BBS Faculty Member - Hao Wu

Hao Wu

Department of Biological Chemistry and Molecular Pharmacology

Boston Children's Hospital
Center For Life Sciences Building, Room 3099
3 Blackfan Circle
Boston, MA 02115
Tel: 617-713-8160
Fax: 617-713-8161
Email: hao.wu@childrens.harvard.edu
Lab Members: 10 postdoctoral fellows, 4 graduate students, 2 technicians
Visit my lab page here.



The Wu laboratory of structural immunology focuses on elucidating the molecular mechanism of signal transduction by immune receptors, especially innate immune receptors. The lab began its studies on the signaling of a classical cytokine produced by the innate immune system, tumor necrosis factor (TNF), which induces diverse cellular responses such as NF-κB activation and cell death. Receptors for TNF belong to the large TNF receptor (TNFR) superfamily. The second pursuit of the lab has been the Toll-like receptor (TLR)/interleukin-1 receptor (IL-1R) superfamily, which induces signaling pathways overlapping with those of the TNFR superfamily. TLRs are transmembrane receptors that sense a discrete collection of molecules of microbial origin in the extracellular space and endosomes and members of IL-1R family are receptors for cytokines IL-1 and IL-18. TLRs and IL-1Rs share similar cytoplasmic domains. The lab recently expanded its research to a number of cytosolic pattern recognition receptors that provide intracellular surveillance of infections. Some of these intracellular sensors can induce pathways overlapping with those of TLRs such as activation of NF-κB and interferon regulatory factors. Others mediate the formation of inflammasomes that control activation of caspase-1, which in turn regulates maturation of the proinflammatory cytokines IL-1 and IL-18 and induces pyroptosis, a rapid inflammatory form of cell death.

The overall objective of the Wu lab has been to determine how macromolecular interactions mediate the transmission of signals from receptors to effectors to direct innate immune responses using the core approaches of structural biology. These structural studies challenge the traditional view of signal transduction as a string of recruitment and allosteric events. As a recurrent theme, the lab’s research revealed that upon ligand stimulation, many innate immune receptors assemble large oligomeric intracellular signaling complexes, or “signalosomes,” to induce the activation of caspases, kinases and ubiquitin ligases, leading to cell death, cytokine maturation or expression of gene products for immune and inflammatory responses. The different scaffolds identified by these structural studies provide a molecular foundation for understanding the formation of microscopically visible signaling clusters in cells.



Last Update: 8/22/2013



Publications

For a complete listing of publications click here.

 


 

Jixi Li, Thomas McQuade, Ansgar B. Siemer, Johanna Napetschnig, Kenta Moriwaki, Yu-Shan Hsiao, Ermelinda Damko, David Moquin, Thomas Walz, Ann McDermott, Francis Ka-Ming Chan, and Hao Wu (2012). The RIP1/RIP3 necrosome forms a functional amyloidal signaling complex required for programmed necrosis. Cell, 150: 339-350.

Qian Yin, Yuan Tian, Venkataraman Kabaleeswaran, Xiaomo Jiang, Daqi Tu, Michael J. Eck, Zhijian J. Chen and
Hao Wu (2012). Cyclic di-GMP sensing via the innate immune signaling protein STING. Mol Cell, 46: 735-45.

Guozhou Xu, Yu-Chih Lo, Qiubai Li, Gennaro Napolitano, Xuefeng Wu, Xuliang Jiang, Michel Dreano, Michael Karin and
Hao Wu (2011). Crystal structure of inhibitor of κB kinase β (IKKβ). Nature, 472: 325-30.

Su-Chang Lin, Yu-Chih Lo and
Hao Wu (2010). Helical assembly in the MyD88-IRAK4-IRAK2 complex in TLR/IL-1R signaling. Nature, 465: 885-90.



© 2013 by the President and Fellows of Harvard College