Stromal expression of Jagged 1 promotes colony formation by fetal hematopoietic progenitor cells

被引:135
作者
Jones, P
May, G
Healy, L
Brown, J
Hoyne, G
Delassus, S
Enver, T
机构
[1] Inst Canc Res, Chester Beatty Labs, Sect Gene Funct & Regulat, London SW3 6JB, England
[2] Inst Canc Res, Chester Beatty Labs, Leukaemia Res Fund Ctr, London SW3 6JB, England
[3] Univ Edinburgh, Dept Resp Med, Edinburgh, Midlothian, Scotland
关键词
D O I
10.1182/blood.V92.5.1505.417k42_1505_1511
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The Notch signaling system regulates proliferation and differentiation in many tissues. Notch is a transmembrane receptor activated by ligands expressed on adjacent cells. Hematopoietic stem cells and early progenitors express Notch, making the stromal cells which form cell-cell contacts with progenitor cells candidate ligand-presenting cells in the hematopoietic microenvironment. Therefore, we examined primary stromal eel cultures for expression of Notch ligands. Using reverse transcription-polymerase chain reaction, in situ hybridization, immunohistochemistry, and Western blotting, we demonstrate expression of Jagged 1 in primary stromal cultures. To investigate if the stromal expression of Jagged 1 has functional effects on hematopoietic progenitors, we cultured CD34(+), c-kit(+) hematopoietic progenitor cells derived from the aorto gonadal mesonephros region of day 11 mouse embryos on the Jagged 1(-) stromal cell line S17 and on S17 cells engineered to express Jagged 1. The presence of Jagged 1 increased the number of colonies formed in subsequent methylcellulose culture fourfold. Larger increases in colony numbers were observed under the same culture conditions with CD34(+), c-kit(+) hematopoietic progenitor cells derived from d11 fetal liver. These results obtained in vitro table Jagged 1 as a candidate regulator of stem cell fate in the context of stromal microenvironments in vivo. (C) 1998 by The American Society of Hematology.
引用
收藏
页码:1505 / 1511
页数:7
相关论文
共 37 条
  • [1] ALLEN TD, 1997, HEMATOPOIETIC LINEAG, P29
  • [2] BENTLEY SA, 1981, EXP HEMATOL, V9, P303
  • [3] BETTENHAUSEN B, 1995, DEVELOPMENT, V121, P2407
  • [4] Notch1 and Notch2 inhibit myeloid differentiation in response to different cytokines
    Bigas, A
    Martin, DIK
    Milner, LA
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (04) : 2324 - 2333
  • [5] DECIMO D, 1995, GENE PROBES, V2, P169
  • [6] Dunwoodie SL, 1997, DEVELOPMENT, V124, P3065
  • [7] TAN-1, THE HUMAN HOMOLOG OF THE DROSOPHILA NOTCH GENE, IS BROKEN BY CHROMOSOMAL TRANSLOCATIONS IN T-LYMPHOBLASTIC NEOPLASMS
    ELLISEN, LW
    BIRD, J
    WEST, DC
    SORENG, AL
    REYNOLDS, TC
    SMITH, SD
    SKLAR, J
    [J]. CELL, 1991, 66 (04) : 649 - 661
  • [8] AN ACTIVATED NOTCH RECEPTOR BLOCKS CELL-FATE COMMITMENT IN THE DEVELOPING DROSOPHILA EYE
    FORTINI, ME
    REBAY, I
    CARON, LA
    ARTAVANISTSAKONAS, S
    [J]. NATURE, 1993, 365 (6446) : 555 - 557
  • [9] Frequent provirus insertional mutagenesis of Notch1 in thymomas of MMTV(D)/myc transgenic mice suggests a collaboration of c-myc and Notch1 for oncogenesis
    Girard, L
    Hanna, Z
    Beaulieu, N
    Hoemann, CD
    Simard, C
    Kozak, CA
    Jolicoeur, P
    [J]. GENES & DEVELOPMENT, 1996, 10 (15) : 1930 - 1944
  • [10] 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