Does the coronary risk factor low density lipoprotein alter growth and signaling in vascular smooth muscle cells?

被引:22
作者
Gouni-Berthold, I
Sachinidis, A
机构
[1] Univ Cologne, Ctr Physiol & Pathophysiol, D-50931 Cologne, Germany
[2] Univ Cologne, Med Clin 2, D-50931 Cologne, Germany
关键词
LDL; atherosclerosis; hypertension; signal transduction; MAP kinases; sphingosine-1; phosphate;
D O I
10.1096/fj.02-0260rev
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
There is increasing evidence that hypertension promotes low density lipoprotein (LDL) transportation into the subendothelial space of the vascular wall. Vascular smooth muscle cell (VSMC) proliferation plays an important role in the development and progression of cardiovascular diseases. Recently, several studies have demonstrated that LDL acts as a classic growth factor promoting VSMC growth via mitogenic signals normally elicited by classic growth factors. The present work summarizes current nontraditional concepts regarding possible cellular mechanisms through which hypertension and LDL may promote the development of atherosclerosis. Especially addressed are the possible effects of an elevated blood pressure in combination with LDL on VSMC growth. The new research concept concerning LDL as a growth factor and carrier for biological active phospholipids such as sphingosine-1-phosphate and sphingosylphosphorylcholine may contribute to an understanding of the pathogenesis of atherosclerosis by elevated high blood pressure.
引用
收藏
页码:1477 / 1487
页数:11
相关论文
共 158 条
[1]   A Ras-dependent pathway regulates RNA polymerase II phosphorylation in cardiac myocytes: Implications for cardiac hypertrophy [J].
Abdellatif, M ;
Packer, SE ;
Michael, LH ;
Zhang, D ;
Charng, MJ ;
Schneider, MD .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (11) :6729-6736
[2]   Influence of plasma lipid and LDL-subfraction profile on the interaction between low density lipoprotein with human arterial wall proteoglycans [J].
Anber, V ;
Griffin, BA ;
McConnell, M ;
Packard, CJ ;
Shepherd, J .
ATHEROSCLEROSIS, 1996, 124 (02) :261-271
[3]   BINDING OF SH2 DOMAINS OF PHOSPHOLIPASE-C-GAMMA-1, GAP, AND SRC TO ACTIVATED GROWTH-FACTOR RECEPTORS [J].
ANDERSON, D ;
KOCH, CA ;
GREY, L ;
ELLIS, C ;
MORAN, MF ;
PAWSON, T .
SCIENCE, 1990, 250 (4983) :979-982
[4]   The sphingomyelin-ceramide signaling pathway is involved in oxidized low density lipoprotein-induced cell proliferation [J].
Auge, N ;
Andrieu, N ;
NegreSalvayre, A ;
Thiers, JC ;
Levade, T ;
Salvayre, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (32) :19251-19255
[5]   Role of sphingosine 1-phosphate in the mitogenesis induced by oxidized low density lipoprotein in smooth muscle cells via activation of sphingomyelinase, ceramidase, and sphingosine kinase [J].
Augé, N ;
Nikolova-Karakashian, M ;
Carpentier, S ;
Parthasarathy, S ;
Négre-Salvayre, A ;
Salvayre, R ;
Merrill, AH ;
Levade, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (31) :21533-21538
[6]   PROLIFERATIVE AND CYTOTOXIC EFFECTS OF MILDLY OXIDIZED LOW-DENSITY LIPOPROTEINS ON VASCULAR SMOOTH-MUSCLE CELLS [J].
AUGE, N ;
PIERAGGI, MT ;
THIERS, JC ;
NEGRESALVAYRE, A ;
SALVAYRE, R .
BIOCHEMICAL JOURNAL, 1995, 309 :1015-1020
[7]   OXIDIZED LOW-DENSITY-LIPOPROTEIN IS CHEMOTACTIC FOR ARTERIAL SMOOTH-MUSCLE CELLS IN CULTURE [J].
AUTIO, I ;
JAAKKOLA, O ;
SOLAKIVI, T ;
NIKKARI, T .
FEBS LETTERS, 1990, 277 (1-2) :247-249
[8]   Minimally modified low density lipoproteins induce aortic smooth muscle cell proliferation via the activation of mitogen activated protein kinase [J].
Balagopalakrishna, C ;
Bhunia, AK ;
Rifkind, JM ;
Chatterjee, S .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1997, 170 (1-2) :85-89
[9]   Redox-regulated signaling by lactosylceramide in the proliferation of human aortic smooth muscle cells [J].
Bhunia, AK ;
Han, H ;
Snowden, A ;
Chatterjee, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (25) :15642-15649
[10]   Lactosylceramide stimulates Ras-GTP loading, kinases (MEK, Raf), p44 mitogen-activated protein kinase, and c-fos expression in human aortic smooth muscle cells [J].
Bhunia, AK ;
Han, H ;
Snowden, A ;
Chatterjee, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (18) :10660-10666