Three-dimensional ultrastructural study of Endothelial cells and pericytes interdigitation in angiogenesis
Three-dimensional ultrastructural study of Endothelial cells and pericytes interdigitation in angiogenesis
批准号:
21580371
负责人:
WAKUI Shin
金额:
$3.24万
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:
2009
资助国家:
日本
项目状态:
已结题
起止时间:
2009 至 2012
中文摘要
血管内皮细胞和周细胞通过血管生成素系统在血管生成中起关键作用。内皮细胞和周细胞交错(EPI)由周细胞的胞质突起和相应的内皮凹陷组成,常见于血管生成部位。大鼠皮下植入一种热可逆凝胶聚合物盘,在体外24-72小时内进行实验。毛细血管密度在48h达到高峰。观察到大量的EPI在72小时达到高峰。连续切片免疫组织化学分析显示,血管生成素-1定位于周细胞和外周细胞。定量RT-PCR分析显示,血管生成素-1水平在72小时后升高。本研究表明微血管成熟可能参与了EPI和Angiopoietin-1的表达。
英文摘要
Endothelial cells and pericytes play critical role in angiogenesis by the angiopoietin system. Endothelial cell and pericyte interdigitations (EPI), consisting of cytoplasmic projections of pericytes and corresponding endothelial indentations, are frequently present at angiogenic sites. Rats subcutaneous implantation of a thermoreversible gelation polymer discs were inqubated in vitro 24-72hr. The capillary density increased to a peak on 48hr. A number of EPI were observed to a peak on 72hr. Serial sectioning electron microscopy immunohistochemical analysis revealed that Angiopoietin-1 localized at Pericytes and EPI. Quantitative RT-PCR analysis revealed that the level of Angiopoietin-1 increased on 72hr. The present study showed that the microvesselmaturation might to be involved in the expression of EPI and Angiopoietin-1.
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Human drug transporter gene-expressing cells are useful alternatives to predictpharmacokinetics in man
人类药物转运蛋白基因表达细胞是预测人类药代动力学的有用替代品
DOI:
--
发表时间:
2011
期刊:
AATEX
影响因子:
--
作者:
[Anzai, N., Wakui, S., Jutabha, P., Muto, T., Hayashi, M., Hayashi, K., Domae, M.,Uchida, K., Wempe, M.F. and Endou, H]
通讯作者:
H
Invitro thermoreversible gel disc quantitative assay of rat angiogenesis
大鼠血管生成的体外热可逆凝胶盘定量分析
DOI:
--
发表时间:
2011
期刊:
AATEX
影响因子:
--
作者:
[Wakui, S., et al]
通讯作者:
et al
LAT1 antagonists suppressed N-methyl-N'- nitrosoguanidine induced rat gastric carcinogenesis
LAT1拮抗剂抑制N-甲基-N-亚硝基胍诱导的大鼠胃癌发生
DOI:
--
发表时间:
2010
期刊:
J. Toxicol. Pathol
影响因子:
--
作者:
[Ishida, K., Muto, T., Motohashi, M.,Kobayashi, Y., Imai, K. and Wakui, S]
通讯作者:
S
Mrophometorical analysis on preneoplastic cellular nuclei in BBN induced rat bladder carcinogenesis
BBN诱导大鼠膀胱癌发生前细胞核的形态学分析
DOI:
--
发表时间:
2012
期刊:
J. Toxicol. Pathol
影响因子:
--
作者:
[Wakui, S., Mtohashi, M., Imai,K.,Kobayashi, Y., Tanaka, I., Nishimoto, T., Sato, T., Muto, T., Takahashi, H. and Hano, H]
通讯作者:
H
Potent hURAT1 inhibitors: in vitro and in vivo metabolism and pharmacokineticstudies
有效的 hURAT1 抑制剂:体外和体内代谢和药代动力学研究
DOI:
--
发表时间:
2011
期刊:
Drug Design, Develop, Therapy
影响因子:
--
作者:
[Wempe, M.F., Rice, P.J., Lightner, J.W., Jutabha, P., Hayashi, M., Anzai, N., Wakui,S., Kusuhara, H., Sugiyama, Y. and Endou,H]
通讯作者:
Y. and Endou,H
共 28 条
Role of endothelial cells and pericyte interdigitation in angiogenesis
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批准号:15580267
-
项目类别:Grant-in-Aid for Scientific Research (C)
-
资助金额:$2.43万
-
财政年份:2003
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负责人:WAKUI Shin
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依托单位:
Endothelial Cell - Pericyte Interdigitation in Angiogenesis
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批准号:12660278
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.56万
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财政年份:2000
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负责人:WAKUI Shin
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依托单位:
Endothelial Cell-Pericyte Interdigitation in Angiogenesis
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批准号:09660332
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.18万
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财政年份:1997
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负责人:WAKUI Shin
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依托单位:
Endothelial Cell-Pericyte Interdigitation is Mediator of Angiogenesis?
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批准号:07806042
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$1.41万
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财政年份:1995
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负责人:WAKUI Shin
-
依托单位:
海外基金