The hematopoietic stem compartment consists of a limited number of discrete stem cell subsets

被引:164
作者
Sieburg, HB
Cho, RH
Dykstra, B
Uchida, N
Eaves, CJ
Muller-Sieburg, CE
机构
[1] Sidney Kimmel Canc Ctr, San Diego, CA 92112 USA
[2] British Columbia Canc Agcy, Terry Fox Lab, Vancouver, BC V5Z 1L3, Canada
[3] Univ British Columbia, Vancouver, BC V5Z 1M9, Canada
关键词
D O I
10.1182/blood-2005-07-2970
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hematopoietic stem cells (HSCs) display extensive heterogeneity in their behavior even when isolated as phenotypically homogeneous populations. It is not clear whether this heterogeneity reflects inherently diverse subsets of HSCs or a homogeneous population of HSCs diversified by their response to different external stimuli. To address this, we analyzed 97 individual HSCs in long-term transplantation assays. HSC clones were obtained from unseparated bone marrow (BM) through limiting dilution approaches. Following transplantation into individual hosts, donor-type cells in blood were measured bimonthly and the resulting repopulation kinetics were grouped according to overall shape. Only 16 types of repopulation kinetics were found among the HSC clones even though combinatorially 54 groups were possible. All HSC clones, regardless of their origin, could be assigned to this subset of groups, and the probability of finding new patterns is negligible. Thus, the full repertoire of repopulating HSCs was covered. These data indicate that the HSC compartment consists of a limited number of distinct HSC subsets, each with predictable behavior. Enrichment of HSCs (Lin-Rho-SP) changes the representation of HSC types by selecting for distinct subsets of HSCs. These data from the steady-state HSC repertoire could provide a basis for the diagnosis of perturbed patterns of HSCs potentially caused by disease or aging.
引用
收藏
页码:2311 / 2316
页数:6
相关论文
共 49 条
[41]   LONG-TERM REPOPULATION OF IRRADIATED MICE WITH LIMITING NUMBERS OF PURIFIED HEMATOPOIETIC STEM-CELLS - IN-VIVO EXPANSION OF STEM-CELL PHENOTYPE BUT NOT FUNCTION [J].
SPANGRUDE, GJ ;
BROOKS, DM ;
TUMAS, DB .
BLOOD, 1995, 85 (04) :1006-1016
[42]   RESTING AND ACTIVATED SUBSETS OF MOUSE MULTIPOTENT HEMATOPOIETIC STEM-CELLS [J].
SPANGRUDE, GJ ;
JOHNSON, GR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (19) :7433-7437
[43]   Early hematopoietic reconstitution after clinical stem cell transplantation: evidence for stochastic stem cell behavior and limited acceleration in telomere loss [J].
Thornley, I ;
Sutherland, R ;
Wynn, R ;
Nayar, R ;
Sung, L ;
Corpus, G ;
Kiss, T ;
Lipton, J ;
Doyle, J ;
Saunders, F ;
Kamel-Reid, S ;
Freedman, M ;
Messner, H .
BLOOD, 2002, 99 (07) :2387-2396
[44]   Enhanced in vivo regenerative potential of HOXB4-transduced hematopoietic stem cells with regulation of their pool size [J].
Thorsteinsdottir, U ;
Sauvageau, G ;
Humphries, RK .
BLOOD, 1999, 94 (08) :2605-2612
[45]   Cycle initiation and colony formation in culture by murine marrow cells with long-term reconstituting potential in vivo [J].
Trevisan, M ;
Yan, XQ ;
Iscove, NN .
BLOOD, 1996, 88 (11) :4149-4158
[46]   Different in vivo repopulating activities of purified hematopoietic stem cells before and after being stimulated to divide in vitro with the same kinetics [J].
Uchida, N ;
Dykstra, B ;
Lyons, KJ ;
Leung, FY ;
Eaves, CJ .
EXPERIMENTAL HEMATOLOGY, 2003, 31 (12) :1338-1347
[47]   GENETIC-CONTROL OF HEMATOPOIETIC KINETICS REVEALED BY ANALYSES OF ALLOPHENIC MICE AND STEM-CELL SUICIDE [J].
VANZANT, G ;
ELDRIDGE, PW ;
BEHRINGER, RR ;
DEWEY, MJ .
CELL, 1983, 35 (03) :639-645
[48]  
WINEMAN JP, 1992, BLOOD, V80, P1717
[49]  
Zhong RK, 1996, J IMMUNOL, V157, P138