Identification of podocalyxin-like protein 1 as a novel cell surface marker for hemangioblasts in the murine aorta-gonad-mesonephros region

被引:90
作者
Hara, T
Nakano, Y
Tanaka, M
Tamura, K
Sekiguchi, T
Minehata, K
Copeland, NG
Jenkins, NA
Okabe, M
Kogo, H
Mukouyama, Y
Miyajima, A
机构
[1] Univ Tokyo, Inst Mol & Cellular Biosci, Bunkyo Ku, Tokyo 1130032, Japan
[2] Univ Tokyo, Core Res Evolut Sci & Technol, Bunkyo Ku, Tokyo 1130032, Japan
[3] Tokyo Univ Pharm & Life Sci, Hachioji, Tokyo 1920355, Japan
[4] NCI, Mammalian Genet Lab, ABL Basic Res Program, Frederick Canc Res & Dev Ctr, Frederick, MD 21702 USA
[5] Osaka Univ, Genome Informat Res Ctr, Suita, Osaka 5650871, Japan
关键词
D O I
10.1016/S1074-7613(00)80132-6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recent studies with avian embryos and murine embryonic stem cells have suggested that hematopoietic cells are derived from hemangioblasts, the common precursors of hematopoietic and endothelial cells. We molecularly cloned podocalyxin-like protein 1 (PCLP1) as a novel surface marker for endothelial-like cells in the aorta-gonad-mesonephros (AGM) region of mouse embryos, where long-term repopulating hematopoietic stem cells (LTR-HSCs) are known to arise. PCLP1(+) CD45(-) cells in the AGM region incorporated acetylated low-density lipoprotein and produced both hematopoietic and endothelial cells when cocultured with OP9 stromal cells. Moreover, multiple lineages of hematopoietic cells were generated in vivo when PCLP1(+)CD45(-) cells were injected into neonatal liver of busulfan-treated mice. Thus, PCLP1 can be used to separate hemangioblasts that give rise to LTR-HSCs.
引用
收藏
页码:567 / 578
页数:12
相关论文
共 49 条
  • [1] Choi K, 1998, DEVELOPMENT, V125, P725
  • [2] DEVELOPMENT AND APPLICATIONS OF A MOLECULAR GENETIC-LINKAGE MAP OF THE MOUSE GENOME
    COPELAND, NG
    JENKINS, NA
    [J]. TRENDS IN GENETICS, 1991, 7 (04) : 113 - 118
  • [3] Circulation of hematopoietic progenitors in the mouse embryo
    Delassus, S
    Cumano, A
    [J]. IMMUNITY, 1996, 4 (01) : 97 - 106
  • [4] DICKSON MC, 1995, DEVELOPMENT, V121, P1845
  • [5] Qualitative and quantitative aspects of haematopoietic cell development in the mammalian embryo
    Dzierzak, E
    Medvinsky, A
    de Bruijn, M
    [J]. IMMUNOLOGY TODAY, 1998, 19 (05): : 228 - 236
  • [6] Ligand-dependent development of the endothelial and hemopoietic lineages from embryonic mesodermal cells expressing vascular endothelial growth factor receptor 2
    Eichmann, A
    Corbel, C
    Nataf, V
    Vaigot, P
    Breant, C
    LeDouarin, NM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (10) : 5141 - 5146
  • [7] The SCL gene specifies haemangioblast development from early mesoderm
    Gering, M
    Rodaway, ARF
    Göttgens, B
    Patient, RK
    Green, AR
    [J]. EMBO JOURNAL, 1998, 17 (14) : 4029 - 4045
  • [8] EMERGENCE OF MULTIPOTENT HEMATOPOIETIC-CELLS IN THE YOLK-SAC AND PARAAORTIC SPLANCHNOPLEURA IN MOUSE EMBRYOS, BEGINNING AT 8.5 DAYS POSTCOITUS
    GODIN, I
    DIETERLENLIEVRE, F
    CUMANO, A
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (03) : 773 - 777
  • [9] Distinct roles of oncostatin M and leukemia inhibitory factor in the development of primordial germ cells and Sertoli cells in mice
    Hara, T
    Tamura, K
    de Miguel, MP
    Mukouyama, Y
    Kim, HJ
    Kogo, H
    Donovan, PJ
    Miyajima, A
    [J]. DEVELOPMENTAL BIOLOGY, 1998, 201 (02) : 144 - 153
  • [10] EXPRESSION CLONING OF A CDNA-ENCODING THE MURINE INTERLEUKIN-4 RECEPTOR BASED ON LIGAND-BINDING
    HARADA, N
    CASTLE, BE
    GORMAN, DM
    ITOH, N
    SCHREURS, J
    BARRETT, RL
    HOWARD, M
    MIYAJIMA, A
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (03) : 857 - 861