Hematopoietic stem-cell behavior in nonhuman primates

被引:63
作者
Shepherd, Bryan E.
Kiem, Hans-Peter
Lansdorp, Peter M.
Dunbar, Cynthia E.
Aubert, Geraldine
LaRochelle, Andre
Seggewiss, Ruth
Guttorp, Peter
Abkowitz, Janis L.
机构
[1] Vanderbilt Univ, Dept Biostat, Nashville, TN USA
[2] Fred Hutchinson Canc Res Inst, Seattle, WA USA
[3] Univ British Columbia, Terry Fox Lab, British Columbia Canc Agcy, Vancouver, BC V5Z 1M9, Canada
[4] Univ British Columbia, Dept Med, Vancouver, BC V5Z 1M9, Canada
[5] NHLBI, NIH, Bethesda, MD 20892 USA
[6] Univ Washington, Dept Stat, Seattle, WA 98195 USA
[7] Univ Washington, Dept Med Hematol, Seattle, WA 98195 USA
关键词
D O I
10.1182/blood-2007-02-075382
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Little is known about the behavior of hematopoietic stem cells (HSCs) in primates because direct observations and competitive-repopulation assays are not feasible. Therefore, we used 2 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 HSCs is once per 36 weeks according to gene-marking analyses and once per 23 weeks according to telomere-shortening analyses. Comparable results were derived from the macaque data. These rates are substantially slower than the average replication rates previously reported for HSCs in mice (once per 2.5 weeks) and cats (once per 8.3 weeks). Because baboons and macaques live for 25 to 45 years, much longer than mice (similar to 2 years) and cats (12-18 years), we can compute that HSCs undergo a relatively constant number (similar to 80-200) of lifetime replications. Thus, our data suggest that the self-renewal capacity of mammalian stem cells in vivo is defined and evolutionarily conserved.
引用
收藏
页码:1806 / 1813
页数:8
相关论文
共 51 条
[1]   In vivo kinetics of murine hemopoietic stem cells [J].
Abkowitz, JL ;
Golinelli, D ;
Harrison, DE ;
Guttorp, P .
BLOOD, 2000, 96 (10) :3399-3405
[2]   Evidence that the number of hematopoietic stem cells per animal is conserved in mammals [J].
Abkowitz, JL ;
Catlin, SN ;
McCallie, MT ;
Guttorp, P .
BLOOD, 2002, 100 (07) :2665-2667
[3]   BEHAVIOR OF HEMATOPOIETIC STEM-CELLS IN A LARGE ANIMAL [J].
ABKOWITZ, JL ;
PERSIK, MT ;
SHELTON, GH ;
OTT, RL ;
KIKLEVICH, JV ;
CATLIN, SN ;
GUTTORP, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (06) :2031-2035
[4]   Evidence that hematopoiesis may be a stochastic process in vivo [J].
Abkowitz, JL ;
Catlin, SN ;
Guttorp, P .
NATURE MEDICINE, 1996, 2 (02) :190-197
[5]   Longitudinal data on telomere length in leukocytes from newborn baboons support a marked drop in stem cell turnover around 1 year of age [J].
Baerlocher, Gabriela M. ;
Rice, Karen ;
Vulto, Irma ;
Lansdorp, Peter M. .
AGING CELL, 2007, 6 (01) :121-123
[6]   Telomere shortening in leukocyte subpopulations from baboons [J].
Baerlocher, GM ;
Mak, J ;
Röth, A ;
Rice, KS ;
Lansdorp, PM .
JOURNAL OF LEUKOCYTE BIOLOGY, 2003, 73 (02) :289-296
[7]   Telomere length measurement by fluorescence in situ hybridization and flow cytometry: Tips and pitfalls [J].
Baerlocher, GM ;
Mak, J ;
Tien, T ;
Lansdorp, PM .
CYTOMETRY, 2002, 47 (02) :89-99
[8]   Efficient transduction and engraftment of G-CSF-mobilized peripheral blood CD34+ cells in nonhuman primates using GALV-pseudotyped gammaretroviral vectors [J].
Beard, Brian C. ;
Mezquita, Pau ;
Morris, Julia C. ;
Kiem, Hans-Peter .
MOLECULAR THERAPY, 2006, 14 (02) :212-217
[9]   Hematopoietic stem cells engraft in mice with absolute efficiency [J].
Benveniste, P ;
Cantin, C ;
Hyam, D ;
Iscove, NN .
NATURE IMMUNOLOGY, 2003, 4 (07) :708-713
[10]  
Bradford GB, 1997, EXP HEMATOL, V25, P445