Inflammasomes are multi-protein complexes that are responsible for the induction of proinflammatory cytokines and inflammatory cell death. They are unique in innate immune signaling because they can be triggered by a plethora of diverse signals from both pathogens and environmental danger. The research in our lab focuses on dissecting the molecular mechanisms of inflammasome pathways and studying how their dysfunction leads to defective host defense against various pathogenic microorganisms, as well as the impact on autoimmune diseases, neurodegeneration and metabolic syndromes.
Our lab utilizes diverse and complementary approaches, including biochemical assays, confocal fluorescence imaging, CRISPR knockout/rescue and animal models. Our recent study has uncovered the unexpected role of trans-Golgi network dispersion in inflammasome activation, and we are currently interested in studying how pathogens are able to evade or hijack these cellular signals to counter the host defense. We believe that these studies will unveil potential therapeutic targets for infectious diseases and many other human health problems.
UT Southwestern Medical Center
Dallas, TX
Postdoctoral Researcher - Immunology & Microbiology
2019
UT Southwestern Medical Center
Dallas, TX
Ph.D. - Biomedical Science
2014
Zhejiang University
Hangzhou, China
B.S. - Biotechnology
2009
PtdIns4P on dispersed trans-Golgi network mediates NLRP3 inflammasome activation.
PtdIns4P on dispersed trans-Golgi network mediates NLRP3 inflammasome activation. Nature. 2018 12; 564(7734):71-76.
PMID: 30487600
Detection of Microbial Infections Through Innate Immune Sensing of Nucleic Acids.
Detection of Microbial Infections Through Innate Immune Sensing of Nucleic Acids. Annu Rev Microbiol. 2018 Sep 08; 72:447-478.
PMID: 30200854
Prion-like polymerization underlies signal transduction in antiviral immune defense and inflammasome activation.
Prion-like polymerization underlies signal transduction in antiviral immune defense and inflammasome activation. Cell. 2014 Mar 13; 156(6):1207-1222.
PMID: 24630723
MAVS recruits multiple ubiquitin E3 ligases to activate antiviral signaling cascades.
MAVS recruits multiple ubiquitin E3 ligases to activate antiviral signaling cascades. Elife. 2013 Aug 14; 2:e00785.
PMID: 23951545
Regulation of NF-?B by ubiquitination.
Regulation of NF-?B by ubiquitination. Curr Opin Immunol. 2013 Feb; 25(1):4-12.
PMID: 23312890
Direct, noncatalytic mechanism of IKK inhibition by A20.
Direct, noncatalytic mechanism of IKK inhibition by A20. Mol Cell. 2011 Nov 18; 44(4):559-71.
PMID: 22099304
Production of TH1 and TH2 cell lines and clones.
Fitch FW, Gajewski TF, Hu-Li J. Production of TH1 and TH2 cell lines and clones. Curr Protoc Immunol. 2006 May; Chapter 3:Unit 3.13.
PMID: 22099304
Production of TH1 and TH2 cell lines and clones.
Fitch FW, Gajewski TF, Hu-Li J. Production of TH1 and TH2 cell lines and clones. Curr Protoc Immunol. 2006 May; Chapter 3:Unit 3.13.
PMID: 30487600
Production of TH1 and TH2 cell lines and clones.
Fitch FW, Gajewski TF, Hu-Li J. Production of TH1 and TH2 cell lines and clones. Curr Protoc Immunol. 2006 May; Chapter 3:Unit 3.13.
PMID: 30200854