The E3 ligases Itch and WWP2 cooperate to limit T.sub.H2 differentiation by enhancing signaling through the TCR

• Published in: Nature immunology Vol. 19; no. 7; pp. 766 - 1531
• Main Authors: Aki, Daisuke, Li, Hui, Zhang, Wen, Zheng, Mingke, Elly, Chris, Lee, Jee H, Zou, Weiguo
• Format: Journal Article
• Language: English
• Published: Nature Publishing Group 01.07.2018
• Subjects: Antigens; Autoimmunity; Cell differentiation; Genetic aspects; Inflammation; Ligases; Phenols (Class of compounds); Phosphatases; Physiological aspects; T cell antigen receptors; T cells; Tyrosine; Ubiquitin; United States; China
• ISSN: 1529-2908; 1529-2916
• DOI: 10.1038/s41590-018-0137-8

The mechanisms by which the sensitivity of naive CD4.sup.+ T cells to stimulation by the cognate antigen via the T cell antigen receptor (TCR) determines their differentiation into distinct helper T cell subsets remain elusive. Here we demonstrate functional collaboration of the ubiquitin E3 ligases Itch and WWP2 in regulating the strength of the TCR signal. Mice lacking both Itch and WWP2 in T cells showed spontaneous autoimmunity and lung inflammation. CD4.sup.+ T cells deficient in Itch and WWP2 exhibited hypo-responsiveness to TCR stimulation and a bias toward differentiation into the T.sub.H2 subset of helper T cells. Itch and WWP2 formed a complex and cooperated to enhance TCR-proximal signaling by catalyzing the conjugation of atypical ubiquitin chains to the phosphatase SHP-1 and reducing the association of SHP-1 with the tyrosine kinase Lck. These findings indicate that targeted ubiquitination regulates the strength of the TCR signal and differentiation toward the T.sub.H2 lineage.