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Weiguo Zhang

Associate Professor
Research Interest: 
Developmental biology
Signal transduction
Research Summary: 
Adaptor proteins in immunoreceptor-mediated signaling, cellular activation, and development of autoimmunity
Research Description: 

Activation via the T-cell antigen receptor (TCR) triggers a cascade of intracellular biochemical events eventually leading to T-cell proliferation and effector functions. One of the earliest events is the activation of the Src family tyrosine kinases Fyn and Lck. The activated Src family kinases phosphorylate the CD3 subunits and TCRζ chains. ZAP-70 tyrosine kinase is recruited to the antigen receptors via the binding to CD3 and TCRζ. ZAP-70 is then tyrosine phosphorylated by these Src family kinases and thus activated. These activated tyrosine kinases further phosphorylate a number of intracellular proteins, such as PLC-γ1, Vav, Cbl, SLP-76, and LAT, and activate downstream signaling pathways including the Ras-MAPK pathway and Ca2+flux. Activation of these two pathways is required for AP-1 and NFAT-mediated transcription, IL-2 production, and T-cell proliferation.

Our primary interest of the laboratory is to understand the role of membrane-associated adaptor proteins in lymphocyte activation, development, and immune response. One of these proteins is LAT (Linker for Activation of T-cells). LAT is tyrosine phosphorylated upon T-cell activation and associates with several signaling molecules including Grb2, Gads, and PLC-γ1. LAT-deficient T-cells are defective in the Ras-MAPK activation and Ca2+ flux after the TCR engagement. LAT knockout mice have an early block in thymocyte development. Interestingly, mice with a mutation in LAT develop a severe autoimmune disease. We are investigating how LAT interacts with other signaling proteins and how LAT regulates T cell activation and immune responses.

In addition to LAT, we are working on two LAT-like molecules, LAB and LAX. We have generated mice deficient in these proteins and are analyzing the phenotypes of these mice to determine the role of these proteins in lymphocyte signaling and immune responses.

Our long-term goal is to understand the details of immunoreceptor-mediated signaling pathways. Understanding these signaling pathways may identify therapeutic targets that could facilitate the development of drugs that suppress, modify, or augment immune responses in autoimmunity, transplantation, allergy, and cancer.

Tyrosine Phosphorylation-Independent Regulation of Lipopolysaccharide-Mediated Response by the Transmembrane Adaptor Protein LAB.
Zhu M, Fuller DM, Ou-Yang CW, Sullivan SA, Zhang W.
J Immunol. 2012. 188:2733-41.

A tale of two TRAPs: LAT and LAB in the regulation of lymphocyte development, activation, and autoimmunity.
Fuller DM, Zhu M, Ou-Yang CW, Sullivan SA, Zhang W.
Immunol Res. 2011. 49:97-108.

The role of the LAT-PLC-gamma1 interaction in T regulatory cell function.
Chuck MI, Zhu M, Shen S, Zhang W.
J Immunol. 2010. 184:2476-86.

Negative regulation of T cell activation and autoimmunity by the transmembrane adaptor protein LAB.
Zhu M, Koonpaew S, Liu Y, Shen S, Denning T, Dzhagalov I, Rhee I, Zhang W.
Immunity. 2006. 25:757-68.

LAT-mediated signaling in CD4+CD25+ regulatory T cell development.
Koonpaew S, Shen S, Flowers L, Zhang W.
J Exp Med. 2006. 203:119-29.