STRUCTURE AND FUNCTION OF THE ALPHA-E-BETA-7 INTEGRIN
ALPHA-E-BETA-7 整合素的结构和功能
基本信息
- 批准号:2415201
- 负责人:
- 金额:$ 14.09万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1993
- 资助国家:美国
- 起止时间:1993-05-01 至 1998-04-30
- 项目状态:已结题
- 来源:
- 关键词:SDS polyacrylamide gel electrophoresis biological signal transduction cell adhesion cell adhesion molecules electroporation epithelium flow cytometry gene expression human tissue immunoaffinity chromatography immunoprecipitation integrins laboratory mouse laboratory rabbit ligands lymphocyte molecular cloning monoclonal antibody northern blottings nucleic acid hybridization protein structure function receptor binding site directed mutagenesis southern blotting transfection
项目摘要
Recently we identified a novel integrin on human intraepithelial
lymphocytes (IEL) which is composed of a beta7 subunit associated with a
newly identified member of the alpha chain family, here called alphaE.
The alphaEbeta7 complex is expressed on >95% of IEL but on <2% of
peripheral blood lymphocytes. Preliminary evidence suggests that this
alphaEbeta7 integrin is one of the integrins which mediates the adhesion
of intraepithelial lymphocytes to epithelial cells. We propose to study
the structure and function of this alphaEbeta7 integrin and of the
alphaEbeta7 counter-receptor thought to be expressed on epithelial
cells. First, the gene encoding of the alphaE chain will be cloned by
degenerate oligonucleotide screening of an IEL derived lambda-ZAP II
library, and the gene encoding the full length beta7 subunit will be
obtained. Next, the epithelial cell counter-receptor for alphaEbeta7
will be identified by producing anti-epithelial cell monoclonal
antibodies which block the adhesion of IEL and alphaEbeta7 transfectants
to epithelial cells. This epithelial cell adhesion molecule (ECAM-1)
will be characterized biochemically an the gene encoding it will be
cloned by expression of an epithelial cell derived library in COS cells
and selection with the anti-ECAM-1 monoclonal antibody. ECAM-1 will
then be purified and utilized to study the binding of alphaEbeta7 to
this receptor in a defined system, where the ability of alphaEbeta7 to
transduce signals can be assessed. In addition, other potent ligands
for the alphaEbeta7 complex will be identified utilizing monoclonal
antibodies to block the adhesion of IELs to extracellular matrix
proteins. Transfectants expressing either reconstituted alphaEbeta7
heterodimer of ECAM-1 will be generated and utilized to directly confirm
defined alphaEbeta7 functions. Finally, transfectants expressing
mutated alphaE or beta7 subunits will be developed which will be
utilized to evaluate the effect of changes in the structure of the
alphaE or beta7 subunits or the ECAM-1 molecule on the alphaEbeta7
function. In this way we hope to gain information about the role of
this alphaEbeta7 integrin in the development and physiology of
intraepithelial lymphocytes.
最近,我们在人上皮细胞内发现了一种新的整合素,
淋巴细胞(IEL),由β 7亚基组成,
新发现的α链家族成员,这里称为α E。
α Ebeta 7复合物在>95%的IEL上表达,但在<2%的IEL上表达。
外周血淋巴细胞。 初步证据显示,
α E β 7整合素是介导粘附的整合素之一
转化为上皮细胞。 我们建议研究
这种α E β 7整联蛋白的结构和功能,
α Ebeta 7反受体被认为在上皮细胞上表达
细胞 首先,将通过以下方法克隆编码α E链的基因:
IEL衍生的ZAP II的简并寡核苷酸筛选
文库中,并且编码全长β 7亚基的基因将被
得到了 接下来,上皮细胞的α-E β 7反受体
将通过产生抗上皮细胞单克隆抗体
阻断IEL和α E β 7转染子粘附的抗体
上皮细胞。 上皮细胞粘附分子(ECAM-1)
将被生物化学表征,编码它的基因将被
通过在COS细胞中表达上皮细胞来源的文库来克隆
用抗ECAM-1单克隆抗体筛选。 ECAM-1将
然后纯化并用于研究α E β 7与
这种受体在一个确定的系统,其中的能力,
可以评估干扰信号。 此外,其他有效的配体
将利用单克隆抗体
阻断IEL与细胞外基质粘附的抗体
proteins. 表达重组α E β 7
将产生ECAM-1的异二聚体并用于直接确认
alphaEbeta 7功能 最后,表达
突变的α E或β 7亚基将被开发出来,
用于评估结构变化的影响,
α E或β 7亚基或α E β 7上的ECAM-1分子
功能 通过这种方式,我们希望获得有关
这种α-Ebeta 7整合素在发育和生理学中的作用
上皮内淋巴细胞
项目成果
期刊论文数量(2)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Direct and regulated interaction of integrin alphaEbeta7 with E-cadherin.
- DOI:10.1083/jcb.140.1.197
- 发表时间:1998-01-12
- 期刊:
- 影响因子:0
- 作者:Higgins JM;Mandlebrot DA;Shaw SK;Russell GJ;Murphy EA;Chen YT;Nelson WJ;Parker CM;Brenner MB
- 通讯作者:Brenner MB
Lymphocyte adhesion to epithelia and endothelia mediated by the lymphocyte endothelial-epithelial cell adhesion molecule glycoprotein.
淋巴细胞与上皮和内皮的粘附由淋巴细胞内皮-上皮细胞粘附分子糖蛋白介导。
- DOI:
- 发表时间:1999
- 期刊:
- 影响因子:0
- 作者:Shieh,CC;Sadasivan,BK;Russell,GJ;Schon,MP;Parker,CM;Brenner,MB
- 通讯作者:Brenner,MB
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CHRISTINA M PARKER其他文献
CHRISTINA M PARKER的其他文献
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{{ truncateString('CHRISTINA M PARKER', 18)}}的其他基金
Role of Integrin alphaEbeta7 on Th2 Immune Responses
整合素 alphaEbeta7 对 Th2 免疫反应的作用
- 批准号:
6344613 - 财政年份:2000
- 资助金额:
$ 14.09万 - 项目类别:
MUCOSAL IMMUNITY IN INTEGRIN ALPHA E DEFICIENT MICE
整合素 α E 缺陷小鼠的粘膜免疫
- 批准号:
2906082 - 财政年份:1997
- 资助金额:
$ 14.09万 - 项目类别:
Mucosal Immunity in Integrin Alpha-E Deficient Mice
整合素 Alpha-E 缺陷小鼠的粘膜免疫
- 批准号:
6331484 - 财政年份:1997
- 资助金额:
$ 14.09万 - 项目类别:
MUCOSAL IMMUNITY IN INTEGRIN ALPHA E DEFICIENT MICE
整合素 α E 缺陷小鼠的粘膜免疫
- 批准号:
2385106 - 财政年份:1997
- 资助金额:
$ 14.09万 - 项目类别:
MUCOSAL IMMUNITY IN INTEGRIN ALPHA E DEFICIENT MICE
整合素 α E 缺陷小鼠的粘膜免疫
- 批准号:
6339839 - 财政年份:1997
- 资助金额:
$ 14.09万 - 项目类别:
MUCOSAL IMMUNITY IN INTEGRIN ALPHA E DEFICIENT MICE
整合素 α E 缺陷小鼠的粘膜免疫
- 批准号:
2749631 - 财政年份:1997
- 资助金额:
$ 14.09万 - 项目类别:
STRUCTURE AND FUNCTION OF THE ALPHA-E-BETA-7 INTEGRIN
ALPHA-E-BETA-7 整合素的结构和功能
- 批准号:
2186931 - 财政年份:1993
- 资助金额:
$ 14.09万 - 项目类别:
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- 批准号:
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- 资助金额:
$ 14.09万 - 项目类别:
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