课题基金 / 基金详情

Development of humanized-liver mice using hepatocyte derived from isolated liver tissue from recipient or donor of living donor liver transplantation

Development of humanized-liver mice using hepatocyte derived from isolated liver tissue from recipient or donor of living donor liver transplantation
使用来自活体肝移植受者或供者的分离肝组织的肝细胞开发人源化肝小鼠
批准号:
23300162
负责人:
TANOUE Akito
金额:
$5.82万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
2011
资助国家:
日本
项目状态:
已结题
起止时间:
2011-11-18 至 2014-03-31

项目摘要

项目成果

TANOUE Akito的其他基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
In this study, we tried for development of humanized-liver mice in which the liver is reconstitute with human hepatocyte derived from isolated liver tissue from recipient or donor of living donor liver transplantation. We demonstrated that, in identical hepatocyte derived from one recipient, freshly (non-freezing) hepatocytes were most effective engrafted in mouse liver compared with hepatocytes refrigerated at a temperature of 4 degrees overnight or freeze-stocked hepatocytes. On the other hand, there is no correlation between cell viability at isolation of hepatocyte and human albumin level in humanized-liver mice. These results indicated that freshly hepatocyte is useful for development of humanized-liver mice, and improvement of freezing method for hepatocyte may lead to effective development of humanized-liver mice.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
HEPATOCYTES TRANSPLANTATION FOR AN INFANT OF ORNITHINE TRANSCARBAMYLASE DEFICIENCY USING CELLS ISOLATED FROM LIVING DONOR REDUCED-GRAFT TISSUE
使用从活体供体减数移植物组织中分离的细胞对鸟氨酸转氨酶缺乏症婴儿进行肝细胞移植
DOI: --
发表时间: 2014
期刊:
影响因子: --
作者: [Matsui A, Horikawa R, Yamamoto A, Sakamoto S, Shigeta T, Nosaka S, Fujimoto J, Tanoue A, Nakamura K, Umezawa A, Matsubara Y, Kasahara M.]
通讯作者: Kasahara M.
胆道閉鎖症の病因に関する最近の知見-特に発生異常説に関して-
关于胆道闭锁发病机制的最新发现 - 特别是关于异常发育理论 -
DOI: --
发表时间: 2011
期刊: Organ Biology
影响因子: --
作者: [中村和昭, 田上昭人]
通讯作者: 田上昭人
Development of humanized-liver mice using hepatocyte derived from pediatric liver/biliary tract diseases and investigation of pathological mechanism of liver/biliary tract diseases.
Analysis of urogenital function with mutant mice lacking for single or multiple alpha 1 adrenergic receptor.
Analysis of cardiovascular function with mutant mice lacking for single or multiple alpha 1 adrenergic receptor.
In vitro analysis of signaling pathway involved in pathgenesis of renal or cardiac disease using animal models.