Unraveling the non-senescence phenomenon in Hydra

Journal of Theoretical Biology

Volumn 382, Issue , 2015, Pages 137-149

  Dańko, Maciej J ^a   Kozłowski, Jan ^b   Schaible, Ralf ^a  

^a MAX PLANCK INSTITUTE FOR DEMOGRAPHIC RESEARCH   (Germany)

^b JAGIELLONIAN UNIVERSITY   (Poland)

Author keywords

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

Indexed keywords

ASEXUAL REPRODUCTION; CLONAL ORGANISM; MORTALITY;

ARTICLE; ASEXUAL REPRODUCTION; CELL ACTIVITY; CELL AGING; CELL BUDDING; CELL COUNT; CELL DAMAGE; CELL DEATH; CELL DIFFERENTIATION; CELL ISOLATION; CELL REGENERATION; CELL RENEWAL; CELL SELECTION; CELL TRANSFORMATION; CELLS BY BODY ANATOMY; CELLULAR DISTRIBUTION; HYDRA; NONHUMAN; PHENOMENOLOGY; PRIORITY JOURNAL; STEM CELL; ANATOMY AND HISTOLOGY; ANIMAL; BIOLOGICAL MODEL; BODY SIZE; CELL CLONE; CELL DIVISION; CYTOLOGY; GROWTH, DEVELOPMENT AND AGING; LONGEVITY; PHYSIOLOGY; PROBABILITY; REPRODUCTION;

HYDRA; METAZOA;

ANIMALS; BODY SIZE; CELL DEATH; CELL DIFFERENTIATION; CELL DIVISION; CLONE CELLS; HYDRA; LONGEVITY; MODELS, BIOLOGICAL; PROBABILITY; REPRODUCTION;

EID: 84937242973     PISSN: 00225193     EISSN: 10958541     Source Type: Journal    
DOI: 10.1016/j.jtbi.2015.06.043     Document Type: Article

References (62)

1. Alonso L., Fuchs E. Stem cells of the skin epithelium. Proc. Natl. Acad. Sci. USA 2003, 100:11830-11835.
2. Arai, F., and Suda, T., 2008. Quiescent stem cells in the niche StemBook [Internet].
3. Arnheim N., Cortopassi G. Deleterious mitochondrial DNA mutations accumulate in aging human tissues. Mutat. Res. 1992, 275:157-167.
4. Asaithamby A., Chen D.J. Cellular responses to DNA double-strand breaks after low-dose gamma-irradiation. Nucleic Acids Res. 2009, 37:3912-3923.
5. Bandy B., Davison A. Mitochondrial mutations may increase oxidative stress: implications for carcinogenesis and aging?. Free Radic. Biol. Med. 1990, 8:523-539.
6. Beltrami A.P., Cesselli D., Beltrami C.A. At the stem of youth and health. Pharmacol. Ther. 2011, 129:3-20.
7. Blanpain C., Mohrin M., Sotiropoulou P.A., Passegue E. DNA-Damage Response in Tissue-Specific and Cancer Stem Cells. Cell Stem Cell 2011, 8:16-29.
8. Bode H., Berking S., David C.N., Gierer A., Schaller H., Trenkner E. Quantitative analysis of cell types during growth and morphogenesis in Hydra. Wilhelm Roux' Arch. Entwicklungsmechanik Org. 1973, 171:269-285.
9. Bode H.R. The interstitial cell lineage of hydra: a stem cell system that arose early in evolution. J. Cell Sci. 1996, 109:1155-1164.
10. Bode H.R., Flick K.M., Bode P.M. Constraints on relative sizes of cell populations in Hydra attenuata. J. Cell Sci. 1977, 24:31-50.
11. Boettger A., Strasser D., Alexandrova O., Levin A., Fischer S., Lasi M., Rudd S., David C.N. Genetic screen for signal peptides in Hydra reveals novel secreted proteins and evidence for non-classical protein secretion. Eur. J. Cell Biol. 2006, 85:1107-1117.
12. Bosch T.C.G., David C.N. Growth-regulation in Hydra - relationship between epithelial-cell cycle length and growth-rate. Dev. Biol. 1984, 104:161-171.
13. Bosch T.C.G., David C.N. Stem-cells of Hydra magnipapillata can differentiate into somatic cells and germ line cells. Dev. Biol. 1987, 121:182-191.
14. Bosch T.C.G., Anton-Erxleben F., Hemmrich G., Khalturin K. The Hydra polyp: nothing but an active stem cell community. Dev. Growth Differ. 2010, 52:15-25.
15. Campbell R.D. Tissue dynamics of steady state growth in Hydra littoralis. I. Patterns of cell division. Dev. Biol. 1967, 15:487.
16. Casali A., Batlle E. Intestinal stem cells in mammals and Drosophila. Cell Stem Cell 2009, 4:124-127.
17. Cichoń M. Evolution of longevity through optimal resource allocation. Proc. R. Soc. B: Biol. Sci. 1997, 264:1383-1388.
18. David C.N. Interstitial stem cells in Hydra: multipotency and decision-making. Int. J. Dev. Biol. 2012, 56:489-497.
19. David C.N., Campbell R.D. Cell cycle kinetics and development of Hydra attenuata.1. Epithelial cells. J. Cell Sci. 1972, 11:557.
20. Doupe D.P., Klein A.M., Simons B.D., Jones P.H. The ordered architecture of murine ear epidermis is maintained by progenitor cells with random fate. Dev. Cell 2010, 18:317-323.
21. Feinendegen L.E. Evidence for beneficial low level radiation effects and radiation hormesis. Br. J. Radiol. 2005, 78:3-7.
22. Feinendegen L.E., Pollycove M., Neumann R.D. Whole-body responses to low-level radiation exposure: new concepts in mammalian radiobiology. Exp. Hematol. 2007, 35:37-46.
23. Freitas A.A., de Magalhaes J.P. A review and appraisal of the DNA damage theory of ageing. Mutat. Res.-Rev. Mutat. Res. 2011, 728:12-22.
24. Galliot B., Ghila L. Cell plasticity in homeostasis and regeneration. Mol. Reprod. Dev. 2010, 77:837-855.
25. Goodell M.A. Stem-cell "plasticity": befuddled by the muddle. Curr. Opin. Hematol. 2003, 10:208-213.
26. Hamilton W.D. Moulding of senescence by natural selection. J. Theor. Biol. 1966, 12:12.
27. Henriquez-Hernandez L.A., Carmona-Vigo R., Pinar B., Bordon E., Lloret M., Nunez M.I., Rodriguez-Gallego C., Lara P.C. Combined low initial DNA damage and high radiation-induced apoptosis confers clinical resistance to long-term toxicity in breast cancer patients treated with high-dose radiotherapy. Radiat. Oncol. 2011, 6.
28. Herzog E.L., Chai L., Krause D.S. Plasticity of marrow-derived stem cells. Blood 2003, 102:3483-3493.
29. Hobmayer B., Jenewein M., Eder D., Eder M.-K., Glasauer S., Gufler S., Hartl M., Salvenmoser W. Stemness in Hydra - a current perspective. Int. J. Dev. Biol. 2012, 56:509-517.
30. Jones O.R., Scheuerlein A., Salguero-Gómez R., Giovanni Camarda C., Schaible R., Brenda C., Dahlgren J.P., Ehrlén J., García M.G., Menges E., Quintana-Ascencio P.F., Caswell H., Baudisch A., Vaupel J.W. Diversity of ageing across the tree of life. Nature 2014, 505:169-173.
31. Kimura, M., and Ohta, T., 1971. Theoretical aspects of population genetics. In: Monographs in Population Biology. Princeton University Press. Princeton, N.J, USA.
32. Kirkwood T.B.L. Evolution of aging. Nature 1977, 270:301-304.
33. Klein A.M., Simons B.D. Universal patterns of stem cell fate in cycling adult tissues. Development 2011, 138:3103-3111.
34. Kowald A., Kirkwood T.B.L. Accumulation of defective mitochondria through delayed degradation of damaged organelles and its possible role in the ageing of post-mitotic and dividing cells. J. Theor. Biol. 2000, 202:145-160.
35. Kucia M., Reca R., Miekus K., Wanzeck J., Wojakowski W., Janowska-Wieczorek A., Ratajczak J., Ratajczak M.Z. Trafficking of normal stem cells and metastasis of cancer stem cells involve similar mechanisms: pivotal role of the SDF-1-CXCR4 axis. Stem Cells 2005, 23:879-894.
36. Lorat Y., Schanz S., Schuler N., Wennemuth G., Rube C., Rube C.E. Beyond repair foci: DNA double-strand break repair in euchromatic and heterochromatic compartments analyzed by transmission electron microscopy. PLoS One 2012, 7:e38165.
37. Łomnicki A., Slobodkin L.B. Floating in Hydra Littoralis. Ecology 1966, 47:881-889.
38. Martinez D.E. Mortality patterns suggest lack of senescence in hydra. Exp. Gerontol. 1998, 33:217-225.
39. Martínez D.E., Levinton J.S. Asexual metazoans undergo senescence. Proc. Natl. Acad. Sci. USA 1992, 89:9920-9923.
40. Medawar P.B. An Unsolved Problem of Biology 1952, H.K. Lewis and Company, London.
41. Morrison S.J., Spradling A.C. Stem cells and niches: mechanisms that promote stem cell maintenance throughout life. Cell 2008, 132:598-611.
42. Mylius S.D., Diekmann O. On evolutionary stable life histories, optimization and the need to be specific about density dependence. Oikos 1995, 74:218-224.
43. Nishimiya-Fujisawa C., Kobayashi S. Germline stem cells and sex determination in Hydra. Int. J. Dev. Biol. 2012, 56:499-508.
44. Orlowski C., Mah L.J., Vasireddy R.S., El-Osta A., Karagiannis T.C. Double-strand breaks and the concept of short- and long-term epigenetic memory. Chromosoma 2011, 120:129-149.
45. Otto J.J., Campbell R.D. Tissue economics of Hydra - regulation of cell-cycle, animal size and development by controlled feeding rates. J. Cell Sci. 1977, 28:117-132.
46. Pinar B., Henriquez-Hernandez L.A., Lara P.C., Bordon E., Rodriguez-Gallego C., Lloret M., Nunez M.I., De Almodovar M.R. Radiation induced apoptosis and initial DNA damage are inversely related in locally advanced breast cancer patients. Radiat. Oncol. 2010, 5.
47. Rando T.A. Stem cells, ageing and the quest for immortality. Nature 2006, 441:1080-1086.
48. Rothkamm K., Lobrich M. Evidence for a lack of DNA double-strand break repair in human cells exposed to very low x-ray doses. Proc. Natl. Acad. Sci. USA 2003, 100:5057-5062.
49. Rube C.E., Fricke A., Widmann T.A., Furst T., Madry H., Pfreundschuh M., Rube C. Accumulation of DNA damage in hematopoietic stem and progenitor cells during human aging. PLoS One 2011, 6.
50. Sancar A., Lindsey-Boltz L.A., Unsal-Kacmaz K., Linn S. Molecular mechanisms of mammalian DNA repair and the DNA damage checkpoints. Ann. Rev. Biochem. 2004, 73:39-85.
51. Schaible R., Ringelhan F., Kramer H.B., Miethe T. Environmental challenges improve resource utilization for asexual reproduction and maintenance in hydra. Exp. Gerontol. 2011, 46:794-802.
52. Schaible R., Sussmann M., Kramer H.B. Aging and potential for self-renewal: Hydra living in the age of aging - a mini-review. Gerontology 2014, 60:548-556.
53. Seluanov A., Mittelman D., Pereira-Smith O.M., Wilson J.H., Gorbunova V. DNA end joining becomes less efficient and more error-prone during cellular senescence. Proc. Natl. Acad. Sci. USA 2004, 101:7624-7629.
54. Simmons R.A., Suponitsky-Kroyter I., Selak M.A. Progressive accumulation of mitochondrial DNA mutations and decline in mitochondrial function lead to beta-cell failure. J. Biol. Chem. 2005, 280:28785-28791.
55. Singh N.P., Ogburn C.E., Wolf N.S., van Belle G., Martin G.M. DNA double-strand breaks in mouse kidney cells with age. Biogerontology 2001, 2:261-270.
56. Steele R.E. Developmental signaling in Hydra: what does it take to build a "simple" animal?. Dev. Biol. 2002, 248:199-219.
57. Sugiyama S., Hattori K., Hayakawa M., Ozawa T. Quantitative analysis of age-associated accumulation of mitochondrial DNA with deletion in human hearts. Biochem. Biophys. Res. Commun. 1991, 180:894-899.
58. Takahashi T., Koizumi O., Ariura Y., Romanovitch A., Bosch T.C.G., Kobayakawa Y., Mohri S., Bode H.R., Yum S., Hatta M., Fujisawa T. A novel neuropeptide, Hym-355, positively regulates neuron differentiation in Hydra. Development 2000, 127:997-1005.
59. Technau U., Steele R.E. Evolutionary crossroads in developmental biology: Cnidaria. Development 2011, 138:1447-1458.
60. Torudd J., Protopopova M., Sarimov R., Nygren J., Eriksson S., Markova E., Chovanec M., Selivanova G., Belyaev I.Y. Dose-response for radiation-induced apoptosis, residual 53BP1 foci and DNA-loop relaxation in human lymphocytes. Int. J. Radiat. Biol. 2005, 81:125-138.
61. Wagers A.J., Weissman I.L. Plasticity of adult stem cells. Cell 2004, 116:639-648.
62. Williams G.C. Pleiotropy, natural selection, and the evolution of senescence. Evolution 1957, 11:398-411.