INVOLVEMENT OF LDL RECEPTOR IN THE PROLIFERATION OF VASCULAR SMOOTH-MUSCLE CELLS

被引:18
作者
IKEDA, U
OGUCHI, A
OKADA, K
ISHIKAWA, S
SAITO, T
IKEDA, M
KANO, S
TAKAHASHI, M
SHIOMI, M
SHIMADA, K
机构
[1] JICHI MED SCH,DEPT ENDOCRINOL & METAB,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
[2] JICHI MED SCH,DEPT CLIN IMMUNOL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
[3] UTSUNOMIYA UNIV,CTR HLTH SCI,UTSUNOMIYA,TOCHIGI,JAPAN
[4] KOBE UNIV,SCH MED,INST EXPTL ANIM,KOBE,HYOGO,JAPAN
关键词
ATHEROSCLEROSIS; HYPERLIPIDEMIA; DNA SYNTHESIS; MAP KINASE;
D O I
10.1016/0021-9150(94)90071-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To study the involvement of the low-density lipoprotein (LDL) receptor in the growth of vascular smooth muscle cells (VSMC), we compared the proliferation of cultured VSMC from Watanabe heritable hyperlipidemic (WHHL) rabbits, which lack the LDL receptor, and VSMC from normal Japanese white rabbits in response to platelet derived growth factor (PDGF), The increase in the number of VSMC from WHHL rabbits in response to PDGF (10(-8) M) was significantly lower than that of VSMC from normal rabbits. PDGF stimulated the synthesis of DNA in VSMC from both normal rabbits and WHHL rabbits, but the response was significantly lower in the latter. To determine the involvement of the LDL receptor in the decreased mitogenic response of WHHL rabbit VSMC, we used an anti-LDL receptor monoclonal antibody (MAb) to normal rabbit VSMC; DNA synthesis of VSMC was stimulated by PDGF, but the effect was significantly blocked by the anti-LDL receptor MAb. Mitogen-activated protein (MAP) kinase activity in normal rabbit VSMC was increased by exposure to PDGF, but the effect was significantly suppressed in the presence of the MAb. The anti-LDL receptor MAb markedly inhibited LDL binding to the surface of normal rabbit VSMC. These results suggest that the LDL receptor influences the proliferation of VSMC and thus might be involved in the pathogenesis of atherosclerosis.
引用
收藏
页码:87 / 94
页数:8
相关论文
共 29 条
[1]  
ALVAREZ E, 1991, J BIOL CHEM, V266, P15277
[2]   EFFECT OF LIPOPROTEIN ON INVITRO SYNTHESIS OF DNA IN AORTIC TISSUE [J].
AUGUSTYN, JM ;
FRITZ, KE ;
DAOUD, AS ;
JARMOLYCH, J .
ATHEROSCLEROSIS, 1977, 27 (02) :179-188
[3]   METABOLISM OF VERY LOW-DENSITY LIPOPROTEIN PROTEINS .1. PRELIMINARY IN-VITRO AND IN-VIVO OBSERVATIONS [J].
BILHEIMER, DW ;
LEVY, RI ;
EISENBERG, S .
BIOCHIMICA ET BIOPHYSICA ACTA, 1972, 260 (02) :212-+
[4]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[5]   RECENT ADVANCES IN MOLECULAR PATHOLOGY - SMOOTH-MUSCLE PHENOTYPIC CHANGES IN ARTERIAL-WALL HOMEOSTASIS - IMPLICATIONS FOR THE PATHOGENESIS OF ATHEROSCLEROSIS [J].
CAMPBELL, GR ;
CAMPBELL, JH .
EXPERIMENTAL AND MOLECULAR PATHOLOGY, 1985, 42 (02) :139-162
[6]  
CAMPBELL JHC, 1981, ATHEROSCLEROSIS, V40, P347
[7]   PLATELET-DERIVED GROWTH-FACTOR STIMULATES ACTIVITY OF LOW-DENSITY LIPOPROTEIN RECEPTORS [J].
CHAIT, A ;
ROSS, R ;
ALBERS, JJ ;
BIERMAN, EL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (07) :4084-4088
[8]  
ECSEDI GG, 1986, METHOD FIND EXP CLIN, V8, P535
[9]  
FISHERDZOGA K, 1976, ATHEROSCLEROSIS, V24, P515
[10]  
GERRITY RG, 1981, AM J PATHOL, V103, P191