The ABC transporter Bcrp1/ABCG2 is expressed in a wide variety of stem cells and is a molecular determinant of the side-population phenotype

被引:1707
作者
Zhou, S
Schuetz, JD
Bunting, KD
Colapietro, AM
Sampath, J
Morris, JJ
Lagutina, I
Grosveld, GC
Osawa, M
Nakauchi, H
Sorrentino, BP
机构
[1] St Jude Childrens Res Hosp, Dept Hematol Oncol, Div Expt Hematol, Memphis, TN 38105 USA
[2] St Jude Childrens Res Hosp, Dept Pharmaceut Sci, Memphis, TN 38105 USA
[3] St Jude Childrens Res Hosp, Dept Genet, Memphis, TN 38105 USA
[4] Univ Tsukuba, Inst Basic Med Sci, Dept Immunol, Tsukuba, Ibaraki, Japan
关键词
D O I
10.1038/nm0901-1028
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Stem cells from bone marrow, skeletal muscle and possibly other tissues can be identified by the 'side-population' (SP) phenotype. Although it has been assumed that expression of ABC transporters is responsible for this phenotype, the specific molecules involved have not been defined. Here we show that expression of the Bcrp1 (also known as Abcg2 murine/ABCG2 human) gene is a conserved feature of stem cells from a wide variety of sources. Bcrp1 mRNA was expressed at high levels in primitive murine hematopoietic stem cells, and was sharply downregulated with differentiation. Enforced expression of the ABCG2 cDNA directly conferred the SP phenotype to bone-marrow cells and caused a reduction in maturing progeny both in vitro and in transplantation-based assays. These results show that expression of the Bcrp1/ABCG2 gene is an important determinant of the SP phenotype, and that it might serve as a marker for stem cells from various sources.
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收藏
页码:1028 / 1034
页数:7
相关论文
共 38 条
  • [1] Sensitization of hematopoietic stem and progenitor cells to trimetrexate using nucleoside transport inhibitors
    Allay, JA
    Spencer, HT
    Wilkinson, SL
    Belt, JA
    Blakley, RL
    Sorrentino, BP
    [J]. BLOOD, 1997, 90 (09) : 3546 - 3554
  • [2] In vivo selection of retrovirally transduced hematopoietic stem cells
    Allay, JA
    Persons, DA
    Galipeau, J
    Riberdy, JM
    Ashmun, RA
    Blakley, RL
    Sorrentino, BP
    [J]. NATURE MEDICINE, 1998, 4 (10) : 1136 - 1143
  • [3] Bodine DM, 1996, BLOOD, V88, P89
  • [4] Enforced P-glycoprotein pump function in murine bone marrow cells results in expansion of side population stem cells in vitro and repopulating cells in vivo
    Bunting, KD
    Zhou, S
    Lu, TH
    Sorrentino, BP
    [J]. BLOOD, 2000, 96 (03) : 902 - 909
  • [5] Transduction of murine bone marrow cells with an MDR1 vector enables ex vivo stem cell expansion, but these expanded grafts cause a myeloproliferative syndrome in transplanted mice
    Bunting, KD
    Galipeau, J
    Topham, D
    Benaim, E
    Sorrentino, BP
    [J]. BLOOD, 1998, 92 (07) : 2269 - 2279
  • [6] EXPRESSION AND ACTIVITY OF P-GLYCOPROTEIN, A MULTIDRUG EFFLUX PUMP, IN HUMAN HEMATOPOIETIC STEM-CELLS
    CHAUDHARY, PM
    RONINSON, IB
    [J]. CELL, 1991, 66 (01) : 85 - 94
  • [7] Retrovirus-mediated gene transfer of the multidrug resistance-associated protein (MRP) cDNA protects cells from chemotherapeutic agents
    DHondt, V
    Caruso, M
    Bank, A
    [J]. HUMAN GENE THERAPY, 1997, 8 (15) : 1745 - 1751
  • [8] Doyle LA, 1999, P NATL ACAD SCI USA, V96, P2569
  • [9] A multidrug resistance transporter from human MCF-7 breast cancer cells
    Doyle, LA
    Yang, WD
    Abruzzo, LV
    Krogmann, T
    Gao, YM
    Rishi, AK
    Ross, DD
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (26) : 15665 - 15670
  • [10] A genetic analysis of neural progenitor differentiation
    Geschwind, DH
    Ou, J
    Easterday, MC
    Dougherty, JD
    Jackson, RL
    Chen, ZG
    Antoine, H
    Terskikh, A
    Weissman, IL
    Nelson, SF
    Kornblum, HI
    [J]. NEURON, 2001, 29 (02) : 325 - 339