abstract

Although signal‐transducing adaptor protein‐2 (STAP‐2) acts in certain immune responses, its role in B cell receptor (BCR)‐mediated signals remains unknown. In this study, we have revealed that BCR‐mediated signals, cytokine production and antibody production were increased in STAP‐2 knockout (KO) mice compared with wild‐type (WT) mice. Phosphorylation of tyrosine‐protein kinase LYN Y508 was reduced in STAP‐2 KO B cells after BCR stimulation. Mechanistic analysis revealed that STAP‐2 directly binds to LYN, dependently of STAP‐2 Y250 phosphorylation by LYN. Furthermore, phosphorylation of STAP‐2 enhanced interactions between LYN and tyrosine‐protein kinase CSK, resulting in enhanced CSK‐mediated LYN Y508 phosphorylation. These results suggest that STAP‐2 is crucial for controlling BCR‐mediated signals and antibody production by enhanced CSK‐mediated feedback regulation of LYN.

Funder

Japan Society for the Promotion of Science

Ministry of Education, Culture, Sports, Science and Technology

Publisher

Wiley

Subject

Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics

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