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FoxO is a critical regulator of stem cell maintenance in immortal Hydra.


ABSTRACT: Hydra's unlimited life span has long attracted attention from natural scientists. The reason for that phenomenon is the indefinite self-renewal capacity of its stem cells. The underlying molecular mechanisms have yet to be explored. Here, by comparing the transcriptomes of Hydra's stem cells followed by functional analysis using transgenic polyps, we identified the transcription factor forkhead box O (FoxO) as one of the critical drivers of this continuous self-renewal. foxO overexpression increased interstitial stem cell and progenitor cell proliferation and activated stem cell genes in terminally differentiated somatic cells. foxO down-regulation led to an increase in the number of terminally differentiated cells, resulting in a drastically reduced population growth rate. In addition, it caused down-regulation of stem cell genes and antimicrobial peptide (AMP) expression. These findings contribute to a molecular understanding of Hydra's immortality, indicate an evolutionarily conserved role of FoxO in controlling longevity from Hydra to humans, and have implications for understanding cellular aging.

SUBMITTER: Boehm AM 

PROVIDER: S-EPMC3511741 | biostudies-literature | 2012 Nov

REPOSITORIES: biostudies-literature

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FoxO is a critical regulator of stem cell maintenance in immortal Hydra.

Boehm Anna-Marei AM   Khalturin Konstantin K   Anton-Erxleben Friederike F   Hemmrich Georg G   Klostermeier Ulrich C UC   Lopez-Quintero Javier A JA   Oberg Hans-Heinrich HH   Puchert Malte M   Rosenstiel Philip P   Wittlieb Jörg J   Bosch Thomas C G TC  

Proceedings of the National Academy of Sciences of the United States of America 20121112 48


Hydra's unlimited life span has long attracted attention from natural scientists. The reason for that phenomenon is the indefinite self-renewal capacity of its stem cells. The underlying molecular mechanisms have yet to be explored. Here, by comparing the transcriptomes of Hydra's stem cells followed by functional analysis using transgenic polyps, we identified the transcription factor forkhead box O (FoxO) as one of the critical drivers of this continuous self-renewal. foxO overexpression incre  ...[more]

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