К книге
Старение. Почему эволюция убивает?Список литературы
100%
Список литературы
62

1. Lidsky P. V., Andino R. Epidemics as an adaptive driving force determining lifespan setpoints. Proceedings of the National Academy of Sciences. 2020; 117(30):17937–48.

2. Lidsky P. V., Andino R. Could aging evolve as a pathogen control strategy? Trends in Ecology Evolution. 2022; 37(12):1046–57.

3. Lidsky P. V., Yuan J., Rulison J. M., Andino-Pavlovsky R. Is aging an inevitable characteristic of organic life or an evolutionary adaptation? Biochemistry (Moscow). 2022; 87(12):1413–45.

4. Lidsky P. V., Yuan J., Andino R. Reconsidering life history theory amid infectious diseases. Trends in Ecology Evolution. 2023; 38(8):699–700.

5. Ramakrishnan V. Why We Die: The New Science of Aging and the Quest for Immortality 2024.

6. Cohen A. A., Kennedy B. K., Anglas U., Bronikowski A. M., Deelen J., Dufour F., et al. Lack of consensus on an aging biology paradigm? A global survey reveals an agreement to disagree, and the need for an interdisciplinary framework. Mech Ageing Dev. 2020;191:111316. Epub 20200718. doi: 10.1016/j. mad.2020.111316. PubMed PMID: 32693105; PubMed Central PMCID: PMCPMC7603428.

7. Gladyshev V. N., Anderson B., Barlit H., Barré B., Beck S., Behrouz B., et al. Disagreement on foundational principles of biological aging. PNAS nexus. 2024; 3(12): p. 499.

8. Piraino S., Boero F., Aeschbach B., Schmid V. Reversing the Life Cycle: Medusae Transforming into Polyps and Cell Transdifferentiation in Turritopsis nutricula (Cnidaria, Hydrozoa). The Biological Bulletin. 1996; 190(3):302−12. doi: 10.2307/1543022. PubMed PMID: 29227703.

9. Tomczyk S., Fischer K., Austad S., Galliot B. Hydra, a powerful model for aging studies. Invertebrate reproduction development. 2015; 59(sup1):11–6.

10. Sahu S., Dattani A., Aboobaker A. A., editors. Secrets from immortal worms: What can we learn about biological ageing from the planarian model system? Seminars in cell developmental biology; 2017: Elsevier.

11. Ruby J. G., Smith M., Buffenstein R. Naked mole-rat mortality rates defy Gompertzian laws by not increasing with age. elife. 2018; 7:e31157.

12. Braude S., Ciszek D. Survival of naked mole-rats marked by implantable transponders and toe-clipping. Journal of Mammalogy. 1998; 79(1):360–3.

13. Dias B. G., Ressler K. J. Parental olfactory experience influences behavior and neural structure in subsequent generations. Nat Neurosci. 2014; 17(1):89–96. Epub 20131201. doi: 10.1038/nn.3594. PubMed PMID: 24292232; PubMed Central PMCID: PMCPMC3923835.

14. Kroemer G., Maier A. B., Cuervo A. M., Gladyshev V. N., Ferrucci L., Gorbunova V., et al. From geroscience to precision geromedicine: Understanding and managing aging. Cell. 2025; 188(8):2043–62.

15. López-Otín C., Blasco M. A., Partridge L., Serrano M., Kroemer G. The hallmarks of aging. Cell. 2013; 153(6):1194–217.

16. López-Otín C., Blasco M. A., Partridge L., Serrano M., Kroemer G. Hallmarks of aging: An expanding universe. Cell. 2023; 186(2):243–78.

17. Kroemer G., Maier A. B., Cuervo A. M., Gladyshev V. N., Ferrucci L., Gorbunova V., et al. From geroscience to precision geromedicine: Understanding and managing aging. Cell. 2025; 188(8):2043–62. doi: 10.1016/j. cell.2025.03.011.

18. Gems D., de Magalhães J. P. The hoverfly and the wasp: A critique of the hallmarks of aging as a paradigm. Ageing Res Rev. 2021; 70:101407. Epub 20210713. doi: 10.1016/j. arr.2021.101407. PubMed PMID: 34271186; PubMed Central PMCID: PMCPMC7611451.

19. Magalhães J. Pd., Costa J., Church G. M. An analysis of the relationship between metabolism, developmental schedules, and longevity using phylogenetic independent contrasts. The Journals of Gerontology Series A: Biological Sciences and Medical Sciences. 2007; 62(2):149–60.

20. Vazquez J. M., Lauterbur M. E., Mottaghinia S., Bucci M., Fraser D., Gray-Sandoval G., et al. Extensive longevity and DNA virus-driven adaptation in nearctic Myotis bats. bioRxiv. 2024. Epub 20241127. doi: 10.1101/2024.10.10.617725. PubMed PMID: 39416019; PubMed Central PMCID: PMCPMC11482938.

21. Omotoso O., Gladyshev V. N., Zhou X. Lifespan extension in long-lived vertebrates rooted in ecological adaptation. Frontiers in Cell and Developmental Biology. 2021; 9:704966.

22. Reichard M., Polačik M. Nothobranchius furzeri, an «instant» fish from an ephemeral habitat. eLife. 2019; 8:e41548. doi: 10.7554/eLife.41548.

23. Li S., Vazquez J. M., Sudmant P. H. The evolution of aging and lifespan. Trends in Genetics. 2023; 39(11):830–43.

24. Deevey Jr. E. S. Life tables for natural populations of animals. The Quarterly Review of Biology. 1947; 22(4):283–314.

25. Jones O. R., Scheuerlein A., Salguero-Gómez R., Camarda C. G., Schaible R., Casper B. B., et al. Diversity of ageing across the tree of life. Nature. 2014; 505(7482):169–73.

26. Nussey D. H., Froy H., Lemaitre J.-F., Gaillard J.-M., Austad S. N. Senescence in natural populations of animals: widespread evidence and its implications for bio-gerontology. Ageing research reviews. 2013; 12(1):214–25.

27. Tidière M., Gaillard J.-M., Berger V., Müller D. W., Bingaman Lackey L., Gimenez O., et al. Comparative analyses of longevity and senescence reveal variable survival benefits of living in zoos across mammals. Scientific reports. 2016; 6(1):36361.

28. Wachter K. W., Evans S. N., Steinsaltz D. The age-specific force of natural selection and biodemographic walls of death. Proceedings of the National Academy of Sciences. 2013; 110(25):10141–6.

29. Penna T. J. A bit-string model for biological aging. arXiv preprint cond-mat/9503099. 1995.

30. Fernandes M., Wan C., Tacutu R., Barardo D., Rajput A., Wang J., et al. Systematic analysis of the gerontome reveals links between aging and age-related diseases. Human Molecular Genetics. 2016; 25(21):4804–18. doi: 10.1093/hmg/ddw307.

31. Skulachev V. P., Shilovsky G. A., Putyatina T. S., Popov N. A., Markov A. V., Skulachev M. V., et al. Perspectives of Homo sapiens lifespan extension: focus on external or internal resources? Aging (Albany NY). 2020; 12(6):5566.

32. Rose M. R., Charlesworth B. Genetics of life history in Drosophila melanogaster. II. Exploratory selection experiments. Genetics. 1981; 97(1):187–96.

33. Williams GC. PLEIOTROPY, NATURAL SELECTION, AND THE EVOLUTION OF SENESCENCE. Evolution. 1957;11(4):398–411. doi: https://doi.org/10.1111/j.1558–5646.1957.tb02911.x.

34. Leroi A. M., Chen W. R., Rose M. R. Long-term laboratory evolution of a genetic life-history trade-off in Drosophila melanogaster. 2. Stability of genetic correlations. Evolution. 1994; 48(4):1258–68.

35. Levine M. Live long prosper: evidence of evolutionary forces on lifespan. Nature Reviews Genetics. 2023; 24(2):72-.

36. Gems D., Kern C. Biological constraint, evolutionary spandrels and antagonistic pleiotropy. Ageing Research Reviews. 2024:1025–27.

37. Bartke A. Single-gene mutations and healthy ageing in mammals. Philosophical Transactions of the Royal Society B: Biological Sciences. 2011; 366(1561):28–34.

38. Yordy J., Kraus C., Hayward J. J., White M. E., Shannon L. M., Creevy K. E., et al. Body size, inbreeding, and lifespan in domestic dogs. Conservation genetics. 2020; 21:137–48.

39. Guevara-Aguirre J., Balasubramanian P., Guevara-Aguirre M., Wei M., Madia F., Cheng C.-W., et al. Growth hormone receptor deficiency is associated with a major reduction in pro-aging signaling, cancer, and diabetes in humans. Science translational medicine. 2011; 3(70):70ra13−70ra13.

40. Charlesworth B. Fisher, Medawar, Hamilton and the evolution of aging. Genetics. 2000; 156(3):927–31.

41. Kirkwood T. B. Evolution of ageing. Nature. 1977; 270(5635):301–4.

42. Voituron Y., de Fraipont M., Issartel J., Guillaume O., Clobert J. Extreme lifespan of the human fish (iProteus anguinus/i): a challenge for ageing mechanisms. Biology Letters. 2011; 7(1):105–7. doi: doi:10.1098/rsbl.2010.0539.

43. Ridgway I., Richardson C. Arctica islandica: the longest lived non colonial animal known to science. Reviews in Fish Biology and Fisheries. 2011; 21:297–310.

44. Nielsen J., Hedeholm R. B., Heinemeier J., Bushnell P. G., Christiansen J. S., Olsen J., et al. Eye lens radiocarbon reveals centuries of longevity in the Greenland shark (Somniosus microcephalus). Science. 2016; 353(6300):702–4.

45. Breed G. A., Vermeulen E., Corkeron P. Extreme longevity may be the rule not the exception in Balaenid whales. Science Advances. 2024; 10(51):eadq3086.

46. Shanley D. P., Kirkwood TBL. CALORIE RESTRICTION AND AGING: A LIFE-HISTORY ANALYSIS. Evolution. 2000; 54(3):740–50. doi: 10.1111/j.0014–3820.2000.tb00076.x.

47. Soto-Angel J. J., Burkhardt P. Reverse development in the ctenophore Mnemiopsis leidyi. Proceedings of the National Academy of Sciences. 2024; 121(45):e2411499121.

48. Korb J., Hartfelder K. Life history and development-a framework for understanding developmental plasticity in lower termites. Biological Reviews. 2008; 83(3):295–313.

49. Ghaninia M., Haight K., Berger S. L., Reinberg D., Zwiebel L. J., Ray A., et al. Chemosensory sensitivity reflects reproductive status in the ant Harpegnathos saltator. Scientific reports. 2017; 7(1):3732.

50. Münch D., Amdam G. V. The curious case of aging plasticity in honey bees. FEBS letters. 2010; 584(12):2496–503.

51. Dammann P., Šumbera R., Maßmann C., Scherag A., Burda H. Extended longevity of reproductives appears to be common in Fukomys mole-rats (Rodentia, Bathyergidae). PLoS One. 2011; 6(4):e18757.

52. Guan C., Barron A. B., He X. J., Wang Z. L., Yan W. Y., Zeng Z. J. A Comparison of Digital Gene Expression Profiling and Methyl DNA Immunoprecipitation as Methods for Gene Discovery in Honeybee (Apis mellifera) Behavioural Genomic Analyses. PLOS ONE. 2013; 8(9):e73628. doi: 10.1371/journal.pone.0073628.

53. Vijg J., Schumacher B., Abakir A., Antonov M., Bradley C., Cagan A., et al. Mitigating age-related somatic mutation burden. Trends in molecular medicine. 2023; 29(7):530–40.

54. Hamilton W. D. The genetic theory of social behavior. I and II. Journal of theoretical biology. 1964; 7:1–52.

55. Gross H. P., Wurtsbaugh W. A., Luecke C. The role of anadromous sockeye salmon in the nutrient loading and productivity of Redfish Lake, Idaho. Transactions of the American Fisheries Society. 1998; 127(1):1–18.

56. Healey M. Life history of chinook salmon (Oncorhynchus tshawytscha). Pacific salmon life histories. 1991:311–93.

57. Lennox R. J., Berntsen H. H., Garseth Å. H., Hinch S. G., Hindar K., Ugedal O., et al. Prospects for the future of pink salmon in three oceans: From the native Pacific to the novel Arctic and Atlantic. Fish and Fisheries. 2023; 24(5):759–76. doi: https://doi.org/10.1111/faf.12760.

58. Oakwood M., Bradley A. J., Cockburn A. Semelparity in a large marsupial. Proceedings of the Royal Society of London Series B: Biological Sciences. 2001;268(1465):407−11.

59. Albanese M. S., Ojeda R. A., Astié A. A. Delayed mortality of males in Thylamys bruchi, a semelparous marsupial from the Monte Desert, Argentina. Journal of Mammalogy. 2021; 102(1):258–69.

60. Keller L., Genoud M. Extraordinary lifespans in ants: a test of evolutionary theories of ageing. Nature. 1997; 389(6654):958–60.

61. Shephard A. M., Hund A. K., Snell-Rood E. C. Metabolic stress as a driver of life-history plasticity: flight promotes longevity and antioxidant production in monarch butterflies. Proceedings of the Royal Society B. 2023; 290(2008):20231616.

62. Zhang B., Jun H., Wu J., Liu J., Xu X. S. Olfactory perception of food abundance regulates dietary restriction-mediated longevity via a brain-to-gut signal. Nature aging. 2021; 1(3):255–68.

63. Alcedo J., Kenyon C. Regulation of emC. elegans/em Longevity by Specific Gustatory and Olfactory Neurons. Neuron. 2004; 41(1):45–55. doi: 10.1016/S0896–6273(03)00816-X.

64. Gendron C. M., Chakraborty T. S., Duran C., Dono T., Pletcher S. D. Ring neurons in the Drosophila central complex act as a rheostat for sensory modulation of aging. PLOS Biology. 2023; 21(6):e3002149. doi: 10.1371/journal.pbio.3002149.

65. Muyle A., Bachtrog D., Marais G. A. B., Turner J. M. A. Epigenetics drive the evolution of sex chromosomes in animals and plants. Philosophical Transactions of the Royal Society B: Biological Sciences. 2021; 376(1826):20200124. doi: doi:10.1098/rstb.2020.0124.

66. Flintham E. O., Yoshida T., Smith S., Pavlou H. J., Goodwin S. F., Carazo P., et al. Interactions between the sexual identity of the nervous system and the social environment mediate lifespan in iDrosophila melanogaster/i. Proceedings of the Royal Society B: Biological Sciences. 2018; 285(1892):20181450. doi: doi:10.1098/rspb.2018.1450.

67. Delanoue R., Clot C., Leray C., Pihl T., Hudry B. Y chromosome toxicity does not contribute to sex-specific differences in longevity. Nature Ecology Evolution. 2023; 7(8):1245−56. doi: 10.1038/s41559−023–02089−7.

68. Min K.-J., Lee C.-K., Park H.-N. The lifespan of Korean eunuchs. Current Biology. 2012; 22(18):R792-R3. doi: 10.1016/j. cub.2012.06.036.

69. Howe L. M. Current perspectives on the optimal age to spay/castrate dogs and cats. Veterinary Medicine: Research and Reports. 2015; 6(null):171−80. doi: 10.2147/VMRR.S53264.

70. Tyshkovskiy A., Bozaykut P., Borodinova A. A., Gerashchenko M. V., Ables G. P., Garratt M., et al. Identification and Application of Gene Expression Signatures Associated with Lifespan Extension. Cell Metab. 2019; 30(3):573−93.e8. Epub 20190725. doi: 10.1016/j. cmet.2019.06.018. PubMed PMID: 31353263; PubMed Central PMCID: PMCPMC6907080.

71. Healy K., Guillerme T., Finlay S., Kane A., Kelly S. B., McClean D., et al. Ecology and mode-of-life explain lifespan variation in birds and mammals. Proceedings of the Royal Society B: Biological Sciences. 2014; 281(1784):20140298.

72. Bartke A. Somatic growth, aging, and longevity. npj Aging and Mechanisms of Disease. 2017; 3(1):14. doi: 10.1038/s41514−017−0014-y.

73. Gladyshev V. N. On the cause of aging and control of lifespan: heterogeneity leads to inevitable damage accumulation, causing aging; control of damage composition and rate of accumulation define lifespan. Bioessays. 2012; 34(11):925−9. Epub 20120823. doi: 10.1002/bies.201200092. PubMed PMID: 22915358; PubMed Central PMCID: PMCPMC3804916.

74. Healy K., Ezard T. H., Jones O. R., Salguero-Gómez R., Buckley Y. M. Animal life history is shaped by the pace of life and the distribution of age-specific mortality and reproduction. Nature ecology evolution. 2019; 3(8):1217–24.

75. Chapman T., Liddle L. F., Kalb J. M., Wolfner M. F., Partridge L. Cost of mating in Drosophila melanogaster females is mediated by male accessory gland products. Nature. 1995; 373(6511):241−4. doi: 10.1038/373241a0.

76. Kubli E., Bopp D. Sexual Behavior: How Sex Peptide Flips the Postmating Switch of Female Flies. Current Biology. 2012; 22(13):R520-R2. doi: https://doi.org/10.1016/j. cub.2012.04.058.

77. Harvanek Z. M., Lyu Y., Gendron C. M., Johnson J. C., Kondo S., Promislow D. E. L., et al. Perceptive costs of reproduction drive ageing and physiology in male Drosophila. Nature Ecology Evolution. 2017; 1(6):0152. doi: 10.1038/s41559−017–0152.

78. Westendorp R. G., Kirkwood T. B. Human longevity at the cost of reproductive success. Nature. 1998; 396(6713):743−6. doi: 10.1038/25519. PubMed PMID: 9874369.

79. Gavrilov L. A., Gavrilova N. S. Is There a Reproductive Cost for Human Longevity? Journal of Anti-Aging Medicine. 1999; 2(2):121−3. doi: 10.1089/rej.1.1999.2.121.

80. Mitchell S. E., Simpson M., Coulet L., Gouedard S., Hambly C., Morimoto J., et al. Reproduction has immediate effects on female mortality, but no discernible lasting physiological impacts: A test of the disposable soma theory. Proceedings of the National Academy of Sciences. 2024; 121(42):e2408682121.

81. Bower J. R., Noro K., Sakurai Y., Scheel D. Chapter 21 — Enteroctopus dofleini, Giant Pacific octopus. In: Rosa R, Gleadall IG, Pierce GJ, Villanueva R, editors. Octopus Biology and Ecology: Academic Press; 2024. p. 369–95.

82. Podlutsky A. J., Khritankov A. M., Ovodov N. D., Austad S. N. A new field record for bat longevity. J Gerontol A Biol Sci Med Sci. 2005; 60(11):1366−8. doi: 10.1093/gerona/60.11.1366. PubMed PMID: 16339320.

83. Wilkinson G. S., Adams D. M. Recurrent evolution of extreme longevity in bats. Biology letters. 2019; 15(4):20180860.

84. Geiser F., Stawski C. Hibernation and Torpor in Tropical and Subtropical Bats in Relation to Energetics, Extinctions, and the Evolution of Endothermy. Integrative and Comparative Biology. 2011; 51(3):337–48. doi: 10.1093/icb/icr042.

85. Austad S. N., Finch C. E. How ubiquitous is aging in vertebrates? Science. 2022; 376(6600):1384–5. doi: doi:10.1126/science.adc9442.

86. Wensink M. J., Caswell H., Baudisch A. The Rarity of Survival to Old Age Does Not Drive the Evolution of Senescence. Evol Biol. 2017; 44(1):5–10. Epub 20160504. doi: 10.1007/s11692−016–9385−4. PubMed PMID: 28280278; PubMed Central PMCID: PMCPMC5321711.

87. Moorad J., Promislow D., Silvertown J. Evolutionary Ecology of Senescence and a Reassessment of Williams' «Extrinsic Mortality» Hypothesis. Trends in Ecology Evolution. 2019;34(6):519−30. doi: https://doi.org/10.1016/j. tree.2019.02.006.

88. Reznick D. N., Bryant M. J., Roff D., Ghalambor C. K., Ghalambor D. E. Effect of extrinsic mortality on the evolution of senescence in guppies. Nature. 2004; 431(7012):1095−9. doi: 10.1038/nature02936.

89. Chen H. Y., Maklakov A. A. Longer life span evolves under high rates of condition-dependent mortality. Curr Biol. 2012; 22(22):2140–3. Epub 20121018. doi: 10.1016/j. cub.2012.09.021. PubMed PMID: 23084993.

90. Austad S. N. Retarded senescence in an insular population of Virginia opossums (Didelphis virginiana). Journal of Zoology. 1993; 229(4):695–708. doi: https://doi.org/10.1111/j.1469–7998.1993.tb02665.x.

91. de Vries C., Galipaud M., Kokko H. Extrinsic mortality and senescence: a guide for the perplexed. Peer Community Journal. 2023; 3.

92. Sandercock B. K., Jaramillo A. Annual Survival Rates of Wintering Sparrows: Assessing Demographic Consequences of Migration. The Auk. 2002; 119(1):149–65. doi: 10.1093/auk/119.1.149.

93. Pinho G. M., Martin J. G. A., Farrell C., Haghani A., Zoller J. A., Zhang J., et al. Hibernation slows epigenetic ageing in yellow-bellied marmots. Nature Ecology Evolution. 2022;6(4):418–26. doi: 10.1038/s41559−022–01679−1.

94. Turbill C., Bieber C., Ruf T. Hibernation is associated with increased survival and the evolution of slow life histories among mammals. Proceedings of the Royal Society B: Biological Sciences. 2011; 278(1723):3355−63. doi: doi:10.1098/rspb.2011.0190.

95. Wikipedia. Brandt’s bat (Myotis brandtii) 2025.

96. Funakoshi K. The longest life span based on the re-occupation record of Murina ussuriensis. Nature of Kagoshima. 2020; 47:47–39.

97. Kerepesi C., Meer M. V., Ablaeva J., Amoroso V. G., Lee S.-G., Zhang B., et al. Epigenetic aging of the demographically non-aging naked mole-rat. Nature Communications. 2022; 13(1):355. doi: 10.1038/s41467−022–27959−9.

98. Braude S. The behavior and demographics of the naked mole-rat, Heterocephalus glaber [Ph. D.]. United States — Michigan: University of Michigan; 1991.

99. Kerr P. J., Liu J., Cattadori I., Ghedin E., Read A. F., Holmes E. C. Myxoma Virus and the Leporipoxviruses: An Evolutionary Paradigm. Viruses [Internet]. 2015; 7(3):[1020−61 pp.].

100. Anderson R. M., May R. M. Coevolution of hosts and parasites. Parasitology. 1982; 85(2):411−26. Epub 2009/04/06. doi: 10.1017/S0031182000055360.

101. Enard D., Cai L., Gwennap C., Petrov D. A. Viruses are a dominant driver of protein adaptation in mammals. eLife. 2016; 5:e12469. doi: 10.7554/eLife.12469.

102. Halvorsen O., Andersen K. The ecological interaction between arctic charr, Salvelinus alpinus (L.), and the plerocercoid stage of Diphyllobothrium ditremum. Journal of Fish Biology. 1984; 25(3):305–16. doi: https://doi.org/10.1111/j.1095–8649.1984.tb04878.x.

103. Lachish S., Miller K. J., Storfer A., Goldizen A. W., Jones M. E. Evidence that disease-induced population decline changes genetic structure and alters dispersal patterns in the Tasmanian devil. Heredity. 2011; 106(1):172–82. doi: 10.1038/hdy.2010.17.

104. Miller M. B., Bassler B. L. Quorum Sensing in Bacteria. Annual Review of Microbiology. 2001; 55(Volume 55, 2001):165–99. doi: https://doi.org/10.1146/annurev.micro.55.1.165.

105. Matthysen E. Density-dependent dispersal in birds and mammals. Ecography. 2005; 28(3):403–16. doi: https://doi.org/10.1111/j.0906–7590.2005.04073.x.

106. Lopatina A., Tal N., Sorek R. Abortive Infection: Bacterial Suicide as an Antiviral Immune Strategy. Annu Rev Virol. 2020; 7(1):371–84. Epub 20200619. doi: 10.1146/annurev-virology-011620–040628. PubMed PMID: 32559405.

107. Beros S., Lenhart A., Scharf I., Negroni M. A., Menzel F., Foitzik S. Extreme lifespan extension in tapeworm-infected ant workers. Royal Society Open Science. 2021; 8(5):202118. doi: doi:10.1098/rsos.202118.

108. Beani L., Dallai R., Cappa F., Manfredini F., Zaccaroni M., Lorenzi M. C., et al. A Strepsipteran parasite extends the lifespan of workers in a social wasp. Scientific Reports. 2021; 11(1):7235. doi: 10.1038/s41598−021–86182–6.

109. Azevedo Jd. S., Silva L. Gd., Bizerri C. R. S. F, Dansa-Petretski M. A., Lima N. R. W. Infestation pattern and parasitic castration of the crustacean Riggia paranensis (Crustacea: Cymothoidea) on the fresh water fish Cyphocharax gilbert (Teleostei: Curimatidae). Neotropical Ichthyology. 2006; 4.

110. Hurd H., Warr E., Polwart A. A parasite that increases host lifespan. Proceedings of the Royal Society of London Series B: Biological Sciences. 2001; 268(1477):1749–53. doi: doi:10.1098/rspb.2001.1729.

111. Minchella D. J., Leathers B. K., Brown K. M., McNair J. N. Host and Parasite Counteradaptations: An Example from a Freshwater Snail. The American Naturalist. 1985; 126(6):843−54. doi: 10.1086/284456.

112. Libert S., Chao Y., Chu X., Pletcher S. D. Trade-offs between longevity and pathogen resistance in Drosophila melanogaster are mediated by NFkappaB signaling. Aging Cell. 2006; 5(6):533–43. doi: 10.1111/j.1474–9726.2006.00251.x. PubMed PMID: 17129215.

113. Tomusiak A., Floro A., Tiwari R., Riley R., Matsui H., Andrews N., et al. Development of an epigenetic clock resistant to changes in immune cell composition. Communications Biology. 2024; 7(1):934. doi: 10.1038/s42003−024–06609−4.

114. Gindin Y., Gaggar A., Lok A. S., Janssen H. L. A., Ferrari C., Subramanian G. M., et al. DNA Methylation and Immune Cell Markers Demonstrate Evidence of Accelerated Aging in Patients with Chronic Hepatitis B Virus or Hepatitis C Virus, with or without Human Immunodeficienct Virus Co-infection. Clin Infect Dis. 2021; 73(1):e184-e90. doi: 10.1093/cid/ciaa1371. PubMed PMID: 32915202; PubMed Central PMCID: PMCPMC8427715.

115. Ferrucci L., Fabbri E. Inflammageing: chronic inflammation in ageing, cardiovascular disease, and frailty. Nature Reviews Cardiology. 2018; 15(9):505–22. doi: 10.1038/s41569−018−0064−2.

116. Furman D., Campisi J., Verdin E., Carrera-Bastos P., Targ S., Franceschi C., et al. Chronic inflammation in the etiology of disease across the life span. Nat Med. 2019; 25(12):1822–32. Epub 20191205. doi: 10.1038/s41591−019–0675−0. PubMed PMID: 31806905; PubMed Central PMCID: PMCPMC7147972.

117. Ohnishi K., Semi K., Yamamoto T., Shimizu M., Tanaka A., Mitsunaga K., et al. Premature Termination of Reprogramming In Vivo Leads to Cancer Development through Altered Epigenetic Regulation. Cell. 2014; 156(4):663−77. doi: https://doi.org/10.1016/j. cell.2014.01.005.

118. Altenberg L. Evolvability suppression to stabilize far-sighted adaptations. Artif Life. 2005; 11(4):427–43. doi: 10.1162/106454605774270633. PubMed PMID: 16197672.

119. Zaba B., Gregson S. Measuring the impact of HIV on fertility in Africa. Aids. 1998; 12 Suppl 1:S41–50. PubMed PMID: 9677188.

120. Schulz K. F., Cates W. Jr., O’Mara P. R. Pregnancy loss, infant death, and suffering: legacy of syphilis and gonorrhoea in Africa. Genitourin Med. 1987; 63(5):320−5. doi: 10.1136/sti.63.5.320. PubMed PMID: 3679218; PubMed Central PMCID: PMCPMC1194101.

121. Berec L., Maxin D. Fatal or harmless: extreme bistability induced by sterilizing, sexually transmitted pathogens. Bull Math Biol. 2013; 75(2):258–73. Epub 20130105. doi: 10.1007/s11538−012–9802–5. PubMed PMID: 23292362.

122. Sharp P. M., Hahn B. H. Origins of HIV and the AIDS pandemic. Cold Spring Harb Perspect Med. 2011; 1(1):a006841. doi: 10.1101/cshperspect.a006841. PubMed PMID: 22229120; PubMed Central PMCID: PMCPMC3234451.

123. Xu R., Ekiert D. C., Krause J. C., Hai R., Crowe J. E., Wilson I. A. Structural Basis of Preexisting Immunity to the 2009 H1N1 Pandemic Influenza Virus. Science. 2010; 328(5976):357–60. doi: doi:10.1126/science.1186430.

124. Sutherland G. D., Harestad A. S., Price K., Lertzman K. P. Scaling of Natal Dispersal Distances in Terrestrial Birds and Mammals. Conservation Ecology. 2000; 4(1).

125. Hoyt J. R., Kilpatrick A. M., Langwig K. E. Ecology and impacts of white-nose syndrome on bats. Nature Reviews Microbiology. 2021; 19(3):196–210. doi: 10.1038/s41579−020–00493–5.

126. Wilkinson G. S. Reciprocal food sharing in the vampire bat. Nature. 1984; 308(5955):181−4. doi: 10.1038/308181a0.

127. Grant P. Evolution on Islands1997.

128. Lafferty K. D., Kuris A. M. Parasitic castration: the evolution and ecology of body snatchers. Trends in Parasitology. 2009; 25(12):564–72. doi: 10.1016/j. pt.2009.09.003.

129. Hamilton D. G., Jones M. E., Cameron E. Z., McCallum H., Storfer A., Hohenlohe P. A., et al. Rate of intersexual interactions affects injury likelihood in Tasmanian devil contact networks. Behavioral Ecology. 2019; 30(4):1087–95. doi: 10.1093/beheco/arz054.

130. Jones M. E., Cockburn A., Hamede R., Hawkins C., Hesterman H., Lachish S., et al. Life-history change in disease-ravaged Tasmanian devil populations. Proceedings of the National Academy of Sciences. 2008; 105(29):10023−7. doi: doi:10.1073/pnas.0711236105.

131. Stadtmauer D. J., Wagner G. P. Cooperative inflammation: The recruitment of inflammatory signaling in marsupial and eutherian pregnancy. J Reprod Immunol. 2020; 137:102626. Epub 20191025. doi: 10.1016/j. jri.2019.102626. PubMed PMID: 31783286; PubMed Central PMCID: PMCPMC7028515.

132. Stone W. H., Brunn D. A., Foster E. B., Manis G. S., Hoffman E. S., Saphire D. G., et al. Absence of a significant mixed lymphocyte reaction in a marsupial (Monodelphis domestica). Lab Anim Sci. 1998; 48(2):184–9. PubMed PMID: 10090011.

133. Artwohl J., Ball-Kell S., Valyi-Nagy T., Wilson S. P., Lu Y., Park T. J. Extreme susceptibility of African naked mole rats (Heterocephalus glaber) to experimental infection with herpes simplex virus type 1. Comp Med. 2009; 59(1):83–90. PubMed PMID: 19295058; PubMed Central PMCID: PMCPMC2703134.

134. Ross-Gillespie A., O’Riain M. J., Keller L. F. Viral epizootic reveals inbreeding depression in a habitually inbreeding mammal. Evolution. 2007; 61(9):2268–73. doi: 10.1111/j.1558–5646.2007.00177.x. PubMed PMID: 17767596; PubMed Central PMCID: PMCPMC7202238.

135. Hilton H. G., Rubinstein N. D., Janki P., Ireland A. T., Bernstein N., Fong N. L., et al. Single-cell transcriptomics of the naked mole-rat reveals unexpected features of mammalian immunity. PLOS Biology. 2019; 17(11):e3000528. doi: 10.1371/journal.pbio.3000528.

136. Pagel M., Bodmer W. A naked ape would have fewer parasites. Proc Biol Sci. 2003; 270 Suppl 1(Suppl 1):S117−9. doi: 10.1098/rsbl.2003.0041. PubMed PMID: 12952654; PubMed Central PMCID: PMCPMC1698033.

137. Müller D. W., Lackey L. B., Streich W. J., Fickel J., Hatt J. M., Clauss M. Mating system, feeding type and ex situ conservation effort determine life expectancy in captive ruminants. Proc Biol Sci. 2011; 278(1714):2076–80. Epub 20101208. doi: 10.1098/rspb.2010.2275. PubMed PMID: 21147792; PubMed Central PMCID: PMCPMC3107652.

138. Koski W. R., George J. C., Würsig B. Bowhead Whale Reproductive Strategies. In: Würsig B, Orbach DN, editors. Sex in Cetaceans: Morphology, Behavior, and the Evolution of Sexual Strategies. Cham: Springer International Publishing; 2023. p. 521–41.

139. Watkins A. Reevaluating the grandmother hypothesis. History and Philosophy of the Life Sciences. 2021; 43(3):103. doi: 10.1007/s40656−021–00455-x.

140. Nakagawa S., Lagisz M., Hector K. L., Spencer H. G. Comparative and meta-analytic insights into life extension via dietary restriction. Aging Cell. 2012; 11(3):401–9. doi: https://doi.org/10.1111/j.1474–9726.2012.00798.x.

141. Halverson M. S., Bolnick D. A. An ancient DNA test of a founder effect in Native American ABO blood group frequencies. Am J Phys Anthropol. 2008; 137(3):342–7. doi: 10.1002/ajpa.20887. PubMed PMID: 18618657.

142. Ludwig F. C., Elashoff R. M. Mortality in syngeneic rat parabionts of different chronological age. Trans N Y Acad Sci. 1972; 34(7):582–7. doi: 10.1111/j.2164−0947.1972.tb02712.x. PubMed PMID: 4507935.

143. Butenko G. M., Gubrii I. B. Inhibition of the immune responses of young adult CBA mice due to parabiosis with their old partners. Experimental Gerontology. 1980; 15(6):605–10. doi: https://doi.org/10.1016/0531–5565(80)90012−1.

144. Conboy I. M., Conboy M. J., Wagers A. J., Girma E. R., Weissman I. L., Rando T. A. Rejuvenation of aged progenitor cells by exposure to a young systemic environment. Nature. 2005; 433(7027):760–4. doi: 10.1038/nature03260.

145. Mehdipour M., Skinner C., Wong N., Lieb M., Liu C., Etienne J., et al. Rejuvenation of three germ layers tissues by exchanging old blood plasma with saline-albumin. Aging (Albany NY). 2020; 12(10):8790–819. Epub 20200530. doi: 10.18632/aging.103418. PubMed PMID: 32474458; PubMed Central PMCID: PMCPMC7288913.

146. Heavener K. S., Bradshaw E. M. The aging immune system in Alzheimer’s and Parkinson’s diseases. Semin Immunopathol. 2022; 44(5):649−57. Epub 20220503. doi: 10.1007/s00281−022–00944–6. PubMed PMID: 35505128; PubMed Central PMCID: PMCPMC9519729.

147. Molony R. D., Nguyen J. T., Kong Y., Montgomery R. R., Shaw A. C., Iwasaki A. Aging impairs both primary and secondary RIG-I signaling for interferon induction in human monocytes. Sci Signal. 2017; 10(509). Epub 20171212. doi: 10.1126/scisignal.aan2392. PubMed PMID: 29233916; PubMed Central PMCID: PMCPMC6429941.

148. Flores R. R., Clauson C. L., Cho J., Lee B. C., McGowan S. J., Baker D. J., et al. Expansion of myeloid-derived suppressor cells with aging in the bone marrow of mice through a NF-kB-dependent mechanism. Aging Cell. 2017; 16(3):480–7. Epub 20170223. doi: 10.1111/acel.12571. PubMed PMID: 28229533; PubMed Central PMCID: PMCPMC5418207.

149. Yousefzadeh M. J., Flores R. R., Zhu Y, Schmiechen Z. C., Brooks R. W., Trussoni C. E., et al. An aged immune system drives senescence and ageing of solid organs. Nature. 2021; 594(7861):100–5. Epub 20210512. doi: 10.1038/s41586−021–03547−7. PubMed PMID: 33981041; PubMed Central PMCID: PMCPMC8684299.

150. Hayflick L., Moorhead p.s. The serial cultivation of human diploid cell strains. Experimental Cell Research. 1961; 25(3):585–621. doi: https://doi.org/10.1016/0014–4827(61)90192−6.

151. Huang W., Hickson L. J., Eirin A., Kirkland J. L., Lerman L. O. Cellular senescence: the good, the bad and the unknown. Nature Reviews Nephrology. 2022; 18(10):611–27. doi: 10.1038/s41581−022–00601-z.

152. Schmitt C. A., Wang B., Demaria M. Senescence and cancer — role and therapeutic opportunities. Nat Rev Clin Oncol. 2022; 19(10):619–36. Epub 20220831. doi: 10.1038/s41571−022–00668−4. PubMed PMID: 36045302; PubMed Central PMCID: PMCPMC9428886.

153. Kowald A., Kirkwood T. B. L. Senolytics and the compression of late-life mortality. Exp Gerontol. 2021; 155:111588. Epub 20211009. doi: 10.1016/j. exger.2021.111588. PubMed PMID: 34637949.

154. Muñoz-Espín D., Cañamero M., Maraver A., Gómez-López G., Contreras J., Murillo-Cuesta S., et al. Programmed cell senescence during mammalian embryonic development. Cell. 2013; 155(5):1104–18. Epub 20131114. doi: 10.1016/j. cell.2013.10.019. PubMed PMID: 24238962.

155. Dworak H., Rozmaric T., Grillari J., Ogrodnik M. Cells of all trades — on the importance of spatial positioning of senescent cells in development, healing and aging. FEBS Letters. 2025;n/a(n/a). doi: https://doi.org/10.1002/1873–3468.70037.

156. Lee S., Yu Y., Trimpert J., Benthani F., Mairhofer M., Richter-Pechanska P., et al. Virus-induced senescence is a driver and therapeutic target in COVID-19. Nature. 2021; 599(7884):283–9. doi: 10.1038/s41586−021–03995−1.

157. Karakousis N. D., Papatheodoridi A., Chatzigeorgiou A., Papatheodoridis G. Cellular senescence and hepatitis B-related hepatocellular carcinoma: An intriguing link. Liver Int. 2020; 40(12):2917–27. doi: 10.1111/liv.14659. PubMed PMID: 32890439.

158. Baz-Martínez M., Da Silva-Álvarez S., Rodríguez E., Guerra J., El Motiam A., Vidal A., et al. Cell senescence is an antiviral defense mechanism. Scientific Reports. 2016; 6(1):37007. doi: 10.1038/srep37007.

159. Miller K. N., Victorelli S. G., Salmonowicz H., Dasgupta N., Liu T., Passos J. F., et al. Cytoplasmic DNA: sources, sensing, and role in aging and disease. Cell. 2021; 184(22):5506–26. doi: 10.1016/j. cell.2021.09.034. PubMed PMID: 34715021; PubMed Central PMCID: PMCPMC8627867.

160. Camell C. D., Yousefzadeh M. J., Zhu Y., Prata L., Huggins M. A., Pierson M., et al. Senolytics reduce coronavirus-related mortality in old mice. Science. 2021; 373(6552). Epub 20210608. doi: 10.1126/science.abe4832. PubMed PMID: 34103349; PubMed Central PMCID: PMCPMC8607935.

161. Lee K. A., Flores R. R., Jang I. H., Saathoff A., Robbins P. D. Immune Senescence, Immunosenescence and Aging. Front Aging. 2022; 3:900028. Epub 20220530. doi: 10.3389/fragi.2022.900028. PubMed PMID: 35821850; PubMed Central PMCID: PMCPMC9261375.

162. Wu L. E., Fiveash C. E., Bentley N. L., Kang M. J., Govindaraju H., Barbour J. A., et al. SIRT2 transgenic over-expression does not impact lifespan in mice. Aging Cell. 2023; 22(12):e14027. Epub 20231127. doi: 10.1111/acel.14027. PubMed PMID: 38009412; PubMed Central PMCID: PMCPMC10726910.

163. Kaeberlein M., Creevy K. E., Promislow D. E. The dog aging project: translational geroscience in companion animals. Mamm Genome. 2016; 27(7–8):279–88. Epub 20160503. doi: 10.1007/s00335−016–9638−7. PubMed PMID: 27143112; PubMed Central PMCID: PMCPMC4936929.

164. Dorman J. B., Albinder B., Shroyer T., Kenyon C. The age-1 and daf-2 genes function in a common pathway to control the lifespan of Caenorhabditis elegans. Genetics. 1995; 141(4):1399–406. doi: 10.1093/genetics/141.4.1399. PubMed PMID: 8601482; PubMed Central PMCID: PMCPMC1206875.

165. He Q., Morris B. J., Grove J. S., Petrovitch H., Ross W., Masaki K. H., et al. Shorter men live longer: association of height with longevity and FOXO3 genotype in American men of Japanese ancestry. PLoS One. 2014; 9(5):e94385. Epub 20140507. doi: 10.1371/journal.pone.0094385. PubMed PMID: 24804734; PubMed Central PMCID: PMCPMC4013008.

166. McGaugh S. E., Bronikowski A. M., Kuo C.-H., Reding D. M., Addis E. A., Flagel L. E., et al. Rapid molecular evolution across amniotes of the IIS/TOR network. Proceedings of the National Academy of Sciences. 2015; 112(22):7055–60. doi: 10.1073/pnas.1419659112.

Предыдущая главаГлава 62 из 62К книге