FIBRONECTIN RECEPTOR MEDIATED ADHESION OF P GINGIVALIS
纤连蛋白受体介导的牙龈卟啉单胞菌粘附
基本信息
- 批准号:2131179
- 负责人:
- 金额:$ 2.89万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1992
- 资助国家:美国
- 起止时间:1992-05-01 至 1995-04-30
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Approximately 75% of the adult population suffers from some form of
periodontal disease. Periodontal disease results when virulent gram
negative bacteria colonize the gingival crevice. This colonization
involves specific interactions between bacterial adhesions and epithelial
cell surface receptors. Secreted molecules found in serum, saliva, and
crevicular fluid can also participate in these adhesion events.
Porphyromonas gingivalis is a gram negative obligate anaerobe that is
commonly isolated from periodontal pockets. Its adherence to oral
epithelium is well documented, but the molecular basis for this interaction
is unknown. Fibronectin is known to participate in a number of important
adhesion events involving the integrin family of receptors, and a number of
these receptors have been identified on epithelial cells. In addition,
fibronectin can be expressed in an insoluble form on the surface of
epithelial cells and also secreted by them. Also, soluble fibronectin is
found in both saliva and serum. Finally, several bacterial strains have
been identified which are able to bind various forms of human fibronectin.
Thus the objective of this proposal is to determine the role of fibronectin
in the adhesion of P. gingivalis to oral epithelial cells. Once the role
of fibronectin in bacterial adhesion is determined, preventive therapies
could to be developed which would inhibit this initial colonization event.
Accordingly, the specific aims of this proposal are: (1) to characterize
the interactions between P. gingivalis and fibronectin; (2) to characterize
the fibronectin expression and/or fibronectin binding capacity of oral
epithelium; and (3) to determine the potential role of fibronectin in the
binding of P. gingivalis to oral epithelium.
The ability of P. gingivalis to interact with either soluble and/or
insoluble fibronectin will be determined by means of an ELISA. Both an
epithelial cell line and freshly isolated oral epithelial cells will be
analyzed by flow cytometry to determine the presence of cell surface
fibronectin, receptors for fibronectin, and the ability of the receptors to
bind fibronectin. Adhesion assays will be performed to determine the
binding properties of P. gingivalis and oral epithelium. Importantly, the
ability to use an established cell line as an in vitro model for bacterial
adhesion in the oral cavity will also be investigated.
大约75%的成年人患有某种形式的
牙周病 牙周病毒革时引起
阴性细菌定植在牙龈缝隙中。 这种殖民化
涉及细菌粘连和上皮细胞之间的特定相互作用,
细胞表面受体 在血清,唾液,
裂隙液也可参与这些粘连事件。
牙龈卟啉单胞菌是革兰氏阴性专性厌氧菌,
通常从牙周袋中分离。 其坚持口头
上皮是有据可查的,但这种相互作用的分子基础
不明 已知纤连蛋白参与许多重要的细胞凋亡。
涉及受体的整合素家族的粘附事件,以及许多
这些受体已在上皮细胞上被鉴定。 此外,本发明还提供了一种方法,
纤连蛋白可以以不溶性形式表达在细胞表面,
上皮细胞,也由它们分泌。 此外,可溶性纤连蛋白是
唾液和血清中都有 最后,几种细菌菌株
已经鉴定出能够结合各种形式的人纤连蛋白的人纤连蛋白。
因此,本建议的目的是确定纤维连接蛋白的作用,
牙龈卟啉单胞菌对口腔上皮细胞的粘附。 一旦角色
纤维连接蛋白在细菌粘附中的作用,
能够抑制这种最初的殖民活动。
因此,本提案的具体目标是:(1)确定
牙龈卟啉单胞菌与纤维连接蛋白之间的相互作用;(2)表征
口腔粘膜纤维连接蛋白表达和/或纤维连接蛋白结合能力
上皮细胞;和(3)确定纤维连接蛋白的潜在作用,
牙龈卟啉单胞菌与口腔上皮的结合。
牙龈卟啉单胞菌与可溶性的和/或可溶性的细菌相互作用的能力是显著的。
不溶性纤连蛋白将通过ELISA测定。 两者
上皮细胞系和新鲜分离的口腔上皮细胞将被
通过流式细胞术分析以确定细胞表面
纤连蛋白,纤连蛋白受体,以及受体的能力,
结合纤连蛋白。 将进行粘附试验,以确定
牙龈卟啉单胞菌和口腔上皮的结合特性。 重要的是
使用已建立的细胞系作为细菌体外模型的能力
还将研究口腔中的粘附。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
数据更新时间:{{ journalArticles.updateTime }}
{{
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 }}
KAREN R SNAPP其他文献
KAREN R SNAPP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('KAREN R SNAPP', 18)}}的其他基金
Molecular Basis For Functional Diversity Of PSGL-1
PSGL-1 功能多样性的分子基础
- 批准号:
6890415 - 财政年份:2001
- 资助金额:
$ 2.89万 - 项目类别:
Molecular Basis For Functional Diversity Of PSGL-1
PSGL-1 功能多样性的分子基础
- 批准号:
6636382 - 财政年份:2001
- 资助金额:
$ 2.89万 - 项目类别:
Molecular Basis For Functional Diversity Of PSGL-1
PSGL-1 功能多样性的分子基础
- 批准号:
6752826 - 财政年份:2001
- 资助金额:
$ 2.89万 - 项目类别:
Molecular Basis For Functional Diversity Of PSGL-1
PSGL-1 功能多样性的分子基础
- 批准号:
6332986 - 财政年份:2001
- 资助金额:
$ 2.89万 - 项目类别:
Molecular Basis For Functional Diversity Of PSGL-1
PSGL-1 功能多样性的分子基础
- 批准号:
6520152 - 财政年份:2001
- 资助金额:
$ 2.89万 - 项目类别:
Molecular Basis For Functional Diversity Of PSGL-1
PSGL-1 功能多样性的分子基础
- 批准号:
6665138 - 财政年份:2001
- 资助金额:
$ 2.89万 - 项目类别:
相似海外基金
Development of back bone vectors for chimeric antigen receptors against key molecules, CD47 and CD24, activating macrophages
开发针对关键分子 CD47 和 CD24 的嵌合抗原受体的骨干载体,激活巨噬细胞
- 批准号:
23K06728 - 财政年份:2023
- 资助金额:
$ 2.89万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
CAREER: Engineering next-generation chimeric antigen receptors for cancer immunotherapy using phospho-proteomics
职业:利用磷酸蛋白质组学设计用于癌症免疫治疗的下一代嵌合抗原受体
- 批准号:
2145853 - 财政年份:2022
- 资助金额:
$ 2.89万 - 项目类别:
Continuing Grant
Construction of a drug discovery platform utilizing antigen receptors that regulate the quality of cancer immunity
利用调节癌症免疫质量的抗原受体构建药物发现平台
- 批准号:
22K06603 - 财政年份:2022
- 资助金额:
$ 2.89万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Engineering synthetic adhesion receptors to enhance the sensitivity of therapeutic chimeric antigen receptors
工程合成粘附受体以增强治疗性嵌合抗原受体的敏感性
- 批准号:
MR/W031353/1 - 财政年份:2022
- 资助金额:
$ 2.89万 - 项目类别:
Research Grant
Modeling based design of chimeric antigen receptors for Natural Killer cell-based immunotherapy
用于基于自然杀伤细胞的免疫治疗的嵌合抗原受体的基于建模的设计
- 批准号:
10701754 - 财政年份:2022
- 资助金额:
$ 2.89万 - 项目类别:
Modeling based design of chimeric antigen receptors for Natural Killer cell-based immunotherapy
用于基于自然杀伤细胞的免疫治疗的嵌合抗原受体的基于建模的设计
- 批准号:
10557760 - 财政年份:2022
- 资助金额:
$ 2.89万 - 项目类别:
Chimeric antigen receptors on regulatory T cells as a treatment strategy in auto-immune diseases.
调节性 T 细胞上的嵌合抗原受体作为自身免疫性疾病的治疗策略。
- 批准号:
437200 - 财政年份:2020
- 资助金额:
$ 2.89万 - 项目类别:
Studentship Programs
Molecualr imaging for development of chimeric antigen receptors (CARs) resistant to T cell exhaustion
用于开发抗 T 细胞耗竭的嵌合抗原受体 (CAR) 的分子成像
- 批准号:
20H03536 - 财政年份:2020
- 资助金额:
$ 2.89万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Therapeutic Anti-HIV Chimeric Antigen Receptors Via Stem Cell Delivery
通过干细胞递送治疗性抗 HIV 嵌合抗原受体
- 批准号:
10542442 - 财政年份:2020
- 资助金额:
$ 2.89万 - 项目类别:
Therapeutic Anti-HIV Chimeric Antigen Receptors Via Stem Cell Delivery
通过干细胞递送治疗性抗 HIV 嵌合抗原受体
- 批准号:
10321545 - 财政年份:2020
- 资助金额:
$ 2.89万 - 项目类别: