Tespa1 negatively regulates FcεRI-mediated signaling and the mast cell-mediated allergic response
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Updated: Apr 20, 2026

Analyzing the Functions of Mast Cells In Vivo Using 'Mast Cell Knock-in' Mice
Published on: May 27, 2015
Di Wang1, Mingzhu Zheng2, Yuanjun Qiu2
1Institute of Immunology, Program in Molecular and Cellular Biology, Department of Pathology and Pathophysiology, and Department of Biochemistry and Molecular Biology, Zhejiang University School of Medicine, Hangzhou 310058, China Institute of Immunology, Program in Molecular and Cellular Biology, Department of Pathology and Pathophysiology, and Department of Biochemistry and Molecular Biology, Zhejiang University School of Medicine, Hangzhou 310058, China diwang@zju.edu.cn lu_linrong@zju.edu.cn.
Abstract:
Antigen-mediated cross-linking of IgE on mast cells triggers a signaling cascade that results in their degranulation and proinflammatory cytokine production, which are key effectors in allergic reactions. We show that the activation of mast cells is negatively regulated by the newly identified adaptor protein Tespa1. Loss of Tespa1 in mouse mast cells led to hyper-responsiveness to stimulation via FcεRI. Mice lacking Tespa1 also displayed increased sensitivity to IgE-mediated allergic responses. The dysregulated signaling in KO mast cells was associated with increased activation of Grb2-PLC-γ1-SLP-76 signaling within the LAT1 (linker for activation of T cells family, member 1) signalosome versus the LAT2 signalosome. Collectively, these findings show that Tespa1 orchestrates mast cell activation by tuning the balance of LAT1 and LAT2 signalosome assembly.
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