Biological immortality (sometimes referred to as bio-indefinite mortality) is a state in which the rate of mortality from senescence is stable or decreasing, thus decoupling it from chronological age. Various unicellular and multicellular species, including some vertebrates, achieve this state either throughout their existence or after living long enough. A biologically immortal living being can still die from means other than senescence, such as through injury, poison, disease, predation, lack of available resources, or changes to environment.

This definition of immortality has been challenged in the Handbook of the Biology of Aging,[1] because the increase in rate of mortality as a function of chronological age may be negligible at extremely old ages, an idea referred to as the late-life mortality plateau. The rate of mortality may cease to increase in old age, but in most cases that rate is typically very high.[2]

The term is also used by biologists to describe cells that are not subject to the Hayflick limit on how many times they can divide.

Cell lines

Main articles: Cell culture and Immortalised cell line

Biologists chose the word "immortal" to designate cells that are not subject to the Hayflick limit, the point at which cells can no longer divide due to DNA damage or shortened telomeres. Prior to Leonard Hayflick's theory, Alexis Carrel hypothesized that all normal somatic cells were immortal.[3]

The term "immortalization" was first applied to cancer cells that expressed the telomere-lengthening enzyme telomerase, and thereby avoided apoptosis—i.e. cell death caused by intracellular mechanisms. Among the most commonly used cell lines are HeLa and Jurkat, both of which are immortalized cancer cell lines.[4] These cells have been and still are widely used in biological research such as creation of the polio vaccine,[5] sex hormone steroid research,[6] and cell metabolism.[7] Embryonic stem cells and germ cells have also been described as immortal.[8][9]

Immortal cell lines of cancer cells can be created by induction of oncogenes or loss of tumor suppressor genes. One way to induce immortality is through viral-mediated induction of the large T-antigen,[10] commonly introduced through simian virus 40 (SV-40).[11]

Organisms

According to the Animal Aging and Longevity Database, the list of animals with negligible aging (along with estimated longevity in the wild) includes:[12]

In 2018, scientists working for Calico, a company owned by Alphabet, published a paper in the journal eLife which presents possible evidence that Heterocephalus glaber (Naked mole rat) do not face increased mortality risk due to aging.[13][14][15]

Bacteria and some yeast

Many unicellular organisms age: as time passes, they divide more slowly and ultimately die. Asymmetrically dividing bacteria and yeast also age. However, symmetrically dividing bacteria and yeast can be biologically immortal under ideal growing conditions.[16] In these conditions, when a cell splits symmetrically to produce two daughter cells, the process of cell division can restore the cell to a youthful state. However, if the parent asymmetrically buds off a daughter only the daughter is reset to the youthful state—the parent is not restored and will go on to age and die. In a similar manner stem cells and gametes can be regarded as "immortal".

Hydra

Hydra

Hydras are a genus of the Cnidaria phylum. All cnidarians can regenerate, allowing them to recover from injury and to reproduce asexually. Hydras are simple, freshwater animals possessing radial symmetry and contain post-mitotic cells (cells that will never divide again) only in the extremities.[17] All hydra cells continually divide.[18] It has been suggested that hydras do not undergo senescence, and, as such, are biologically immortal. In a four-year study, 3 cohorts of hydra did not show an increase in mortality with age. It is possible that these animals live much longer, considering that they reach maturity in 5 to 10 days.[19] However, this does not explain how hydras are subsequently able to maintain telomere lengths.

Jellyfish

Turritopsis dohrnii, or Turritopsis nutricula, is a small (5 millimeters (0.20 in)) species of jellyfish that uses transdifferentiation to replenish cells after sexual reproduction. This cycle can repeat indefinitely, potentially rendering it biologically immortal. This organism originated in the Caribbean Sea, but has now spread around the world.[citation needed] Key molecular mechanisms of its rejuvenation appear to involve DNA replication and repair, and stem cell renewal, according to a comparative genomics study.[20][21]

Similar cases include hydrozoan Laodicea undulata[22] and scyphozoan Aurelia sp.1.[23]

Lobsters

Further information: Lobster § Longevity

Research suggests that lobsters may not slow down, weaken, or lose fertility with age, and that older lobsters may be more fertile than younger lobsters. This does not however make them immortal in the traditional sense, as they are significantly more likely to die at a shell moult the older they get (as detailed below).

Their longevity may be due to telomerase, an enzyme that repairs long repetitive sections of DNA sequences at the ends of chromosomes, referred to as telomeres. Telomerase is expressed by most vertebrates during embryonic stages but is generally absent from adult stages of life.[24] However, unlike vertebrates, lobsters express telomerase as adults through most tissue, which has been suggested to be related to their longevity.[25][26][27] Contrary to popular belief, lobsters are not immortal. Lobsters grow by moulting, which requires considerable energy, and the larger the shell the more energy is required.[28] Eventually, the lobster will die from exhaustion during a moult. Older lobsters are also known to stop moulting, which means that the shell will eventually become damaged, infected, or fall apart, causing them to die.[29] The European lobster has an average life span of 31 years for males and 54 years for females.

Planarian flatworms

Polycelis felina, a freshwater planarian

Planarian flatworms have both sexually and asexually reproducing types. Studies on genus Schmidtea mediterranea suggest these planarians appear to regenerate (i.e. heal) indefinitely, and asexual individuals have an "apparently limitless [telomere] regenerative capacity fueled by a population of highly proliferative adult stem cells".[30]

For sexually reproducing planaria: "the lifespan of individual planarian can be as long as 3 years, likely due to the ability of neoblasts to constantly replace aging cells". Whereas for asexually reproducing planaria: "individual animals in clonal lines of some planarian species replicating by fission have been maintained for over 15 years".[31][32]

See also

References

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  2. ^ Michael R. Rose; Casandra L. Rauser; Laurence D. Mueller (Nov–Dec 2005). "Late life: a new frontier for physiology". Physiological and Biochemical Zoology. 78 (6): 869–878. doi:10.1086/498179. PMID 16228927. S2CID 31627493.
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  6. ^ Bulzomi, Pamela. "The Pro-apoptotic Effect of Quercetin in Cancer Cell Lines Requires ERβ-Dependant Signals." Cellular Physiology (2012): 1891-898. Web.
  7. ^ Reitzer, Lawrence J.; Wice, Burton M.; Kennel, David (1978), "Evidence That Glutamine, Not Sugar, Is the Major Energy Source for Cultured HeLa Cells", The Journal of Biological Chemistry, 254 (April 25): 26X9–2676, PMID 429309
  8. ^ University of Cologne (7 March 2018). "On the immortality of stem cells". ScienceDaily. Retrieved 17 September 2020.
  9. ^ Surani, Azim (1 April 2009). "Germ cells: the route to immortality". University of Cambridge. Retrieved 17 September 2020.
  10. ^ Michael R. Rose; Casandra L. Rauser; Laurence D. Mueller (1983). "Expression of the Large T Protein of Polyoma Virus Promotes the Establishment in Culture of "Normal" Rodent Fibroblast Cell Lines". PNAS. 80 (14): 4354–4358. Bibcode:1983PNAS...80.4354R. doi:10.1073/pnas.80.14.4354. PMC 384036. PMID 6308618.
  11. ^ Irfan Maqsood, M.; Matin, M. M.; Bahrami, A. R.; Ghasroldasht, M. M. (2013). "Immortality of cell lines: Challenges and advantages of establishment". Cell Biology International. 37 (10): 1038–45. doi:10.1002/cbin.10137. PMID 23723166. S2CID 14777249.
  12. ^ Species with Negligible Senescence Archived 2015-04-17 at the Wayback Machine. AnAge: The Animal Ageing and Longevity Database
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  16. ^ Current Biology: Volume 23, Issue 19, 7 October 2013, Pages 1844–1852 "Fission Yeast Does Not Age under Favorable Conditions, but Does So after Stress." Miguel Coelho1, 4, Aygül Dereli1, Anett Haese1, Sebastian Kühn2, Liliana Malinovska1, Morgan E. DeSantis3, James Shorter3, Simon Alberti1, Thilo Gross2, 5, Iva M. Tolić-Nørrelykke1
  17. ^ Bellantuono, Anthony J.; Bridge, Diane; Martínez, Daniel E. (2015-01-30). "Hydra as a tractable, long-lived model system for senescence". Invertebrate Reproduction & Development. 59 (sup1): 39–44. doi:10.1080/07924259.2014.938196. ISSN 0792-4259. PMC 4464093. PMID 26136619.
  18. ^ Buzgariu, Wanda; Wenger, Yvan; Tcaciuc, Nina; Catunda-Lemos, Ana-Paula; Galliot, Brigitte (2018-01-15). "Impact of cycling cells and cell cycle regulation on Hydra regeneration". Developmental Biology. 433 (2): 240–253. doi:10.1016/j.ydbio.2017.11.003. ISSN 0012-1606. PMID 29291976.
  19. ^ Martínez, Daniel E. (1998). "Mortality patterns suggest lack of senescence in Hydra" (PDF). Experimental Gerontology. 33 (3): 217–225. CiteSeerX 10.1.1.500.9508. doi:10.1016/S0531-5565(97)00113-7. PMID 9615920. S2CID 2009972. Archived (PDF) from the original on 2016-04-26.
  20. ^ Greenwood, Veronique (6 September 2022). "This Jellyfish Can Live Forever. Its Genes May Tell Us How". The New York Times. Retrieved 22 September 2022.
  21. ^ Pascual-Torner, Maria; Carrero, Dido; Pérez-Silva, José G.; Álvarez-Puente, Diana; Roiz-Valle, David; Bretones, Gabriel; Rodríguez, David; Maeso, Daniel; Mateo-González, Elena; Español, Yaiza; Mariño, Guillermo; Acuña, José Luis; Quesada, Víctor; López-Otín, Carlos (6 September 2022). "Comparative genomics of mortal and immortal cnidarians unveils novel keys behind rejuvenation". Proceedings of the National Academy of Sciences. 119 (36): e2118763119. Bibcode:2022PNAS..11918763P. doi:10.1073/pnas.2118763119. ISSN 0027-8424. PMC 9459311. PMID 36037356.
  22. ^ De Vito; et al. (2006). "Evidence of reverse development in Leptomedusae (Cnidaria, Hydrozoa): the case of Laodicea undulata (Forbes and Goodsir 1851)". Marine Biology. 149 (2): 339–346. doi:10.1007/s00227-005-0182-3. S2CID 84325535.
  23. ^ He; et al. (2015-12-21). "Life Cycle Reversal in Aurelia sp.1 (Cnidaria, Scyphozoa)". PLOS ONE. 10 (12): e0145314. Bibcode:2015PLoSO..1045314H. doi:10.1371/journal.pone.0145314. PMC 4687044. PMID 26690755.
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  25. ^ Wolfram Klapper; Karen Kühne; Kumud K. Singh; Klaus Heidorn; Reza Parwaresch & Guido Krupp (1998). "Longevity of lobsters is linked to ubiquitous telomerase expression". FEBS Letters. 439 (1–2): 143–146. doi:10.1016/S0014-5793(98)01357-X. PMID 9849895. S2CID 33161779.
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  28. ^ "Biotemp". Archived from the original on 2015-02-11. Retrieved 2015-02-10.
  29. ^ Koren, Marina. "Don't Listen to the Buzz: Lobsters Aren't Actually Immortal". Archived from the original on 2015-02-12.
  30. ^ Thomas C. J. Tan; Ruman Rahman; Farah Jaber-Hijazi; Daniel A. Felix; Chen Chen; Edward J. Louis & Aziz Aboobaker (February 2012). "Telomere maintenance and telomerase activity are differentially regulated in asexual and sexual worms". PNAS. 109 (9): 4209–4214. Bibcode:2012PNAS..109.4209T. doi:10.1073/pnas.1118885109. PMC 3306686. PMID 22371573. Archived from the original on 2012-03-06.
  31. ^ "Schmidtea , model planarian". www.geochembio.com. Archived from the original on 2010-12-30.
  32. ^ Archived at Ghostarchive and the Wayback Machine: "What Bodies Think About: Bioelectric Computation Outside the Nervous System - NeurIPS 2018". YouTube.

Bibliography

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