Suppression of apoptosis by inhibition of phosphatidylcholine-specific phospholipase C in vascular endothelial cells

被引:24
作者
Miao, JY
Kaji, K
Hayashi, H
Araki, S [1 ]
机构
[1] Nagoya Univ, Sch Sci, Sugashima Marine Biol Lab, Toba, Mie 517, Japan
[2] Tokyo Metropolitan Inst Gerontol, Itabashi Ku, Tokyo 173, Japan
来源
ENDOTHELIUM-NEW YORK | 1997年 / 5卷 / 04期
关键词
apoptosis; endothelial cells; PC-PLC; signal transduction;
D O I
10.3109/10623329709052588
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In order to clarify the role of phosphatidylcholine-specific phospholipase C (PC-PLC) in the regulation of apoptosis in vascular endothelial cells (VEC), we investigated the effects of D609, a specific inhibitor of PC-PLC, on apoptosis that was induced by deprivation of fibroblast growth factor (FGF) and serum and also by rattlesnake venom. The early morphological changes (detachment of cells from dishes) and the fragmentation of DNA, which is a specific feature of apoptotic cell death, were clearly inhibited by D609 in these two apoptosis-inducing systems. Moreover, the production of diacylglycerol (DAG), which was stimulated in apoptotic VEC, was suppressed by D609. The effects of D609 on the activity of PC-PLC and on apoptosis of VEC were dose-dependent. Our results indicate that PC-PLC is involved in the apoptosis-inducing signal pathway in VEC and, that DAG, produced from phosphatidylcholine (PC), might be an important mediator in this signal-transduction pathway. Our results also suggest that rattlesnake venom, a strong promoter of apoptosis in VEC, might induce apoptosis bg stimulating PC-PLC and, furthermore, that PC-PLC might play a significant role in anchorage-dependent signal transduction in VEC.
引用
收藏
页码:231 / 239
页数:9
相关论文
共 24 条
  • [1] INDUCTION OF APOPTOSIS BY HEMORRHAGIC SNAKE-VENOM IN VASCULAR ENDOTHELIAL-CELLS
    ARAKI, S
    ISHIDA, T
    YAMAMOTO, T
    KAJI, K
    HAYASHI, H
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 190 (01) : 148 - 153
  • [2] APOPTOSIS OF VASCULAR ENDOTHELIAL-CELLS BY FIBROBLAST GROWTH-FACTOR DEPRIVATION
    ARAKI, S
    SHIMADA, Y
    KAJI, K
    HAYASHI, H
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 168 (03) : 1194 - 1200
  • [3] PROGRAMMED CELL-DEATH IN RESPONSE TO ALKYLLYSOPHOSPHOLIPIDS IN ENDOTHELIAL-CELLS
    ARAKI, S
    TSUNA, I
    KAJI, K
    HAYASHI, H
    [J]. JOURNAL OF BIOCHEMISTRY, 1994, 115 (02) : 245 - 247
  • [4] BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
  • [5] MULTIPLE PATHWAYS ORIGINATE AT THE FAS/APO-1 (CD95) RECEPTOR - SEQUENTIAL INVOLVEMENT OF PHOSPHATIDYLCHOLINE-SPECIFIC PHOSPHOLIPASE-C AND ACIDIC SPHINGOMYELINASE IN THE PROPAGATION OF THE APOPTOTIC SIGNAL
    CIFONE, MG
    RONCAIOLI, P
    DEMARIA, R
    CAMARDA, G
    SANTONI, A
    RUBERTI, G
    TESTI, R
    [J]. EMBO JOURNAL, 1995, 14 (23) : 5859 - 5868
  • [6] PHOSPHOLIPID SIGNALING
    DIVECHA, N
    IRVINE, RF
    [J]. CELL, 1995, 80 (02) : 269 - 278
  • [7] ROLE OF CELL-SHAPE IN GROWTH-CONTROL
    FOLKMAN, J
    MOSCONA, A
    [J]. NATURE, 1978, 273 (5661) : 345 - 349
  • [8] EVIDENCE FOR INVOLVEMENT OF PHOSPHATIDYLCHOLINE-PHOSPHOLIPASE-C AND PROTEIN-KINASE-C IN TRANSFORMING GROWTH-FACTOR-BETA SIGNALING
    HALSTEAD, J
    KEMP, A
    IGNOTZ, RA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (23) : 13600 - 13603
  • [9] CLASSIFICATION OF SIGNALS FOR BLOCKING APOPTOSIS IN VASCULAR ENDOTHELIAL-CELLS
    HASE, M
    ARAKI, S
    KAJI, K
    HAYASHI, H
    [J]. JOURNAL OF BIOCHEMISTRY, 1994, 116 (04) : 905 - 909
  • [10] Drosophila homologs of baculovirus inhibitor of apoptosis proteins function to block cell death
    Hay, BA
    Wassarman, DA
    Rubin, GM
    [J]. CELL, 1995, 83 (07) : 1253 - 1262