A novel link between integrins, transmembrane-4 superfamily proteins (CD63 and CD81), and phosphatidylinositol 4-kinase

被引:224
作者
Berditchevski, F
Tolias, KF
Wong, K
Carpenter, CL
Hemler, ME
机构
[1] HARVARD UNIV,SCH MED,DANA FARBER CANC INST,BOSTON,MA 02115
[2] HARVARD UNIV,SCH MED,DIV SIGNAL TRANSDUCT,BETH ISRAEL HOSP,BOSTON,MA 02115
[3] HARVARD UNIV,SCH MED,DEPT CELL BIOL,BOSTON,MA 02115
[4] HARVARD UNIV,SCH MED,DEPT MED,BOSTON,MA 02115
关键词
D O I
10.1074/jbc.272.5.2595
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
Enzymatic and immunochemical assays show a phosphatidylinositol 4-kinase in novel and specific complexes with proteins (CD63 and CD81) of the transmembrane 4 superfamily (TM4SF) and an integrin (alpha(3) beta(1)). The size (55 kDa) and other properties of the phosphatidylinositol 4-kinase (PI 4-K) (stimulated by nonionic detergent, inhibited by adenosine, inhibited by monoclonal antibody 4CG5) are consistent with PI 4-K type II. Not only was PI 4-K associated with alpha(3) beta(1)-CD63 complexes in alpha(3)-transfected K562 cells, but also it could be co-purified from CD63 in untransfected K562 cells lacking alpha(3) beta(1). Thus, TM4SF proteins may link PI 4-K activity to the alpha(3) beta(1) integrin. The alpha(5) beta(1) integrin, which does not associate with TM4SF proteins, was not associated with PI 4-K. Notably, alpha(3) beta(1)-CD63-CD81-PI 4-K complexes are located in focal complexes at the cell periphery rather than in focal adhesions. The novel linkage between integrins, transmembrane 4 proteins, and phosphoinositide signaling at the cell periphery may play a key role in cell motility and provides a signaling pathway distinct hom conventional integrin signaling through focal adhesion kinase.
引用
收藏
页码:2595 / 2598
页数:4
相关论文
共 47 条
  • [21] COOPERATIVE SIGNALING BY ALPHA-5-BETA-1 AND ALPHA-4-BETA-1 INTEGRINS REGULATES METALLOPROTEINASE GENE-EXPRESSION IN FIBROBLASTS ADHERING TO FIBRONECTIN
    HUHTALA, P
    HUMPHRIES, MJ
    MCCARTHY, JB
    TREMBLE, PM
    WERB, Z
    DAMSKY, CH
    [J]. JOURNAL OF CELL BIOLOGY, 1995, 129 (03) : 867 - 879
  • [22] INTEGRINS - VERSATILITY, MODULATION, AND SIGNALING IN CELL-ADHESION
    HYNES, RO
    [J]. CELL, 1992, 69 (01) : 11 - 25
  • [23] IMAI T, 1993, J IMMUNOL, V151, P6470
  • [24] JULIANO RL, 1993, J CELL BIOL, V120, P557
  • [25] KORNBERG L, 1992, J BIOL CHEM, V267, P23439
  • [26] EXPRESSION OF INTEGRINS AND BASEMENT-MEMBRANE COMPONENTS BY WOUND KERATINOCYTES
    LARJAVA, H
    SALO, T
    HAAPASALMI, K
    KRAMER, RH
    HEINO, J
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (03) : 1425 - 1435
  • [27] INTEGRIN BETA-1-MEDIATED AND BETA-3-MEDIATED ENDOTHELIAL-CELL MIGRATION IS TRIGGERED THROUGH DISTINCT SIGNALING MECHANISMS
    LEAVESLEY, DI
    SCHWARTZ, MA
    ROSENFELD, M
    CHERESH, DA
    [J]. JOURNAL OF CELL BIOLOGY, 1993, 121 (01) : 163 - 170
  • [28] INTEGRIN-MEDIATED COLLAGEN MATRIX REORGANIZATION BY CULTURED HUMAN VASCULAR SMOOTH-MUSCLE CELLS
    LEE, RT
    BERDITCHEVSKI, F
    CHENG, GC
    HEMLER, ME
    [J]. CIRCULATION RESEARCH, 1995, 76 (02) : 209 - 214
  • [29] FOCAL ADHESION AS A SIGNAL-TRANSDUCTION ORGANELLE
    LO, SH
    CHEN, LB
    [J]. CANCER AND METASTASIS REVIEWS, 1994, 13 (01) : 9 - 24
  • [30] Mannion BA, 1996, J IMMUNOL, V157, P2039