We are upgrading the repository! The content freeze has been extended to December 11, 2024, when we expect the new repository to become available. New submissions or changes to existing items will not be allowed until after the new website goes live. All content already published will remain publicly available for searching and downloading. Updates will be posted in the Website Upgrade 2024 FAQ in the sidebar Help menu. Reach out to escholarship@umassmed.edu with any questions.

Show simple item record

dc.contributor.authorLiu, Bo
dc.contributor.authorZheng, Yonggang
dc.contributor.authorYin, Feng
dc.contributor.authorYu, Jianzhong
dc.contributor.authorSilverman, Neal
dc.contributor.authorPan, Duojia
dc.date2022-08-11T08:08:20.000
dc.date.accessioned2022-08-23T15:51:37Z
dc.date.available2022-08-23T15:51:37Z
dc.date.issued2016-01-28
dc.date.submitted2017-03-07
dc.identifier.citation<p>Cell. 2016 Jan 28;164(3):406-19. doi: 10.1016/j.cell.2015.12.029. <a href="https://doi.org/10.1016/j.cell.2015.12.029">Link to article on publisher's site</a></p>
dc.identifier.issn0092-8674 (Linking)
dc.identifier.doi10.1016/j.cell.2015.12.029
dc.identifier.pmid26824654
dc.identifier.urihttp://hdl.handle.net/20.500.14038/28945
dc.description.abstractThe 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.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=26824654&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4733248/
dc.subjectImmunity
dc.titleToll Receptor-Mediated Hippo Signaling Controls Innate Immunity in Drosophila
dc.typeJournal Article
dc.source.journaltitleCell
dc.source.volume164
dc.source.issue3
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/faculty_pubs/1172
dc.identifier.contextkey9801488
html.description.abstract<p>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.</p>
dc.identifier.submissionpathfaculty_pubs/1172
dc.contributor.departmentDivision of Infectious Diseases and Immunology, Department of Medicine
dc.source.pages406-19


Files in this item

Thumbnail
Name:
Publisher version

This item appears in the following Collection(s)

Show simple item record