ION TRANSPORT IN COLLECTING CELL CULTURES
ION TRANSPORT IN COLLECTING CELL CULTURES
批准号:
2140623
负责人:
ELSA N. BELLO-REUSS
金额:
$17.78万
依托单位国家:
美国
项目类别:
财政年份:
1986
资助国家:
美国
项目状态:
已结题
起止时间:
1986-08-01 至 1994-11-30
关键词:
aldosterone basolateral membrane cell type dopamine electrophysiology epithelium hormone regulation /control mechanism ion transport kidney cell laboratory rabbit membrane permeability membrane potentials microelectrodes mixed tissue /cell culture neurotransmitters norepinephrine potassium renal tubule acidosis
中文摘要
我们的目标是了解离子的输运性质和它的机制。
皮质集合管不同细胞类型的调控
(电荷耦合器件)。具体目标是:1.继续描述离子传输
在培养的细胞中表达的机制。混合的ccd培养将是
用于确定离子传输机制,以及ADH的影响,
醛固酮和异丙肾上腺素在不同的转运体上。2.学习
细胞内外pH对细胞生物学及转运的影响
CCD单分子膜的功能。2.1.以评估在
不同细胞类型的比例和细胞形态的变化
对培养物酸碱状态变化的反应。2.2.至
建立位于根尖和根尖的转运蛋白的pH依赖关系
不同细胞的基侧膜。我们将研究
三种细胞类型的导电和非导电离子转运途径
在基础条件下及其对急性和慢性变化的反应
底侧和/或根尖溶液的pH值。3.为了刻画,
结构和功能上均一的主细胞单层
和嵌插细胞。3.1.主要的超微结构和功能。
我们将研究细胞单层:我们将在细胞膜上进行表征
提高基线离子传输机制的水平及其调节
激素(ADH、醛固酮、异丙肾上腺素)。3.2.的同质培养
插入的细胞,最初被鉴定为α或β细胞,
将在有和没有激素刺激的情况下进行研究。特价
将考虑细胞转化的可能性
键入到另一个。单层的CCD细胞将使我们能够收集基本的
细胞膜和单膜离子传输机制的研究进展
级别。它们也应该是生物化学和分子生物学的有用工具
学习。同质培养将允许定量研究,而不需要
不同类型相邻细胞的混杂影响。这些
研究有助于我们理解肾小管的发病机制。
离子转运缺陷,如肾小管性酸中毒、浓度
缺陷和K+分泌异常。
英文摘要
We aim to understand the ion transport properties and the mechanisms of its
regulation in the different cell types of the cortical collecting duct
(CCD). Specific aims are: 1. Continue characterizing the ion-transport
mechanisms expressed in CCD cells in culture. Mixed CCD cultures will be
used to identify mechanisms of ion transport, and the effects of ADH,
aldosterone, and isoproterenol on the different transporters. 2. To study
the effects of intra and extracellular pH on the cell biology and transport
functions of CCD monolayers. 2.1. To assess the modifications in the
proportion of the different cell types and the morphological changes in
response to alterations in acid-base status of the cultures. 2.2. To
establish the pH dependence of the transporters located in the apical and
basolateral membranes of the different cells. We will examine the
conductive and nonconductive ion-transport pathways of the three cell types
under basal conditions and their responses to acute and chronic changes in
pH of basolateral and/or apical solutions. 3. To characterize,
structurally and functionally, homogeneous monolayers of principal cells
and intercalated cells. 3.1. The ultrastructure and function of principal-
cell monolayers will be studied: We will characterize at the cell-membrane
level the baseline ion transport mechanisms and their regulation by
hormones (ADH, aldosterone, isoproterenol). 3.2. Homogeneous cultures of
intercalated cells, initially identified as either alpha or beta cells,
will be studied with and without hormonal stimulation. Special
consideration will be given to the possibility of transformation of a cell
type to another. Monolayers of CCD cells will allow us to gather basic
information on ion transport mechanisms at the cellular and single-membrane
levels. They should also be useful tools for biochemical and molecular
studies. Homogenous cultures will permit quantitative studies without the
confounding influences of neighboring cells of different type. These
studies could help our understanding of the pathogenesis of renal tubule
ion-transport defects, such as renal tubular acidosis, concentration
defects and K+ secretion abnormalities.
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Characterization of acid-base transport mechanisms in the kidney cell line RCCT-28A.
肾细胞系 RCCT-28A 中酸碱转运机制的表征。
DOI:
10.1038/ki.1993.29
发表时间:
1993
期刊:
Kidney international
影响因子:
19.6
作者:
[Bello-Reuss,E]
通讯作者:
Bello-Reuss,E
Xenobiotic transport differences in mouse mesangial cell clones expressing mdr1 and mdr3.
表达 mdr1 和 mdr3 的小鼠系膜细胞克隆中的异生素转运差异。
DOI:
10.1152/ajpcell.1996.270.3.c910
发表时间:
1996
期刊:
The American journal of physiology
影响因子:
--
作者:
[Ernest,S, Bello-Reuss,E]
通讯作者:
Bello-Reuss,E
Electrophysiological studies on primary cultures of proximal tubule cells.
近曲小管细胞原代培养物的电生理学研究。
DOI:
10.1152/ajprenal.1986.251.3.f490
发表时间:
1986
期刊:
The American journal of physiology
影响因子:
--
作者:
[Bello-Reuss,E, Weber,MR]
通讯作者:
Weber,MR
Characterization of peanut-lectin (+) cells derived from the RCCT-28A cell line.
源自 RCCT-28A 细胞系的花生凝集素 ( ) 细胞的表征。
DOI:
10.1038/ki.1993.30
发表时间:
1993
期刊:
Kidney international
影响因子:
19.6
作者:
[Bello-Reuss,E]
通讯作者:
Bello-Reuss,E
Electrophysiological studies of primary cultures of rabbit distal tubule cells.
兔远端肾小管细胞原代培养物的电生理学研究。
DOI:
10.1152/ajprenal.1987.252.5.f899
发表时间:
1987
期刊:
The American journal of physiology
影响因子:
--
作者:
[Bello-Reuss,E, Weber,MR]
通讯作者:
Weber,MR
共 6 条
FUNCTION OF P-GLYCOPROTEIN IN KIDNEY CELLS
-
批准号:2838143
-
项目类别:
-
资助金额:$24.86万
-
财政年份:1996
-
负责人:ELSA N. BELLO-REUSS
-
依托单位:
FUNCTION OF P-GLYCOPROTEIN IN KIDNEY CELLS
-
批准号:2016822
-
项目类别:
-
资助金额:$24.19万
-
财政年份:1996
-
负责人:ELSA N. BELLO-REUSS
-
依托单位:
FUNCTION OF P-GLYCOPROTEIN IN KIDNEY CELLS
-
批准号:2608460
-
项目类别:
-
资助金额:$24.25万
-
财政年份:1996
-
负责人:ELSA N. BELLO-REUSS
-
依托单位:
ION TRANSPORT & ITS REGULATION IN PROXIMAL RENAL TUBULES
-
批准号:3238162
-
项目类别:
-
资助金额:$9.53万
-
财政年份:1986
-
负责人:ELSA N. BELLO-REUSS
-
依托单位:
ION TRANSPORT IN COLLECTING CELL CULTURES
-
批准号:3238160
-
项目类别:
-
资助金额:$15.12万
-
财政年份:1986
-
负责人:ELSA N. BELLO-REUSS
-
依托单位:
ION TRANSPORT IN COLLECTING CELL CULTURES
-
批准号:3238163
-
项目类别:
-
资助金额:$15.53万
-
财政年份:1986
-
负责人:ELSA N. BELLO-REUSS
-
依托单位:
ION TRANSPORT IN COLLECTING CELL CULTURES
-
批准号:3238165
-
项目类别:
-
资助金额:$16.89万
-
财政年份:1986
-
负责人:ELSA N. BELLO-REUSS
-
依托单位:
ION TRANSPORT IN COLLECTING CELL CULTURES
-
批准号:3238164
-
项目类别:
-
资助金额:$15.84万
-
财政年份:1986
-
负责人:ELSA N. BELLO-REUSS
-
依托单位:
ION TRANSPORT & ITS REGULATION IN PROXIMAL RENAL TUBULES
-
批准号:3238166
-
项目类别:
-
资助金额:$3.74万
-
财政年份:1986
-
负责人:ELSA N. BELLO-REUSS
-
依托单位:
ION TRANSPORT & ITS REGULATION IN PROXIMAL RENAL TUBULES
-
批准号:3238161
-
项目类别:
-
资助金额:$9.38万
-
财政年份:1986
-
负责人:ELSA N. BELLO-REUSS
-
依托单位:
ION TRANSPORT & ITS REGULATION IN PROXIMAL RENAL TUBULES
-
批准号:3231751
-
项目类别:
-
资助金额:$5.38万
-
财政年份:1983
-
负责人:ELSA N. BELLO-REUSS
-
依托单位:
ION TRANSPORT & ITS REGULATION IN PROXIMAL RENAL TUBULES
-
批准号:3152793
-
项目类别:
-
资助金额:$8.95万
-
财政年份:1983
-
负责人:ELSA N. BELLO-REUSS
-
依托单位:
海外基金