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Are there differences among characteristics of portions of human mesenteric artery trees?

Are there differences among characteristics of portions of human mesenteric artery trees?
人类肠系膜动脉树各部分的特征是否存在差异?
批准号:
10670153
负责人:
GOTO Kunihiko
金额:
$1.86万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1998
资助国家:
日本
项目状态:
已结题
起止时间:
1998 至 1999

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中文摘要
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英文摘要
Vascular lesion formations in such disease states as hypertension and atherosclerosis occur in a district-specific manner. Large conduit and small resistance arteries play district-specific roles in the regulation of organ perfusion. Using a culture method, we studied the morphology and growth of smooth muscle cells derived from small arteries (S-SMCs, less than 90μm in internal diameter) and from larger arteries (L-SMCs, ranging from 800 to 900μm) of the rat mesenteric arterial bed. S-SMCs were smaller, bipolar-shaped ; in contrast, the majority of L-SMCs were larger, polygonal-shaped. Actin fibers within S-SMCs were oriented in a bipolar manner from the nuclei, whereas those within L-SMCs had a radial appearance. [3H]Thymidine incorporation induced by serum, platelet-derived growth factor-AB(PDGF), or mechanical stretch was greater in S- vs L-SMCs. The population doubling time measured after the addition of serum or PDGF was shorter in S- vs L-SMCs. Thus, distinct morphological and growth phenotypes of SMCs exist in small and larger arteries of the same vascular bed.Furthermore, we clarified that there are the same relationship between S- and L-SMCs in smooth muscle cells of human mesenteric arteries and furthermore that there are differences among characteristics of portions of human mesenteric artery trees using differentiation markers of calponin and caldesmon, and receptors of endotherins and angiotensins in addition of intermediated size filaments.
期刊论文(6)
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会议论文
Nakamura A. et al.: "Vessel size-dependent expression of intermediate-sized filaments,calponin and h-caldesmon in smooth muscle cells of human coronary arteries" Cordiovascular Research. (in press). (1999)
Nakamura A. 等人:“人冠状动脉平滑肌细胞中中等大小的丝、钙调蛋白和 h-caldesmon 的血管大小依赖性表达”心血管研究。
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通讯作者:
Goto, K.: "Rotation model - A molecular mechanism driven by hydrophobic and hydrophilic interactions, and underlying molecular recognition and ion channels -"Progress in Anesthetic Mechanism. 5. 1-22 (1997)
Goto, K.:“旋转模型 - 由疏水性和亲水性相互作用驱动的分子机制,以及潜在的分子识别和离子通道 -”麻醉机制的进展。
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後藤邦彦: "回転モデル―nAChR、麻酔作用、酵素触媒作用、免疫ジグナル伝達などの分子機構を解明・予測する分子仮説―"臨床麻酔. 23. 157-164 (1999)
Kunihiko Goto:“旋转模型 - 阐明和预测 nAChR、麻醉、酶催化、免疫信号传递等分子机制的分子假说” 23. 157-164 (1999)。
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通讯作者:
Nakamura A. et al.: "Heterogeneous smooth muscle cell population derived from small and carge arteries" Microvascular Research. 55. 14-28 (1998)
Nakamura A. 等人:“源自小动脉和大动脉的异质平滑肌细胞群”微血管研究。
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    • 资助金额:
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