A non-transmembrane form of jagged-1 regulates the formation of matrix-dependent chord-like structures

被引:26
作者
Wong, MKK
Prudovsky, I
Vary, C
Booth, C
Liaw, L
Mousa, S
Small, D
Maciag, T
机构
[1] Univ Pittsburgh, Inst Canc, Div Hematol Oncol, Pittsburgh, PA 15213 USA
[2] Dupont Pharmaceut, Cardiovasc Biol Grp, Wilmington, DE 19880 USA
[3] Maine Med Ctr, Res Inst, Ctr Mol Med, S Portland, ME 04106 USA
关键词
D O I
10.1006/bbrc.2000.2173
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
Jagged-Notch interactions regulate a transmembrane ligand-receptor signaling pathway involved in the regulation of cell. fate determination as well as myoblast and endothelial cell differentiation. To further examine the role of the transmembrane ligand, Jagged-1, in the regulation of cell differentiation, we stably transfected NIH 3T3 cells with a truncated form of Jagged(J)-1, which results in the secretion of a soluble(s) form of the protein. Comparison of gene expression by serial analysis demonstrated that among the 227 transcripts differentially regulated in the sJ-1 transfectants, the expression of the pro-alpha-2(I) collagen transcript and pro-alpha-1(I) collagen translation product was predominantly repressed in sJ-1 transfectants. When plated on extracellular matrices, sJ-1 transfectants formed prominent chord-like structures on type I collagen but not on fibrin, fibronectin, or vitronectin. While the sJ-1 transfectants exhibited growth kinetics similar to control cells and were unable to grow in soft agar, the cells were less sensitive to contact inhibition of growth in vitro and sJ-1 allografts formed tissue masses in nude mice after a prolonged latency period and exhibited an abundance of host-derived microvascular endothelial cells. These data suggest that J-1 may be able to modulate, in a matrix-dependent manner, the organization of cell to cell interactions including its ability to promote the development of chord-like structures. (C) 2000 Academic Press.
引用
收藏
页码:853 / 859
页数:7
相关论文
共 32 条
  • [1] [Anonymous], 1989, SYNTHETIC OLIGONUCLE
  • [2] SPACING DIFFERENTIATION IN THE DEVELOPING DROSOPHILA EYE - A FIBRINOGEN-RELATED LATERAL INHIBITOR ENCODED BY SCABROUS
    BAKER, NE
    MLODZIK, M
    RUBIN, GM
    [J]. SCIENCE, 1990, 250 (4986) : 1370 - 1377
  • [3] REQUIREMENT OF VASCULAR INTEGRIN ALPHA(V)BETA(3) FOR ANGIOGENESIS
    BROOKS, PC
    CLARK, RAF
    CHERESH, DA
    [J]. SCIENCE, 1994, 264 (5158) : 569 - 571
  • [4] Notch1-induced delay of human hematopoietic progenitor cell differentiation is associated with altered cell cycle kinetics
    Carlesso, N
    Aster, JC
    Sklar, J
    Scadden, DT
    [J]. BLOOD, 1999, 93 (03) : 838 - 848
  • [5] EVIDENCE OF THE PRESENCE OF A SPECIFIC VASCULAR ENDOTHELIAL GROWTH-FACTOR IN FETAL BOVINE RETINA
    CHEN, CH
    CHEN, SC
    [J]. EXPERIMENTAL CELL RESEARCH, 1987, 169 (02) : 287 - 295
  • [6] COLLINS T, 1993, LAB INVEST, V68, P499
  • [7] Blood vessel formation: What is its molecular basis?
    Folkman, J
    DAmore, PA
    [J]. CELL, 1996, 87 (07) : 1153 - 1155
  • [8] FOROUGH R, 1993, J BIOL CHEM, V268, P2960
  • [9] INHIBITION OF ENDOTHELIAL-CELL PROLIFERATION BY GAMMA-INTERFERON
    FRIESEL, R
    KOMORIYA, A
    MACIAG, T
    [J]. JOURNAL OF CELL BIOLOGY, 1987, 104 (03) : 689 - 696
  • [10] ISOLATION OF IMMEDIATE-EARLY DIFFERENTIATION MESSENGER-RNAS BY ENZYMATIC AMPLIFICATION OF SUBTRACTED CDNA FROM HUMAN ENDOTHELIAL-CELLS
    HLA, T
    MACIAG, T
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 167 (02) : 637 - 643