Project/Area Number |
63570144
|
Research Category |
Grant-in-Aid for General Scientific Research (C)
|
Allocation Type | Single-year Grants |
Research Field |
Human pathology
|
Research Institution | Saga Medical School |
Principal Investigator |
WATANABE Teruo Saga Medical School, Pathology Professor, 医学部, 教授 (40037396)
|
Co-Investigator(Kenkyū-buntansha) |
SHIMOKAMA Tatsuro Saga Medical School Assistant, 医学部, 助手 (50170999)
YOSHIKAWA Yasuji Saga Medical School, Pathology Assistant, 医学部, 助手 (80124816)
|
Project Period (FY) |
1988 – 1989
|
Project Status |
Completed (Fiscal Year 1989)
|
Budget Amount *help |
¥2,200,000 (Direct Cost: ¥2,200,000)
Fiscal Year 1989: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 1988: ¥1,700,000 (Direct Cost: ¥1,700,000)
|
Keywords | Atherosclerosis / Macrophage / Foam cell / Lymphocyte / Hypercholesterolemia / Lipoprotein / Hypertension / Cerebral Atherosclerosis / マクロファージ / 高コレステロール血症 / 発生病理 |
Research Abstract |
1. To investigate the role of macrophages and lymphocytes in human atherosclerosis, immunohistological methods combined with electron microscopic analysis were used to assess the cellular infiltrates in human arterial intima such as normal areas on gross inspection, fatty streaks and atheromatous plaques. In the lesions of fatty streaks and atheromatous plaques including the fibrous cap and shoulder region, OKM1+ LeuM3+ macrophages as well as macrrophage foam cells were intimately coexisted with OKT3+ lymphocytes. It was worthy to note that such colocalization of macrophages and T lymphocytes was detectable in some areas of grossly normal intima. Electron microscopy demonstrated the direct cellular contact not only between lymphocytes and macrophages but also among lymphocyte-lymphocyte and macrophage-macrophage. 2. To assess the development and initial lesion sites of cerebral atherosclerosis in rabbits, the dorsal surface of the cerebral artery segment covering from the vertebral arteries to posterior cerebral arteries was thoroughly examined by scanning microscopy. The results showed that hypertension coupled with hypercholesterolemia induced atherosclerosis in certain vulnerable regions of the cerebral arteries. 3. Interaction of macrophages with cultured endothelila cells was studied. Pretreatment with LDL and VLDL increased adhesion of macrophages to endothelial cells. Macrophages from hypercholesterolemic animals showed enhanced attachment to the endothelila cells; they moved more quickly when examined by time-lapse cinephotomicrography. 4. We produced an in vitro model of a blood vessel wall consisting of human umbilical vein endothelial cells cultured on human amnion.
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