Alterations of arterial physiology in osteopontin-null

被引:41
作者
Myers, DL
Harmon, KJ
Lindner, V
Liaw, L
机构
[1] Maine Med Ctr, Res Inst, Ctr Mol Med, Scarborough, ME 04074 USA
[2] Univ Maine, Orono, ME USA
关键词
osteopontin; cardiovasculature; remodeling; carotid artery; flow cessation;
D O I
10.1161/01.ATV.0000073312.34450.16
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective-In this study, we characterized the effects of an osteopontin (OPN)-null mutation in normal arterial function and remodeling in a murine model. Methods and Results-OPN-null mutant mice were compared with wild-type mice before and after carotid artery ligation. Before ligation, OPN-null mice had increased heart rate, lower blood pressure, and increased circulating lymphocytes compared with wild-type mice. OPN-null vessels also demonstrated greater compliance accompanied by a loosely organized collagen network. After carotid artery ligation, significant differences were also found in the remodeling response of OPN-null animals. At 4 days after ligation, leukocyte adhesion/invasion was diminished by 10-fold in OPN-null mice compared with wild-type mice. At 14 days after ligation, the ligated arteries of OPN-null mice had smaller neointimal lesions but greater constrictive remodeling compared with wild-type mice, resulting in similar lumen areas. Continued remodeling resulted in a similar morphological phenotype in both groups at 28 days. Conclusions-These data show that endogenous OPN regulates normal vascular physiology and contributes to the vascular remodeling response by regulating vascular compliance and the inflammatory response.
引用
收藏
页码:1021 / 1028
页数:8
相关论文
共 75 条
[31]   Endothelial NO synthase overexpression inhibits lesion formation in mouse model of vascular remodeling [J].
Kawashima, S ;
Yamashita, T ;
Ozaki, M ;
Ohashi, Y ;
Azumi, H ;
Inoue, N ;
Hirata, K ;
Hayashi, Y ;
Itoh, H ;
Yokoyama, M .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2001, 21 (02) :201-207
[32]   Mapping of functional epitopes of osteopontin by monoclonal antibodies raised against defined internal sequences [J].
Kon, S ;
Yokosaki, Y ;
Maeda, M ;
Segawa, T ;
Horikoshi, Y ;
Tsukagoshi, H ;
Rashid, MM ;
Morimoto, J ;
Inobe, M ;
Shijubo, N ;
Chambers, AF ;
Uede, T .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2002, 84 (02) :420-432
[33]  
Kumar A, 1997, CIRCULATION, V96, P4333
[34]   Remodeling with neointima formation in the mouse carotid artery after cessation of blood flow [J].
Kumar, A ;
Lindner, V .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1997, 17 (10) :2238-2244
[35]   Local pulse pressure is a major determinant of large artery remodelling [J].
Laurent, S ;
Tropeano, AI ;
Lillo-Lelouet, A ;
Jondeau, G ;
Laloux, B ;
Boutouyrie, P .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2001, 28 (12) :1011-1014
[36]   Smooth muscle cells of the media in the dilatative pathology of ascending thoracic aorta: Morphology, immunoreactivity for osteopontin, matrix metalloproteinases, and their inhibitors [J].
Lesauskaite, V ;
Tanganelli, P ;
Sassi, C ;
Neri, E ;
Diciolla, F ;
Ivanoviene, L ;
Epistolato, MC ;
Lalinga, AV ;
Alessandrini, C ;
Spina, D .
HUMAN PATHOLOGY, 2001, 32 (09) :1003-1011
[37]   Novel arterial pathology in mice and humans hemizygous for elastin [J].
Li, DY ;
Faury, G ;
Taylor, DG ;
Davis, EC ;
Boyle, WA ;
Mecham, RP ;
Stenzel, P ;
Boak, B ;
Keating, MT .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (10) :1783-1787
[38]   Neutralizing antibodies directed against osteopontin inhibit rat carotid neointimal thickening after endothelial denudation [J].
Liaw, L ;
Lombardi, DM ;
Almeida, MM ;
Schwartz, SM ;
deBlois, D ;
Giachelli, CM .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1997, 17 (01) :188-193
[39]   OSTEOPONTIN AND BETA(3) INTEGRIN ARE COORDINATELY EXPRESSED IN REGENERATING ENDOTHELIUM IN-VIVO AND STIMULATE ARG-GLY-ASP-DEPENDENT ENDOTHELIAL MIGRATION IN-VITRO [J].
LIAW, L ;
LINDNER, V ;
SCHWARTZ, SM ;
CHAMBERS, AF ;
GIACHELLI, CM .
CIRCULATION RESEARCH, 1995, 77 (04) :665-672
[40]   OSTEOPONTIN PROMOTES VASCULAR CELL-ADHESION AND SPREADING AND IS CHEMOTACTIC FOR SMOOTH-MUSCLE CELLS IN-VITRO [J].
LIAW, L ;
ALMEIDA, M ;
HART, CE ;
SCHWARTZ, SM ;
GIACHELLI, CM .
CIRCULATION RESEARCH, 1994, 74 (02) :214-224