| Project/Area Number |
08670795
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Circulatory organs internal medicine
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| Research Institution | Shimane Medical University |
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Principal Investigator |
MASUDA Junichi Shimane Medical University, Department of Laboratory Medicine, Professor, 医学部, 教授 (70173747)
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| Co-Investigator(Kenkyū-buntansha) |
ABUMIYA Takeo National Cardiovascular Center, Research staff, 室員 (80270726)
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| Project Period (FY) |
1996 – 1997
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| Project Status |
Completed (Fiscal Year 1997)
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| Budget Amount *help |
¥2,200,000 (Direct Cost: ¥2,200,000)
Fiscal Year 1997: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1996: ¥1,400,000 (Direct Cost: ¥1,400,000)
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| Keywords | stent / macrophage / smoothh muscle cell / extracellular matrix / decorin / biglycan / cytokine / hypertension / 血管壊死 / 動脈硬化 / 組織適合性抗原 / 血管形成術 |
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| Research Abstract |
1.Leucine-rich small proteoglycans, decorin and biglycan, which can bind to TGF-beta, are considered to participate in regulation of extracellular matrix accumulation in arterial intimal hyperplasia. To investigate their correlation with the cellular localization and phenotypic modulation of smooth muscle cells, we analyzed the spatial and chronological distribution of these proteoglycans and two cytokines in the process of neointima formation after stent implantation in aortas of rabbits fed on both high-cholesterol chow (atherosclerotic group) and regular one (control group). We implanted Gianturco's Z type stents in the rabbit aortas and harvested the aortas at day 4-56 days for immunohistochemical and in situ hybridization analysis. The results supprted that the biglycan and decorin kinetics during neointima formation after arterial injury are distinct in spite of their similar construction ; biglycan synthesis correlates with the embryonic smooth muscle cells, whereas decorin synthesis is accelerated by IL-1betasecreted from macrophages accumulating in the injured areas in the late stage after the vascular injury.
2.In hypertensive vascular lesions, various pathologic changes are exhibited. To clarify the mechanisms responsible for this diversity of vascular lesions, we immunohistochemically examined hypertensive vascular lesions in stroke-prone spontaneously hypertensive rats with reference to the distribution of macrophage subsets. The results suggest that heterogeneity in the time course of macrophage infiltration and inthe distribution of macrophage subsets among the vascular tres of various organs seems to be correlated with the diversity of hypertensive vascular lesions. Differences in the routes that supply macrophages and their functions may determine the pathologic changes in the vascular lesions.
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