Experimental Hematology
Volume 30, Issue 10 , Pages 1147-1152, October 2002

Longitudinal studies of telomere length in feline blood cells:

Implications for hematopoietic stem cell turnover in vivo

  • Tim H Brümmendorf

      Affiliations

    • Terry Fox Laboratory, BC Cancer Agency, Vancouver, BC, Canada
    • Department of Hematology and Oncology, University Medical Center II, Tübingen, Germany
  • ,
  • Jennifer Mak

      Affiliations

    • Terry Fox Laboratory, BC Cancer Agency, Vancouver, BC, Canada
  • ,
  • Kathleen M Sabo

      Affiliations

    • Division of Hematology, Department of Medicine, University of Washington, Seattle, Wash., USA
  • ,
  • Gabriela M Baerlocher

      Affiliations

    • Terry Fox Laboratory, BC Cancer Agency, Vancouver, BC, Canada
  • ,
  • Klaus Dietz

      Affiliations

    • Department of Medical Biometry, University of Tübingen, Tübingen, Germany
  • ,
  • Janis L Abkowitz

      Affiliations

    • Division of Hematology, Department of Medicine, University of Washington, Seattle, Wash., USA
  • ,
  • Peter M Lansdorp

      Affiliations

    • Corresponding Author InformationOffprint requests to: Peter M. Lansdorp, M.D., Ph.D., Terry Fox Laboratory, BC Cancer Agency, 601 West 10th Avenue, Vancouver, BC, V5Z 1L3, Canada
    • Terry Fox Laboratory, BC Cancer Agency, Vancouver, BC, Canada
    • Department of Medicine, University of BC, Vancouver, BC, Canada

Received 10 April 2002; received in revised form 21 May 2002; accepted 28 May 2002.

Abstract 

Objective

To address questions about stem cell turnover in relation to telomere length dynamics, we analyzed telomere length in serial blood samples from cats.

Materials and Methods

Lymphocytes and granulocytes from two newborn kittens, a 2-year-old cat, a 10-year-old recipient of a double autologous stem cell transplant, and a 10-year-old control animal were analyzed by fluorescence in situ hybridization and flow cytometry at 2-week intervals over a 1-year period.

Results

At study onset, long telomeres were found in granulocytes and lymphocytes from the two kittens (mean ± SD: 70.2 ± 3.1 and 72.5 ± 3.1 telomere fluorescence units [TFU], respectively) compared with the 2-year-old cat (55.6 ± 2.5 and 64.1 ± 4.3 TFU, respectively) and the two adult animals (49.6 ± 1.5 and 45.4 ± 0.8 TFU, respectively). The rate of telomere shortening in both granulocytes and lymphocytes was most rapid in the kittens (slope: −16.7 ± 1.4 and −15.6 ± 0.2 TFU/year, respectively). As in humans, telomere shortening with age was more rapid in lymphocytes than in granulocytes. An average rate of telomere attrition of −0.52 ± 0.03 TFU per cell division was calculated for cultured lymphocytes from the two kittens, approximately 5-fold higher than the rate observed in human cells.

Conclusions

The average telomere length in cats is 5- to 10-fold longer than in humans, but the rate of telomere shortening is much higher both in vivo and in vitro. These observations are compatible with similar stem cell kinetics in both species.

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PII: S0301-472X(02)00888-3

Experimental Hematology
Volume 30, Issue 10 , Pages 1147-1152, October 2002