HISTAMINE AS AN ACTIVATOR OF CELL-GROWTH AND EXTRACELLULAR-MATRIX RECONSTRUCTION FOR HUMAN VASCULAR SMOOTH-MUSCLE CELLS

被引:39
作者
SATOH, T
SUGAMA, K
MATSUO, A
KATO, S
ITO, S
HATANAKA, M
SASAGURI, Y
机构
[1] BAYER YAKUHIN LTD,INST PHARMACOL,DEPT ALLERGY CELL BIOL,NISHI KU,KOBE 65123,JAPAN
[2] KURUME UNIV,SCH MED,DEPT PATHOL,KURUME,FUKUOKA 830,JAPAN
[3] OSAKA BIOSCI INST,DEPT CELL BIOL,SUITA,OSAKA 565,JAPAN
[4] KYOTO UNIV,INST VIRUS RES,DEPT HUMAN RETROVIRUS,SAKYO KU,KYOTO 606,JAPAN
[5] UNIV OCCUPAT & ENVIRONM HLTH,DEPT PATHOL,NISHI KU,KITAKYUSHU,FUKUOKA 807,JAPAN
关键词
HISTAMINE; ATHEROSCLEROSIS; CONNECTIVE TISSUE DEGRADATION; ISS10; SMOOTH MUSCLE CELLS;
D O I
10.1016/0021-9150(94)90067-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Atherosclerosis is characterised by unusual growth of vascular smooth muscle cells (VSMCs) in the intima. We examined the effects of histamine on human VSMCs and the VSMC-derived cell line, ISS10. Histamine enhanced phosphoinositide hydrolysis, increased cytoplasmic Ca2+ level and stimulated the transcription of c-fos protooncogene, which resulted in DNA synthesis and the enhancement of proMMP-1 expression. These results indicate that histamine may play some roles in the pathological process of atherosclerosis and raise the possibility that mast cells migrating into the atherosclerotic foci are involved in the process of atherosclerogenesis.
引用
收藏
页码:53 / 61
页数:9
相关论文
共 47 条
[1]   PHORBOL ESTER INDUCIBLE GENES CONTAIN A COMMON CIS ELEMENT RECOGNIZED BY A TPA-MODULATED TRANS-ACTING FACTOR [J].
ANGEL, P ;
IMAGAWA, M ;
CHIU, R ;
STEIN, B ;
IMBRA, RJ ;
RAHMSDORF, HJ ;
JONAT, C ;
HERRLICH, P ;
KARIN, M .
CELL, 1987, 49 (06) :729-739
[2]   AUTO-INHIBITION OF BRAIN HISTAMINE-RELEASE MEDIATED BY A NOVEL CLASS (H-3) OF HISTAMINE-RECEPTOR [J].
ARRANG, JM ;
GARBARG, M ;
SCHWARTZ, JC .
NATURE, 1983, 302 (5911) :832-837
[3]   THE ASSOCIATION OF MAST-CELLS AND ATHEROSCLEROSIS - A MORPHOLOGIC STUDY OF EARLY ATHEROSCLEROTIC LESIONS IN YOUNG-PEOPLE [J].
ATKINSON, JB ;
HARLAN, CW ;
HARLAN, GC ;
VIRMANI, R .
HUMAN PATHOLOGY, 1994, 25 (02) :154-159
[4]  
BARTHOLEYNS J, 1985, TRENDS PHARMACOL SCI, V7, P123
[5]   CHANGES IN THE LEVELS OF INOSITOL PHOSPHATES AFTER AGONIST-DEPENDENT HYDROLYSIS OF MEMBRANE PHOSPHOINOSITIDES [J].
BERRIDGE, MJ ;
DAWSON, RMC ;
DOWNES, CP ;
HESLOP, JP ;
IRVINE, RF .
BIOCHEMICAL JOURNAL, 1983, 212 (02) :473-482
[6]   INOSITOL TRISPHOSPHATE, A NOVEL 2ND MESSENGER IN CELLULAR SIGNAL TRANSDUCTION [J].
BERRIDGE, MJ ;
IRVINE, RF .
NATURE, 1984, 312 (5992) :315-321
[7]   PRESENCE OF EPIDERMAL GROWTH-FACTOR RECEPTORS AND INFLUENCE OF EPIDERMAL GROWTH-FACTOR ON PROLIFERATION AND AGING IN CULTURED SMOOTH-MUSCLE CELLS [J].
BHARGAVA, G ;
RIFAS, L ;
MAKMAN, MH .
JOURNAL OF CELLULAR PHYSIOLOGY, 1979, 100 (02) :365-374
[8]  
BLAUCHARD JM, 1985, NATURE, V317, P443
[9]   MYOPLASMIC CA-2+-FORCE RELATIONSHIP STUDIED WITH FURA-2 DURING STIMULATION OF RAT AORTIC SMOOTH-MUSCLE [J].
BRUSCHI, G ;
BRUSCHI, ME ;
REGOLISTI, G ;
BORGHETTI, A .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 254 (05) :H840-H854
[10]   DIFFERENTIAL STIMULATION OF COLLAGENASE AND CHEMOTACTIC ACTIVITY IN FIBROBLASTS DERIVED FROM RAT WOUND REPAIR TISSUE AND HUMAN-SKIN BY GROWTH-FACTORS [J].
BUCKLEYSTURROCK, A ;
WOODWARD, SC ;
SENIOR, RM ;
GRIFFIN, GL ;
KLAGSBRUN, M ;
DAVIDSON, JM .
JOURNAL OF CELLULAR PHYSIOLOGY, 1989, 138 (01) :70-78