Normalization of high-flow or removal of flow cannot stop high-flow induced endothelial proliferation
被引:3
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作者:
Yamauchi, Misa
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机构:Akita Univ, Sch Med, Dept Pathol & Immunol, Div Cellular & Organ Pathol, Akita 0108543, Japan
Yamauchi, Misa
Takahashi, Masato
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机构:Akita Univ, Sch Med, Dept Pathol & Immunol, Div Cellular & Organ Pathol, Akita 0108543, Japan
Takahashi, Masato
Kobayashi, Mikio
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机构:Akita Univ, Sch Med, Dept Pathol & Immunol, Div Cellular & Organ Pathol, Akita 0108543, Japan
Kobayashi, Mikio
Sho, Eiketsu
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机构:Akita Univ, Sch Med, Dept Pathol & Immunol, Div Cellular & Organ Pathol, Akita 0108543, Japan
Sho, Eiketsu
Nanjo, Hiroshi
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机构:Akita Univ, Sch Med, Dept Pathol & Immunol, Div Cellular & Organ Pathol, Akita 0108543, Japan
Nanjo, Hiroshi
Kawamura, Kouichi
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机构:Akita Univ, Sch Med, Dept Pathol & Immunol, Div Cellular & Organ Pathol, Akita 0108543, Japan
Kawamura, Kouichi
Masuda, Hirotake
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机构:
Akita Univ, Sch Med, Dept Pathol & Immunol, Div Cellular & Organ Pathol, Akita 0108543, JapanAkita Univ, Sch Med, Dept Pathol & Immunol, Div Cellular & Organ Pathol, Akita 0108543, Japan
Masuda, Hirotake
[1
]
机构:
[1] Akita Univ, Sch Med, Dept Pathol & Immunol, Div Cellular & Organ Pathol, Akita 0108543, Japan
[2] Stanford Univ, Dept Surg, Sch Med, Stanford, CA 94305 USA
[3] Akita Univ Hosp, Div Clin Pathol, Akita, Japan
来源:
BIOMEDICAL RESEARCH-TOKYO
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2005年
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26卷
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01期
关键词:
D O I:
10.2220/biomedres.26.21
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
Endothelial cells (ECs) are activated in response to high-flow. Our previous studies using arteriovenous fistula (AVF) model have demonstrated that high-flow in blood vessels induces an early and rapid proliferation of ECs before arterial dilatation. Here, we investigated the proliferation of ECs, which had once been stimulated by high-flow loading, in a situation without the influence of high-flow. First, we induced high-flow in the rabbit common carotid artery by using AVF Then, we removed the influence of high-flow by normalization of high-flow with the closure of AVF or by removal of flow itself with tissue isolation and organ culture or with cell culture of ECs, at the timing considered that ECs began to proliferate. Kinetics of ECs was investigated by a laser scanning confocal microscopy, phase-contrast microscopy and light microscopy using bromodcoxyuridine labeling method. We found that ECs, which had once been stimulated by high-flow, transiently proliferated even after normalization of high-flow or removal of flow. We assume that proliferation of ECs is promised when these cells start to proliferate after high-flow loading.