Development of New System for Production of Liver Specific Proteins using Cell lines Derived from Human Liver by Radial Flow Type Bioreactor
Development of New System for Production of Liver Specific Proteins using Cell lines Derived from Human Liver by Radial Flow Type Bioreactor
批准号:
10558138
负责人:
NAGAMORI Seishi
金额:
$7.68万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
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
中文摘要
作为肝移植手术的替代方案,许多研究人员一直在朝着功能齐全的人工肝脏的目标努力。近年来,人工肝支持系统被提倡作为等待肝细胞替代治疗或肝移植治疗的患者的临时治疗;所谓的“桥接”治疗。人们认识到,一个有效的人工肝脏系统需要:1)一个有活力和高功能的肝细胞系,2)一个合适的生物反应器环境和外围控制系统,3)一个有效的体外循环系统。然而,传统的系统存在各种缺陷,包括来自非人类细胞的细胞培养物的不兼容性,细胞增殖不足,由于细胞环境不良而导致细胞功能迅速恶化,以及缺乏系统可扩展性。一种新建立的人工肝脏系统克服了许多这些问题,并在定量和定性上证明了长期维持多种肝脏特异性功能的能力,如蛋白质合成、酶活性和药物代谢。
英文摘要
As an alternative to liver transplantation surgery, numerous researchers have been working toward the goal of a fully functional artificial liver. In recent years, artificial liver support systems have been advocated as interim treatments for patients awaiting hepatocyte replacement therapy or liver transplantation treatment ; so-called "bridging" treatments. It is recognized that art effective artificial liver system requires : 1) a viable and highly functional hepatocyte cell line, 2) a suitable bioreactor environment and peripheral control systems, and 3) incorporation within an effective extracorporeal circulatory system. Conventional systems have, however, suffered from various drawbacks including incompatibility of cell cultures deriverd from non-human cells, insufficient cell proliferation, rapid deterioration of cellular function due to an impoverished cellular environment, and lack of system scalability. A newly established artificial liver system overcomes many of these problems and demonstrates a long-term capacity to maintain multiple liver-specific functions, such as protein synthesis, enzyme activity and drug metablism, both quantitatively and qualitatively.
期刊论文(30)
专著(0)
科研奖励(0)
会议论文
登录
查看更多内容
永森静志 他: "KEY WORD 2000〜2001 肝胆膵"先端医学社. 261 (1999)
Shizushi Nagamori 等人:“关键词 2000-2001 肝胆胰”Senshin Igakusha 261 (1999)。
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
M.Kawada,S.Nagamori,H.Aizaki,K.Fukaya,M.Niiy,T.Matsuura,H.Sujino,S.Hasumura,H.Yoshida,S.Mizutani,and H.Ikenaqga.: "Massive Culture of Human Liver Cancer Cells in a Newly Developed Radial Flow Bioreactor System : Ultrafine Structure of Functionally Enhance
M.Kawada、S.Nagamor、H.Aizaki、K.Fukaya、M.Niiy、T.Matsuura、H.Sujino、S.Hasumura、H.Yoshida、S.Mizutani 和 H.Ikenaqga:“大规模文化
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
H.Aizaki,Y.Aoki,T.Harada,K.Ishii,T.Suzuki,S.Nagamori,G.Toda,Y.Matsuura and T.Miyamura: "Full-length Complementary DNA of Hepatitis C Virus Genome from an Infectious Blood Sample"Hepatology. 27(2). 621-627 (1998)
H.Aizaki、Y.Aoki、T.Harada、K.Ishii、T.Suzuki、S.Nagamori、G.Toda、Y.Matsuura 和 T.Miyamura:“来自传染性丙型肝炎病毒基因组的全长互补 DNA
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
永森 静志: "特集に寄せて(特集:人工肝臓への道-肝細胞とバイオリアクターの進歩)" 組織培養学. 23. 280-283 (1997)
Shizushi Nagamori:“特刊(专题:人工肝之路 - 肝细胞和生物反应器的进展)”组织培养科学。23. 280-283 (1997)
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
Nakada J, Kawada M, Matsuura T, Nagamori S, et al.: "Effects of nerre growth factor and glucocorticoid on cultured human pheochromocytoma cells"Med. Electron Microsc.. 31. 24-30 (1998)
Nakada J,Kawada M,Matsuura T,Nagamori S,等:“神经生长因子和糖皮质激素对培养的人嗜铬细胞瘤细胞的影响”Med。
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
共 29 条
Studies on proliferating mechanism of hepatitis C virus using cultured human liver cell lines by radialflowtype-bioreactor
-
批准号:09480257
-
项目类别:Grant-in-Aid for Scientific Research (B)
-
资助金额:$7.94万
-
财政年份:1997
-
负责人:NAGAMORI Seishi
-
依托单位:
A New Liver Support System Using a Radial Flow Bioreactor
-
批准号:07458238
-
项目类别:Grant-in-Aid for Scientific Research (B)
-
资助金额:$4.61万
-
财政年份:1995
-
负责人:NAGAMORI Seishi
-
依托单位:
Studies on the separation and mechanism of albumin synthesis in albumin-positive cells derived from Nagase analbuminemic rats (NAR).
-
批准号:63570332
-
项目类别:Grant-in-Aid for General Scientific Research (C)
-
资助金额:$1.09万
-
财政年份:1988
-
负责人:NAGAMORI Seishi
-
依托单位:
海外基金