|
|
Blood, 15 September 2007, Vol. 110, No. 6, pp. 1806-1813.
Prepublished online as a Blood First Edition Paper on May 25, 2007; DOI 10.1182/blood-2007-02-075382.
Previous Article | Next Article 
Submitted February 20, 2007
Accepted May 9, 2007
Hematopoietic stem cell behavior in non-human primates
Bryan E Shepherd, Hans-Peter Kiem, Peter M Lansdorp, Cynthia E Dunbar, Geraldine Aubert, Andre LaRochelle, Ruth Seggewiss, Peter Guttorp, and Janis L. Abkowitz*
Department of Biostatistics, Vanderbilt University, Nashville, TN, United States
Department of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, WA, United States
Terry Fox Laboratory, University of British Columbia, Vancouver, Canada
NHLBI, NIH, Bethesda, MD, United States
Department of Statistics, University of Washington, Seattle, WA, United States
Division of Hematology/Medicine, University of Washington, Seattle, WA, United States
* Corresponding author; email: janabk{at}u.washington.edu.
Little is known about the behavior of hematopoietic stem cells (HSC) in primates, as direct observations and competitive repopulation assays are not feasible. Therefore, we used two different and independent experimental strategies: the tracking of transgene expression after retroviral-mediated gene transfer (n=11 baboons; n=7 rhesus macaques) and quantitation of the average telomere length of granulocytes (n=132 baboons; n=14 macaques), together with stochastic methods, to study HSC kinetics in vivo. The average replication rate for baboon HSC is once per 36 weeks using gene marking analyses and once per 23 weeks using telomere shortening analyses. Comparable results were derived from the macaque data. These rates are substantially slower than the average replication rates previously reported for HSC in mice (once per 2.5 weeks) and cats (once per 8.3 weeks). Since baboons and macaques live for 25-45 years, much longer than mice (approximately 2 years) and cats (12-18 years), we can compute that HSC undergo a relatively constant number (~80-200) of lifetime replications. Our data thus suggest that the self-renewal capacity of mammalian stem cells in vivo is defined and evolutionarily conserved.

CiteULike Connotea Del.icio.us Digg Reddit Technorati What's this?
This article has been cited by other articles:

|
 |

|
 |
 
A. W. Nienhuis
Development of gene therapy for blood disorders
Blood,
May 1, 2008;
111(9):
4431 - 4444.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|
|