Longevity, stress response, and cancer in aging telomerase-deficient mice

Karl Lenhard Rudolph, Sandy Chang, Han Woong Lee, Maria Blasco, Geoffrey J. Gottlieb, Carol W Greider, Ronald A. DePinho

Research output: Contribution to journalArticle

Abstract

Telomere maintenance is thought to play a role in signaling cellular senescence; however, a link with organismal aging processes has not been established. The telomerase null mouse provides an opportunity to understand the effects associated with critical telomere shortening at the organismal level. We studied a variety of physiological processes in an aging cohort of mTR(-/-) mice. Loss of telomere function did not elicit a full spectrum of classical pathophysiological symptoms of aging. However, age-dependent telomere shortening and accompanying genetic instability were associated with shortened life span as well as a reduced capacity to respond to stresses such as wound healing and hematopoietic ablation. In addition, we found an increased incidence of spontaneous malignancies. These findings demonstrate a critical role for telomere length in the overall fitness, reserve, and well being of the aging organism.

Original languageEnglish (US)
Pages (from-to)701-712
Number of pages12
JournalCell
Volume96
Issue number5
StatePublished - Mar 5 1999

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ASJC Scopus subject areas

  • Cell Biology
  • Molecular Biology

Cite this

Rudolph, K. L., Chang, S., Lee, H. W., Blasco, M., Gottlieb, G. J., Greider, C. W., & DePinho, R. A. (1999). Longevity, stress response, and cancer in aging telomerase-deficient mice. Cell, 96(5), 701-712.