4.7 Article

Telomere dynamics in Macaques and humans

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/gerona/62.4.367

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Funding

  1. NCI NIH HHS [CA75907, R15 CA132090] Funding Source: Medline
  2. NIA NIH HHS [R21 AG041375, AG020132, AG021593] Funding Source: Medline
  3. NIGMS NIH HHS [R15 GM099008, F32 GM067522] Funding Source: Medline

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In humans, telomere length in proliferating tissues shortens with age-a process accelerated with age-related diseases. Thus, telomere length and attrition with age in the nonhuman primate may serve as a useful paradigm for understanding telomere biology in humans. We examined telomere parameters in tissues of young and old Macaca fascicularis and compared them with several tissues from humans. Macaque telomeres were variable in length and exhibited partial synchrony (equivalence) within animals. They were longer than humans, partially because of longer subtelomeric segments. As skeletal muscle telomere length was unchanged with age, we used it as an internal reference to offset interanimal variation in telomere length. We identified age-dependent telomere attrition in lung, pancreas, skin, and thyroid. Similar to humans, telomerase activity was detected in spleen, thymus, digestive tract, and gonads. We conclude that factors that modify telomere attrition and aging in humans may also operate in the macaque.

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