Toll signalling controls intestinal regeneration in Drosophila

The intestinal interphase is where epithelial renewal and tissue maintenance are balanced alongside immunological regulation. How these functions integrate with cellular signalling is under investigation. Here, we studied the role of the evolutionarily conserved innate immune Toll/NF-κB pathway in D...

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Autori principali: Udayakumar, Aiswarya (Autore) , Stavropoulos, Filippos (Autore) , Hadjipanteli, Theodosia (Autore) , Peng, Guofan (Autore) , Bahuguna, Shivohum (Autore) , MacClay, Caitlin (Autore) , Lee, Jeffrey Y. (Autore) , Xiao, Qi (Autore) , Xia, Yuxian (Autore) , Boutros, Michael (Autore) , Zhou, Jun (Autore) , Apidianakis, Yiorgos (Autore) , Pitsouli, Chrysoula (Autore) , Ligoxygakis, Petros (Autore)
Natura: Article (Journal)
Lingua:inglese
Pubblicazione: 19 January 2026
In: Development
Year: 2026, Volume: 153, Fascicolo: 2, Pages: 1-13
ISSN:1477-9129
DOI:10.1242/dev.204794
Accesso online:Verlag, kostenfrei, Volltext: https://doi.org/10.1242/dev.204794
Verlag, kostenfrei, Volltext: https://journals.biologists.com/dev/article/153/2/dev204794/370404/Toll-signalling-controls-intestinal-regeneration
Testo
Note sull'autore:Aiswarya Udayakumar, Filippos Stavropoulos, Theodosia Hadjipanteli, Guofan Peng, Shivohum Bahuguna, Caitlin MacClay, Jeffrey Y. Lee, Qi Xiao, Yuxian Xia, Michael Boutros, Jun Zhou, Yiorgos Apidianakis, Chrysoula Pitsouli, and Petros Ligoxygakis
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Riassunto:The intestinal interphase is where epithelial renewal and tissue maintenance are balanced alongside immunological regulation. How these functions integrate with cellular signalling is under investigation. Here, we studied the role of the evolutionarily conserved innate immune Toll/NF-κB pathway in Drosophila intestinal regeneration. We found that the core components of the canonical Toll pathway were necessary for intestinal stem cell (ISC) mitosis in homeostasis and upon infection. Toll activation was sufficient to push ISCs into mitosis and the enteroblast (EB) fate, but blocked EB differentiation resulting in ISC and EB accumulation. This was mediated by JNK and Akt/TOR signalling. When JNKK, JNK, Akt or TOR activity was reduced in gut progenitors, ISC mitosis was suppressed. Toll activation also triggered suppression of antimicrobial lysozyme and amidase genes, which led to increased gut bacterial density. Our results identify Toll as necessary and sufficient for ISC mitosis. Our model is that the Toll pathway acts as a regulator of the intestinal landscape integrating JNK and Akt signals to achieve gut tissue renewal and control of commensal bacteria density.
Descrizione del documento:Gesehen am 08.06.2026
Descrizione fisica:Online Resource
ISSN:1477-9129
DOI:10.1242/dev.204794