Exposure to oxidized low-density lipoprotein reduces activable ras protein in vascular endothelial cells

被引:0
|
作者
Shu-Er Chow
Wing-Keung Chu
Stephen H. Shih
Jan-Kan Chen
机构
[1] Chang Gung University,Center of General Study
[2] Chang Gung University,Department of Physiology, College of Medicine
[3] National Taiwan Normal University,Department of Biology
关键词
oxidized LDL; endothelial cells; Ras protein; Ras signaling pathway;
D O I
暂无
中图分类号
学科分类号
摘要
Oxidized low-density lipoprotein (ox-LDL) has been shown to alter the migratory and proliferative activities of the vascular endothelial cells (EC) in response to serum and growth factors. The mechanism underlying the antiproliferative effect of ox-LDL on vascular EC has not been fully elucidated. In this report, we show that exposure of vascular EC to ox-LDL results in a marked reduction of the membrane-associated Ras protein. Further study shows that in ox-LDL-treated EC, reduction of the membrane-associated Ras protein is correlated with a reduced amount of active Ras (Ras-guanosine triphosphate), indicating that the Ras signaling pathway is attenuated. The attenuation of the Ras signaling pathway in ox-LDL-treated EC may thus be responsible for the retarded response to the mitogenic stimulation of serum and growth factors.
引用
收藏
页码:320 / 325
页数:5
相关论文
共 50 条
  • [1] Exposure to oxidized low-density lipoprotein reduces activable Ras protein in vascular endothelial cells
    Chow, SE
    Chu, WK
    Shih, SH
    Chen, JK
    IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-ANIMAL, 2002, 38 (06) : 320 - 325
  • [2] Ginkgolide B Reduces Inflammatory Protein Expression in Oxidized Low-density Lipoprotein-stimulated Human Vascular Endothelial Cells
    Zhang, Shan
    Chen, Beidong
    Wu, Wei
    Bao, Li
    Qi, Ruomei
    JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2011, 57 (06) : 721 - 727
  • [3] Impaired lipophagy in endothelial cells with prolonged exposure to oxidized low-density lipoprotein
    Zhang, Cai-Ping
    Ding, Xin-Xin
    Tian, Tian
    Li, Bo-Jie
    Wang, Chu-Yao
    Jiang, Su-Su
    Shao, Jin-Qi
    Yuan, Yu-Lin
    Tian, Ying
    Zhang, Min
    Long, Shi-Yin
    MOLECULAR MEDICINE REPORTS, 2020, 22 (04) : 2665 - 2672
  • [4] Autophagy and Apoptosis in the Response of Human Vascular Endothelial Cells to Oxidized Low-Density Lipoprotein
    Zhang, Yanlin
    Xie, Ying
    You, Shoujiang
    Han, Qiao
    Cao, Yongjun
    Zhang, Xia
    Xiao, Guodong
    Chen, Rui
    Liu, Chunfeng
    CARDIOLOGY, 2015, 132 (01) : 27 - 33
  • [5] An endothelial receptor for oxidized low-density lipoprotein
    Tatsuya Sawamura
    Noriaki Kume
    Takuma Aoyama
    Hideaki Moriwaki
    Hajime Hoshikawa
    Yuichi Aiba
    Takeshi Tanaka
    Soichi Miwa
    Yoshimoto Katsura
    Toru Kita
    Tomoh Masaki
    Nature, 1997, 386 : 73 - 77
  • [6] An endothelial receptor for oxidized low-density lipoprotein
    Sawamura, T
    Kume, N
    Aoyama, T
    Moriwaki, H
    Hoshikawa, H
    Aiba, Y
    Tanaka, T
    Miwa, S
    Katsura, Y
    Kita, T
    Masaki, T
    NATURE, 1997, 386 (6620) : 73 - 77
  • [7] Protein modification elicited by oxidized low-density lipoprotein (LDL) in endothelial cells: Protection by (-)-epicatechin
    Steffen, Yvonne
    Jung, Tobias
    Klotz, Lars-Oliver
    Schewe, Tankred
    Grune, Tilman
    Sies, Helmut
    FREE RADICAL BIOLOGY AND MEDICINE, 2007, 42 (07) : 955 - 970
  • [8] OXIDIZED LOW-DENSITY LIPOPROTEIN STIMULATES PROSTACYCLIN PRODUCTION BY ADULT HUMAN VASCULAR ENDOTHELIAL-CELLS
    TRIAU, JE
    MEYDANI, SN
    SCHAEFER, EJ
    ARTERIOSCLEROSIS, 1988, 8 (06): : 810 - 818
  • [9] Stimulation of NADPH oxidase by oxidized low-density lipoprotein induces proliferation of human vascular endothelial cells
    Heinloth, A
    Heermeier, K
    Raff, U
    Wanner, C
    Galle, J
    JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2000, 11 (10): : 1819 - 1825
  • [10] Nintedanib ameliorates oxidized low-density lipoprotein -induced inflammation and cellular senescence in vascular endothelial cells
    Li, Ling
    Chen, Yudan
    Shi, Chang
    BIOENGINEERED, 2022, 13 (03) : 6196 - 6207