Cytokine receptor repertoire and cytokine responsiveness of Hodull/Rhdull dull stem cells with differing potentials for G1/S phase progression

被引:30
作者
Reddy, GPV
McAuliffe, CM
Pang, LZ
Quesenberry, PJ
Bertoncello, I
机构
[1] Peter MacCallum Canc Inst, Trescowthick Res Labs, Melbourne, Vic 8006, Australia
[2] Henry Ford Hlth Sci Ctr, Vattikuti Urol Inst, Detroit, MI USA
[3] Univ Massachusetts, Ctr Canc, Worcester, MA 01605 USA
[4] Roger Williams Hosp, Providence, RI USA
关键词
D O I
10.1016/S0301-472X(02)00814-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. Subsetting of Hoechst 33342 dull (Ho-dull) hematopoietic stem cells on the basis of rhodamine 123 (Rh) efflux utilizing an improved dual-dye efflux strategy resolves Ho-dull/Rh-dull stem cell subsets that differ with regard to their rate of recruitment and progression through the cell cycle upon exposure to cytokines. Materials and Methods. Murine bone marrow cells were isolated by negative immunomagnetic selection using lineage-directed antibodies followed by Ho and Rh staining using a dual-dye efflux method. Results. Ho-dull/Rh-dull stem cells that efflux Rh more efficiently (R1) exhibit a 4- to 8-hour delay in progression to S phase when stimulated by interleukin-3 (IL-3), IL-6, IL-11, and stem cell factor (SCF) compared to Ho-dull/Rh-medium stem cells, which retain low levels of Rh (R2). R1 and R2 cells show a hierarchical entry into S phase upon exposure to any or all of these cytokines. The R1 subset contains proportionately more high proliferative potential colony-forming cells than the R2 subset, but equivalent levels of engraftable stem cells at 3 and 8 weeks after competitive transplantation. Both R1 and R2 cells express c-kit, IL-3R, and IL-11R, whereas IL-6R and c-fms are only expressed by RI or R2 cells, respectively. Cytokine stimulation of RI and R2 cells induced cell cycle progression with elevated or induced expression of c-kit, c-fins, IL-2R, and IL-6R. Conclusion. These studies indicate that primitive marrow stem cells can be further subsetted by degree of Rh staining to reveal important functional phenotypic differences between cells with different levels of Rh staining. (C) 2002 International Society for Experimental Hematology. Published by Elsevier Science Inc.
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页码:792 / 800
页数:9
相关论文
共 45 条
[1]  
BAINES P, 1983, EXP HEMATOL, V11, P701
[2]  
BARTELMEZ SH, 1989, EXP HEMATOL, V17, P240
[3]   Adhesion receptor expression by hematopoietic cell lines and murine progenitors: Modulation by cytokines and cell cycle status [J].
Becker, PS ;
Nilsson, SK ;
Li, ZF ;
Berrios, VM ;
Dooner, MS ;
Cooper, CL ;
Hsieh, CC ;
Quesenberry, PJ .
EXPERIMENTAL HEMATOLOGY, 1999, 27 (03) :533-541
[4]  
BERTONCELLO I, 1992, CURR TOP MICROBIOL, V177, P83
[5]  
BERTONCELLO I, 1985, EXP HEMATOL, V13, P999
[6]  
Bertoncello I, 1997, COLONY STIMULATING F, P35
[7]   Resolution of pluripotential intermediates in murine hematopoietic differentiation by global complementary DNA amplification from single cells: confirmation of assignments by expression profiling of cytokine receptor transcripts [J].
Billia, F ;
Barbara, M ;
McEwen, J ;
Trevisan, M ;
Iscove, NN .
BLOOD, 2001, 97 (08) :2257-2268
[8]  
BODINE DM, 1992, BLOOD, V79, P913
[9]  
Bradford GB, 1997, EXP HEMATOL, V25, P445
[10]   EFFECT OF OXYGEN-TENSION ON HEMATOPOIETIC AND FIBROBLAST CELL-PROLIFERATION INVITRO [J].
BRADLEY, TR ;
HODGSON, GS ;
ROSENDAAL, M .
JOURNAL OF CELLULAR PHYSIOLOGY, 1978, 97 (03) :517-522