Expression of cytokine and adhesion molecule mRNA in atherectomy specimens from patients with coronary artery disease

被引:15
作者
Ishibashi, T
Kijima, M
Yokoyama, K
Shindo, J
Nagata, K
Hirosaka, A
Techigawara, M
Abe, Y
Sato, E
Yamaguchi, N
Watanabe, N
Saito, T
Maehara, K
Ohmoto, Y
Maruyama, Y
机构
[1] Fukushima Med Univ, Dept Internal Med 1, Fukushima 96012, Japan
[2] Hoshi Gen Hosp, Ctr Cardiovasc, Koriyama, Fukushima, Japan
[3] Ohta Nishinouchi Gen Hosp, Div Cardiol, Koriyama, Fukushima, Japan
[4] Ohara Med Ctr, Div Cardiol, Fukushima, Japan
[5] Otsuka Pharmaceut Co Ltd, Tokushima 77101, Japan
来源
JAPANESE CIRCULATION JOURNAL-ENGLISH EDITION | 1999年 / 63卷 / 04期
关键词
adhesion molecules; arteriosclerosis; coronary artery disease; cytokines;
D O I
10.1253/jcj.63.249
中图分类号
N09 [自然科学史]; B [哲学、宗教];
学科分类号
01 ; 0101 ; 010108 ; 060207 ; 060305 ; 0712 ;
摘要
Coronary arteriosclerosis is an underlying condition in acute myocardial infarction (AMI), unstable angina pectoris (UAP) and stable angina pectoris (SAP), and is also related to restenosis (RS) following coronary intervention. To investigate the pathogenesis of this condition, a quantitative reverse transcriptase polymerase chain reaction was used to determine relative levels of mRNA for interleukin (IL)-1 beta, IL-6, IL-8, transforming growth factor beta (TGF-beta), intercellular adhesion molecule (ICAM)-1, E-selectin and vascular cell adhesion molecule (VCAM)-1 using directional coronary atherectomy (DCA) specimens. Eleven patients with AMI, 7 with UAP, 10 with SAP and 6 with RS following a previous coronary intervention underwent DCA. The mRNA intensity for each molecule was expressed by comparing it with that of p-actin mRNA. The AMI and UAP patients showed high frequencies of mRNA for IL-1 beta, IL-8, TGF-P, and ICAM-1 together with strong intensities of expression, whereas SAP patients showed decreased mRNA expression for these molecules. Increased IL-6 mRNA expression was observed only in AMI samples. Specimens from RS patients revealed an accumulated expression of proinflammatory cytokines, except for IL-6, as well as of TGF-beta. The study suggests that variation in mRNA expression may reflect the pathophysiology of specific types of coronary artery disease, and remodeling following vascular injury.
引用
收藏
页码:249 / 254
页数:6
相关论文
共 27 条
[1]   PROBLEMS IN THE DEVELOPMENT OF NEW DEVICES FOR CORONARY INTERVENTION - POSSIBLE ROLE FOR A MULTICENTER REGISTRY [J].
BAIM, DS ;
DETRE, K ;
KENT, K .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1989, 14 (05) :1389-1392
[2]   UNSTABLE ANGINA - A CLASSIFICATION [J].
BRAUNWALD, E .
CIRCULATION, 1989, 80 (02) :410-414
[3]   REGULATION OF VASCULAR CELL-ADHESION MOLECULE-1 AND INTERCELLULAR-ADHESION MOLECULE-1 IN HUMAN VASCULAR SMOOTH-MUSCLE CELLS [J].
COUFFINHAL, T ;
DUPLAA, C ;
MOREAU, C ;
LAMAZIERE, JMD ;
BONNET, J .
CIRCULATION RESEARCH, 1994, 74 (02) :225-234
[4]   RELATION OF STENOSIS MORPHOLOGY AND CLINICAL PRESENTATION TO THE PROCEDURAL RESULTS OF DIRECTIONAL CORONARY ATHERECTOMY [J].
ELLIS, SG ;
DECESARE, NB ;
PINKERTON, CA ;
WHITLOW, P ;
KING, SB ;
GHAZZAL, ZMB ;
KEREIAKES, DJ ;
POPMA, JJ ;
MENKE, KK ;
TOPOL, EJ ;
HOLMES, DR .
CIRCULATION, 1991, 84 (02) :644-653
[5]   MECHANISMS OF DISEASE - THE PATHOGENESIS OF CORONARY-ARTERY DISEASE AND THE ACUTE CORONARY SYNDROMES .1. [J].
FUSTER, V ;
BADIMON, L ;
BADIMON, JJ ;
CHESEBRO, JH .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 326 (04) :242-250
[6]   RESTENOSIS AFTER DIRECTIONAL CORONARY ATHERECTOMY - DIFFERENCES BETWEEN PRIMARY ATHEROMATOUS AND RESTENOSIS LESIONS AND INFLUENCE OF SUBINTIMAL TISSUE RESECTION [J].
GARRATT, KN ;
HOLMES, DR ;
BELL, MR ;
BRESNAHAN, JF ;
KAUFMANN, UP ;
VLIETSTRA, RE ;
EDWARDS, WD .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1990, 16 (07) :1665-1671
[7]  
HASSON GK, 1989, ARTERIOSCLEROSIS, V9, P567
[8]   EFFECT OF LESION CHARACTERISTICS ON OUTCOME OF DIRECTIONAL CORONARY ATHERECTOMY [J].
HINOHARA, T ;
ROWE, MH ;
ROBERTSON, GC ;
SELMON, MR ;
BRADEN, L ;
LEGGETT, JH ;
VETTER, JW ;
SIMPSON, JB .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1991, 17 (05) :1112-1120
[9]   CELL-ADHESION MOLECULES IN CORONARY-ARTERY DISEASE [J].
JANG, YS ;
LINCOFF, AM ;
PLOW, EF ;
TOPOL, EJ .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1994, 24 (07) :1591-1601
[10]  
LIBBY P, 1990, ATHER REV, V21, P79