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Cell Stem Cell
Article
License: Elsevier Non-Commercial
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Cell Stem Cell
Article . 2008
License: Elsevier Non-Commercial
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Cell Stem Cell
Article . 2008 . Peer-reviewed
License: Elsevier Non-Commercial
Data sources: Crossref
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JNK Activity in Somatic Stem Cells Causes Loss of Tissue Homeostasis in the Aging Drosophila Gut

Authors: Biteau, Benoît; Hochmuth, Christine E.; Jasper, Heinrich;

JNK Activity in Somatic Stem Cells Causes Loss of Tissue Homeostasis in the Aging Drosophila Gut

Abstract

Metazoans employ cytoprotective and regenerative strategies to maintain tissue homeostasis. Understanding the coordination of these strategies is critical to developing accurate models for aging and associated diseases. Here we show that cytoprotective Jun N-terminal kinase (JNK) signaling influences regeneration in the Drosophila gut by directing proliferation of intestinal stem cells (ISCs). Interestingly, this function of JNK contributes to the loss of tissue homeostasis in old and stressed intestines by promoting the accumulation of misdifferentiated ISC daughter cells. Ectopic Delta/Notch signaling in these cells causes their abnormal differentiation but also limits JNK-induced proliferation. Protective JNK signaling and control of cell proliferation and differentiation by Delta/Notch signaling thus have to be carefully balanced to ensure tissue homeostasis. Our findings suggest that this balance is lost in old animals, increasing the potential for neoplastic transformation.

Related Organizations
Keywords

Aging, MAP Kinase Kinase 4, Animals, Genetically Modified, Genetics, Animals, Drosophila Proteins, Homeostasis, Regeneration, Intestinal Mucosa, Cell Proliferation, Receptors, Notch, Intracellular Signaling Peptides and Proteins, Membrane Proteins, Cell Differentiation, Cell Biology, STEMCELL, Intestines, Adult Stem Cells, Oxidative Stress, Drosophila melanogaster, SIGNALING, Molecular Medicine, Signal Transduction

  • BIP!
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    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    530
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 0.1%
    influence
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    Top 1%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 1%
Powered by OpenAIRE graph
citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
530
Top 0.1%
Top 1%
Top 1%
hybrid