The Endoglinpositive Sca-1Positive Rhodaminelow phenotype defines a near-homogeneous population of long-term repopulating hematopoietic stem cells

被引:63
作者
Chen, CZ
Li, L
Li, M
Lodish, HF
机构
[1] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[2] MIT, Dept Biol, Cambridge, MA 02142 USA
关键词
D O I
10.1016/S1074-7613(03)00265-6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Endoglin, an ancillary TGF-beta receptor, is differentially expressed in long-term repopulating hematopoietic stem cells (LTR-HSC). Here, we describe simple and highly efficient purification schemes for mouse bone marrow LTR-HSCs using Endoglin as a marker. The Endoglin positive and Sca-1 positive (Endo(Pos) Sca-1(Pos)) population, which contains about 36% of "Side Population" (SP) cells, is highly enriched for LTR-HSCs. In long-term competitive reconstitution assays, 100 such cells reconstituted all lethally irradiated recipients. Interestingly, the Endo(Pos) Sca-1(Pos) population contains comparable LTR-HSC activity in both SP and non-SP fractions, indicating that many HSCs are not captured by the SP phenotype. Furthermore, LTR-HSCs are exclusively found in the End(Pos) Sca-1(Pos) Lin(Neg/Low) (lineage negative/low), but not in the Endo(Neg) Sca-1(Pos) Lin(Neg/Low) population, suggesting that the Endo(Pos) population may contain all LTR-HSCs in mouse bone marrow. Finally, we demonstrated that the Endo(Pos) Sca-1(Pos) Rh-Low (Rhodamine-123 low) phenotype, without using CD34, c-Kit, or Lineage markers, defines a nearly homogenous population of LTR-HSCs.
引用
收藏
页码:525 / 533
页数:9
相关论文
共 22 条
[1]   IDENTIFICATION IN ADULT BONE-MARROW OF PLURIPOTENT AND RESTRICTED STEM-CELLS OF MYELOID AND LYMPHOID SYSTEMS [J].
ABRAMSON, S ;
MILLER, RG ;
PHILLIPS, RA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1977, 145 (06) :1567-1579
[2]   Endoglin, an ancillary TGFβ receptor, is required for extraembryonic angiogenesis and plays a key role in heart development [J].
Arthur, HM ;
Ure, J ;
Smith, AJH ;
Renforth, G ;
Wilson, DI ;
Torsney, E ;
Charlton, R ;
Parums, DV ;
Jowett, T ;
Marchuk, DA ;
Burn, J ;
Diamond, AG .
DEVELOPMENTAL BIOLOGY, 2000, 217 (01) :42-53
[3]  
Azuma Hiroyuki, 2000, Journal of Medical Investigation, V47, P81
[4]   Identification of endoglin as a functional marker that defines long-term repopulating hematopoietic stem cells [J].
Chen, CZ ;
Li, M ;
de Graaf, D ;
Monti, S ;
Göttgens, B ;
Sanchez, MJ ;
Lander, ES ;
Golub, TR ;
Green, AR ;
Lodish, HF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (24) :15468-15473
[5]   Isolation and functional properties of murine hematopoietic stem cells that are replicating in vivo [J].
Goodell, MA ;
Brose, K ;
Paradis, G ;
Conner, AS ;
Mulligan, RC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (04) :1797-1806
[6]  
HARRISON DE, 1993, EXP HEMATOL, V21, P206
[7]   A stem cell molecular signature [J].
Ivanova, NB ;
Dimos, JT ;
Schaniel, C ;
Hackney, JA ;
Moore, KA ;
Lemischka, IR .
SCIENCE, 2002, 298 (5593) :601-604
[8]   CLONAL AND SYSTEMIC ANALYSIS OF LONG-TERM HEMATOPOIESIS IN THE MOUSE [J].
JORDAN, CT ;
LEMISCHKA, IR .
GENES & DEVELOPMENT, 1990, 4 (02) :220-232
[9]   CELLULAR AND DEVELOPMENTAL PROPERTIES OF FETAL HEMATOPOIETIC STEM-CELLS [J].
JORDAN, CT ;
MCKEARN, JP ;
LEMISCHKA, IR .
CELL, 1990, 61 (06) :953-963
[10]   Functional characterization of a novel hematopoietic stem cell and its place in the c-kit maturation pathway in bone marrow cell development [J].
Ortiz, M ;
Wine, JW ;
Lohrey, N ;
Ruscetti, FW ;
Spence, SE ;
Keller, JR .
IMMUNITY, 1999, 10 (02) :173-182