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Toll Receptor-Mediated Hippo Signaling Controls Innate Immunity in Drosophila
University of Massachusetts Medical School Faculty Publications
  • Bo Liu, Johns Hopkins University
  • Yonggang Zheng, Johns Hopkins University
  • Feng Yin, Johns Hopkins University
  • Jianzhong Yu, Johns Hopkins University
  • Neal S. Silverman, University of Massachusetts Medical School
  • Duojia Pan, Johns Hopkins University
UMMS Affiliation
Division of Infectious Diseases and Immunology, Department of Medicine
Publication Date
Document Type
The Hippo signaling pathway functions through Yorkie to control tissue growth and homeostasis. How this pathway regulates non-developmental processes remains largely unexplored. Here, we report an essential role for Hippo signaling in innate immunity whereby Yorkie directly regulates the transcription of the Drosophila IkappaB homolog, Cactus, in Toll receptor-mediated antimicrobial response. Loss of Hippo pathway tumor suppressors or activation of Yorkie in fat bodies, the Drosophila immune organ, leads to elevated cactus mRNA levels, decreased expression of antimicrobial peptides, and vulnerability to infection by Gram-positive bacteria. Furthermore, Gram-positive bacteria acutely activate Hippo-Yorkie signaling in fat bodies via the Toll-Myd88-Pelle cascade through Pelle-mediated phosphorylation and degradation of the Cka subunit of the Hippo-inhibitory STRIPAK PP2A complex. Our studies elucidate a Toll-mediated Hippo signaling pathway in antimicrobial response, highlight the importance of regulating IkappaB/Cactus transcription in innate immunity, and identify Gram-positive bacteria as extracellular stimuli of Hippo signaling under physiological settings.
DOI of Published Version
Cell. 2016 Jan 28;164(3):406-19. doi: 10.1016/j.cell.2015.12.029. Link to article on publisher's site
Related Resources
Link to Article in PubMed
PubMed ID
Citation Information
Bo Liu, Yonggang Zheng, Feng Yin, Jianzhong Yu, et al.. "Toll Receptor-Mediated Hippo Signaling Controls Innate Immunity in Drosophila" Vol. 164 Iss. 3 (2016) ISSN: 0092-8674 (Linking)
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