Elsevier

Journal of Theoretical Biology

Volume 382, 7 October 2015, Pages 137-149
Journal of Theoretical Biology

Unraveling the non-senescence phenomenon in Hydra

https://doi.org/10.1016/j.jtbi.2015.06.043Get rights and content
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Highlights

  • Hydra shows no signs of senescence under laboratory conditions.

  • Within-cell repair is imperfect and cannot solely protect against damage accumulation.

  • Cellular damage drift leads to accumulation of damaged cell lineages, hence senescence.

  • High prevalence and continued division of Hydra׳s stem cells act against damage drift.

  • These features and efficient selection against damaged cells are crucial for non-senescence.

Abstract

Unlike other metazoans, Hydra does not experience the distinctive rise in mortality with age known as senescence, which results from an increasing imbalance between cell damage and cell repair. We propose that the Hydra controls damage accumulation mainly through damage-dependent cell selection and cell sloughing. We examine our hypothesis with a model that combines cellular damage with stem cell renewal, differentiation, and elimination. The Hydra individual can be seen as a large single pool of three types of stem cells with some features of differentiated cells. This large stem cell community prevents “cellular damage drift,” which is inevitable in complex conglomerate (differentiated) metazoans with numerous and generally isolated pools of stem cells. The process of cellular damage drift is based on changes in the distribution of damage among cells due to random events, and is thus similar to Muller׳s ratchet in asexual populations. Events in the model that are sources of randomness include budding, cellular death, and cellular damage and repair. Our results suggest that non-senescence is possible only in simple Hydra-like organisms which have a high proportion and number of stem cells, continuous cell divisions, an effective cell selection mechanism, and stem cells with the ability to undertake some roles of differentiated cells.

Keywords

Cellular damage drift
Immortality
Programmed cell death
Clonal organism
Muller׳s ratchet

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