PTPN22 mediates delayed negative feedback of T cell activation by forming an inhibitory signaling complex
PTPN22 is a cytosolic tyrosine phosphatase expressed in immune cells that negatively regulates T cell receptor (TCR) signaling and implicated in autoimmune diseases through a common (R620W) variant. The molecular mechanisms by which PTPN22 modulates TCR activation remain incompletely understood. Here we show that upon T cell activation, PTPN22 forms delayed clusters at TCR microclusters (MCs) alongside Csk, STS-1 and PSTPIP, constituting a feedback inhibitory complex. Using imaging analyses, MS, and knockout mouse models, we demonstrate that this complex functions as a delayed negative regulation of TCR signaling, and that autoimmune-associated PTPN22 (R620W) mutant exhibits reduced binding to Csk and STS-1, impairing complex formation. Consequently, T cells expressing the mutant display enhanced cytokine production and immune responses. These findings reveal cooperative inhibitory mechanism involving PTPN22 and its partners that modulates T cell activation, providing insights into how PTPN22 variants contribute to autoimmune disease susceptibility.
Authors
- Natsuko Tanimura
- Akiko Soneda Hashimoto (ORCID: https://orcid.org/0000-0001-8519-266X)
- Yusuke Kawashima (ORCID: https://orcid.org/0000-0002-9779-8199)
- Natsumi Yoneda
- Takashi Saito (ORCID: https://orcid.org/0000-0001-9495-3547)
- Osamu Ohara (ORCID: https://orcid.org/0000-0002-3328-9571)
- Machie Sakuma
- Manabu Nakayama (ORCID: https://orcid.org/0009-0001-0488-1664)
- Haruhiko Koseki
- Bernard Malissen
Institutions
- MSD K.K. (Japan) (JP)
- Centre d’Immunologie de Marseille-Luminy (FR)
- Kazusa DNA Research Institute (JP)
- RIKEN Center for Integrative Medical Sciences (JP)
Publication Details
- Journal
- International Immunology
- Published
- 2026-09-25
- DOI
- https://doi.org/10.1093/intimm/dxag050
- Primary Topic
- Diabetes and associated disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00