Notch-1 and Notch-2 exhibit unique patterns of expression in human B-lineage cells

被引:41
作者
Bertrand, FE
Eckfeldt, CE
Lysholm, AS
LeBien, TW
机构
[1] Univ Minnesota, Ctr Canc, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Lab Med & Pathol, Minneapolis, MN 55455 USA
关键词
Notch; B cell precursors;
D O I
10.1038/sj.leu.2401942
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The Notch genes encode a conserved family of receptors that influence developmental fate in many species. Prior studies have indicated that Notch-1 and Notch-2 signaling influence the development of hematopoietic stems cells and thymocytes, but little is known regarding Notch expression and function in B-lineage cells. We analyzed the expression of Notch receptors and Notch ligands in human B-lineage cells and bone marrow (BM) stromal cells. Notch-1 mRNA and protein is expressed throughout normal B cell development and in leukemic B-lineage cells. In contrast, Notch-2 expression is limited to pre B cells expressing low levels of surface mu. The Notch ligand Delta is expressed in BM B-lineage cells. The Notch ligand Jagged-1 is not expressed in B-lineage cells, but is expressed in BM stromal cells. These results suggest a model wherein lateral signaling between Notch and Delta on B-lineage cells and/or Notch/Jagged-1 interactions between B-lineage cells and BM stromal cells may regulate human B cell development.
引用
收藏
页码:2095 / 2102
页数:8
相关论文
共 51 条
[1]   Notch signaling: Cell fate control and signal integration in development [J].
Artavanis-Tsakonas, S ;
Rand, MD ;
Lake, RJ .
SCIENCE, 1999, 284 (5415) :770-776
[2]   FUNCTIONAL-ANALYSIS OF THE TAN-1 GENE, A HUMAN HOMOLOG OF DROSOPHILA NOTCH [J].
ASTER, J ;
PEAR, W ;
HASSERJIAN, R ;
ERBA, H ;
DAVI, F ;
LUO, B ;
SCOTT, M ;
BALTIMORE, D ;
SKLAR, J .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1994, 59 :125-136
[3]   Rel/NF-κB can trigger the Notch signaling pathway by inducing the expression of Jagged1, a ligand for Notch receptors [J].
Bash, J ;
Zong, WX ;
Banga, S ;
Rivera, A ;
Ballard, DW ;
Ron, Y ;
Gélinas, C .
EMBO JOURNAL, 1999, 18 (10) :2803-2811
[4]   Lack of requirement for Presenilin1 in Notch1 signaling [J].
Berechid, BE ;
Thinakaran, G ;
Wong, PC ;
Sisodia, SS ;
Nye, JS .
CURRENT BIOLOGY, 1999, 9 (24) :1493-1496
[5]   Ig D-H gene segment transcription and rearrangement before surface expression of the pan-B cell marker CD19 in normal human bone marrow [J].
Bertrand, FE ;
Billips, LG ;
Burrows, PD ;
Gartland, GL ;
Kubagawa, H ;
Schroeder, HW .
BLOOD, 1997, 90 (02) :736-744
[6]   Notch1 and Notch2 inhibit myeloid differentiation in response to different cytokines [J].
Bigas, A ;
Martin, DIK ;
Milner, LA .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (04) :2324-2333
[7]   A novel proteolytic cleavage involved in Notch signaling:: The role of the disintegrin-metalloprotease TACE [J].
Brou, C ;
Logeat, F ;
Gupta, N ;
Bessia, C ;
LeBail, O ;
Doedens, JR ;
Cumano, A ;
Roux, P ;
Black, RA ;
Israël, A .
MOLECULAR CELL, 2000, 5 (02) :207-216
[8]   B cell development and differentiation [J].
Burrows, PD ;
Cooper, MD .
CURRENT OPINION IN IMMUNOLOGY, 1997, 9 (02) :239-244
[9]   Intracellular forms of human NOTCH1 interact at distinctly different levels with RBP-Jkappa in human B and T cells [J].
Callahan, J ;
Aster, J ;
Sklar, J ;
Kieff, E ;
Robertson, ES .
LEUKEMIA, 2000, 14 (01) :84-92
[10]   Notch1-induced delay of human hematopoietic progenitor cell differentiation is associated with altered cell cycle kinetics [J].
Carlesso, N ;
Aster, JC ;
Sklar, J ;
Scadden, DT .
BLOOD, 1999, 93 (03) :838-848