MECHANISMS OF BILE PIGMENT EXCRETION
胆色素排泄机制
基本信息
- 批准号:6651940
- 负责人:
- 金额:$ 63.7万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1984
- 资助国家:美国
- 起止时间:1984-12-01 至 2005-09-30
- 项目状态:已结题
- 来源:
- 关键词:Native Americans bile pigments biological transport cholanate compound cholestasis confocal scanning microscopy fluorescent dye /probe fungal genetics gene mutation genetic disorder human genetic material tag human subject laboratory rat lipid transport liver metabolism membrane transport proteins messenger RNA molecular cloning phosphatidylinositol 3 kinase phospholipids polymerase chain reaction protein sequence protein structure function transfection yeasts
项目摘要
Using molecular, cell biologic, biochemical and immunomorphologic methods,
we request to continue long range studies of mechanisms involved in the
transfer of various organic molecules (i.e., bile acids, pigments, drugs,
metabolites and others) from blood to bile and back.
In particular, we seek to determine the structure, function and regulation
of four bile canalicular transporters and, ultimately, their dysfunction
in developmental, acquired and inheritable cholestasis:
(a) Cloning, sequencing and purification of the ATP-dependent transporters
for bile acids and nonbile acid organic anions in mutant budding and
fisson yeast in order to generate probes for identifying and studying
structure and regulation of the mammalian homologues (which, due to low
abundance, have frustrated efforts at purification and cloning).
(b) Preliminary evidence suggests that mdr2, the major multidrug
resistance gene product in the canaliculus, has ATP-dependent phospholipid
translocase activity and increases phospholipid release from cell plasma
membranes. Therefore, we seek to determine how these processes are
related with respect to canalicular phospholipid transport, and the
possible role of mdr2 in the "vanishing bile duct syndrome".
(c) Cloning, sequencing and study of the regulation of the canalicular Na+
dependent purine transporter which conserves nucleosides in hepatocytes.
采用分子、细胞生物学、生物化学和免疫形态学方法,
我们要求继续长期研究参与
各种有机分子的转移(即,胆汁酸,色素,药物,
代谢物和其他)从血液到胆汁并返回。
特别是,我们寻求确定结构,功能和监管
四种胆小管转运蛋白的功能障碍,
在发育性、获得性和遗传性胆汁淤积中:
(a)ATP依赖转运蛋白的克隆、测序和纯化
胆汁酸和非胆汁酸有机阴离子在突变体出芽和
fisson酵母,以产生用于鉴定和研究的探针
哺乳动物同源物的结构和调节(由于低
丰富,使纯化和克隆的努力受挫)。
(b)初步证据表明,主要的多药耐药基因mdr 2
抗性基因产物存在于小管中,具有ATP依赖性磷脂
移位酶活性和增加磷脂从细胞血浆中释放
膜。 因此,我们试图确定这些过程是如何
与小管磷脂转运有关,
mdr 2在“胆管消失综合征”中的作用
(c)小管Na ~+的克隆、测序及调控研究
在肝细胞中保存核苷的依赖性嘌呤转运蛋白。
项目成果
期刊论文数量(54)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Regulation of growth and differentiation of a rat hepatoma cell line by the synergistic interactions of hormones and collagenous substrata.
通过激素和胶原基质的协同相互作用调节大鼠肝癌细胞系的生长和分化。
- DOI:10.1083/jcb.97.4.1179
- 发表时间:1983
- 期刊:
- 影响因子:0
- 作者:Gatmaitan,Z;Jefferson,DM;Ruiz-Opazo,N;Biempica,L;Arias,IM;Dudas,G;Leinwand,LA;Reid,LM
- 通讯作者:Reid,LM
Biliary transport of glutathione S-conjugate by rat liver canalicular membrane vesicles.
大鼠肝小管膜囊泡对谷胱甘肽 S-结合物的胆汁转运。
- DOI:
- 发表时间:1984
- 期刊:
- 影响因子:0
- 作者:Inoue,M;Akerboom,TP;Sies,H;Kinne,R;Thao,T;Arias,IM
- 通讯作者:Arias,IM
The effect of limited proteolysis on enzymatic, binding and immunological properties of ligandin.
有限蛋白水解对配体蛋白的酶促、结合和免疫学特性的影响。
- DOI:10.1016/0006-291x(82)90670-2
- 发表时间:1982
- 期刊:
- 影响因子:3.1
- 作者:Bhargava,MM;Ohmi,N;Arias,IM
- 通讯作者:Arias,IM
The sinusoidal domain of the plasma membrane of rat hepatocytes contains an amiloride-sensitive Na+/H+ antiport.
大鼠肝细胞质膜的正弦结构域含有阿米洛利敏感的 Na /H 反向转运。
- DOI:
- 发表时间:1984
- 期刊:
- 影响因子:0
- 作者:Arias,IM;Forgac,M
- 通讯作者:Forgac,M
The mechanism of biliary secretion of reduced glutathione. Analysis of transport process in isolated rat-liver canalicular membrane vesicles.
胆汁分泌还原型谷胱甘肽的机制。
- DOI:10.1111/j.1432-1033.1983.tb07590.x
- 发表时间:1983
- 期刊:
- 影响因子:0
- 作者:Inoue,M;Kinne,R;Tran,T;Arias,IM
- 通讯作者:Arias,IM
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
IRWIN Monroe ARIAS其他文献
IRWIN Monroe ARIAS的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('IRWIN Monroe ARIAS', 18)}}的其他基金
PI KINASES, CANALICULAR TRANSPORTERS AND CHOLESTASIS
PI 激酶、小管转运蛋白和胆汁淤积
- 批准号:
6177912 - 财政年份:1999
- 资助金额:
$ 63.7万 - 项目类别:
PI KINASES, CANALICULAR TRANSPORTERS AND CHOLESTASIS
PI 激酶、小管转运蛋白和胆汁淤积
- 批准号:
2910977 - 财政年份:1999
- 资助金额:
$ 63.7万 - 项目类别:
PI KINASES, CANALICULAR TRANSPORTERS AND CHOLESTASIS
PI 激酶、小管转运蛋白和胆汁淤积
- 批准号:
6523750 - 财政年份:1999
- 资助金额:
$ 63.7万 - 项目类别:
PI KINASES, CANALICULAR TRANSPORTERS AND CHOLESTASIS
PI 激酶、小管转运蛋白和胆汁淤积
- 批准号:
6650341 - 财政年份:1999
- 资助金额:
$ 63.7万 - 项目类别:
PI KINASES, CANALICULAR TRANSPORTERS AND CHOLESTASIS
PI 激酶、小管转运蛋白和胆汁淤积
- 批准号:
6381368 - 财政年份:1999
- 资助金额:
$ 63.7万 - 项目类别:
相似海外基金
Structural Studies of Algal Bile Pigments and Proteins
藻胆色素和蛋白质的结构研究
- 批准号:
8314386 - 财政年份:1984
- 资助金额:
$ 63.7万 - 项目类别:
Standard Grant














{{item.name}}会员




