Mechanism of Recognition of Cells Denatured by Oxidative Stress
氧化应激变性细胞的识别机制
基本信息
- 批准号:07672390
- 负责人:
- 金额:$ 1.6万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Scientific Research (C)
- 财政年份:1995
- 资助国家:日本
- 起止时间:1995 至 1996
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Based on our previous findings that oxidatively damaged erythrocytes are recognized by anti-band 3 glycoprotein autoantibodies and macrophages, we have elucidated the mechanism of recognition of the oxidized erythrocytes, and examined response of macrophages against aged and apoptotic cells.I MECHANISM OF RECOGNITION OF OXIDIZED CELLS1) Ligands on oxidized erythrocytes for anti-band 3 autoantibodies were found to be clusters of poly-N-acetyllactosaminyl saccharide chains of band 3 formed by band 3 aggregation by oxidative mechanism.2) The clusters of the band 3 saccharide chains were also found to be the recognition determinants for macrophages.3) Multiple species of macrophage membrane proteins having poly-N-acetyllact osamine-binding ability were characterized as receptors for the oxidized erythrocytes. One of these proteins, with a molecular weight of 50kD,was purified and its N-terminal 10 amino acid sequence was elucidated. Result of homology search indicated that the 50kDa protein is a new protein.II MECHANISM OF RECOGNITION OF AGED CELLSNeutrophils incubated in vitro, a model of aged somatic cells, were found to be recognized by macrophages.III MECHANISM OF RECOGNITION OF APOPTOTIC CELLSInduction of apoptosis in cultured cells by some agents resulted in recognition by macrophages, although determinants on the apoptotic cells recognized by macrophages are unknown.
基于我们之前的发现,氧化损伤红细胞被抗3带糖蛋白自身抗体和巨噬细胞识别,我们阐明了氧化红细胞的识别机制,并研究了巨噬细胞对衰老和凋亡细胞的反应。1氧化细胞的识别机制1)氧化红细胞上抗3带自身抗体的配体是由氧化机制形成的3带聚集形成的聚n -乙酰乳胺基糖链簇。2) 3带糖链簇也被发现是巨噬细胞识别的决定因素。3)多种巨噬细胞膜蛋白具有聚n -乙酰乳糖氨基结合能力,可作为氧化红细胞的受体。纯化了其中一个分子量为50kD的蛋白,并对其n端10个氨基酸序列进行了分析。同源性分析表明,50kDa蛋白为新蛋白。体外培养的中性粒细胞作为衰老体细胞的模型,可以被巨噬细胞识别。虽然巨噬细胞识别凋亡细胞的决定因素尚不清楚,但某些药物诱导培养细胞凋亡可导致巨噬细胞识别。
项目成果
期刊论文数量(15)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Masatoshi Beppu: "Poly-N-acetyllactosaminyl Saccharide Chains of Band 3 as Determinants for Anti-band 3 Autoantibody Binding to Senescent--" Cell.Mol.Biol.42. 1007-1024 (1996)
Masatoshi Beppu:“带 3 的聚 N-乙酰基乳糖胺基糖链作为抗带 3 自身抗体与衰老结合的决定因素 -”Cell.Mol.Biol.42。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Masatoshi Beppu: "Poly-N-acetyllactosaminyl:Saccharide Chains of Band 3 as determi-nants for Anti-band 3 Autoantibody Binding to Senescent and---" Cell.Mol.Biol.42(7). 1007-1024 (1996)
Masatoshi Beppu:“聚-N-乙酰基乳糖胺基:带 3 的糖链作为抗带 3 自身抗体与衰老结合的决定因素以及——”Cell.Mol.Biol.42(7)。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Masatoshi Beppu: "Recognition of Poly-N-acetyllactosaminyl Saccharide Chains on Iron-Oxidized Erythrocytes by Human Monocytic Leukemia Cell---" Biol.Pharm.Bull.19. 188-194 (1996)
Masatoshi Beppu:“人单核细胞白血病细胞对铁氧化红细胞上聚-N-乙酰基乳糖胺基糖链的识别---”Biol.Pharm.Bull.19。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Shigetoshi Eda: "Characterization of Lactoferrin-Binding Proteins of Human Macrophage Membrane : Multiple Species of Lactoferrin-Binding-" Biol.Pharm.Bull.20. 127-133 (1997)
Shigetoshi Eda:“人巨噬细胞膜乳铁蛋白结合蛋白的表征:乳铁蛋白结合的多种种类”Biol.Pharm.Bull.20。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Shigetoshi Eda et al.: "Characterization of lactoferrin-binding proteins of human macrophage membrane : Multiple species of lactoferrin-binding proteins with polylactosamine-binding ability." Biol.Pharm.Bull.20. 127-133 (1997)
Shigetoshi Eda 等人:“人巨噬细胞膜乳铁蛋白结合蛋白的表征:具有聚乳糖胺结合能力的多种乳铁蛋白结合蛋白。”
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
{{
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 }}
BEPPU Masatoshi其他文献
BEPPU Masatoshi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('BEPPU Masatoshi', 18)}}的其他基金
STUDY ON THE FUNCTIONS OF CELL-SURFACE SHUTTLE PROTEIN NUCLEOLIN
细胞表面穿梭蛋白核仁蛋白的功能研究
- 批准号:
19590080 - 财政年份:2007
- 资助金额:
$ 1.6万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Molecular mechanisms of the carbohydrate-dependent recognition and clearance of apoptotic cells and oxidized cells by macrophages.
巨噬细胞对凋亡细胞和氧化细胞的碳水化合物依赖性识别和清除的分子机制。
- 批准号:
13470492 - 财政年份:2001
- 资助金额:
$ 1.6万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Structure and function of a lectin-like protein of macrophage cell membrane that recognizes oxidized cells
识别氧化细胞的巨噬细胞膜凝集素样蛋白的结构和功能
- 批准号:
11672187 - 财政年份:1999
- 资助金额:
$ 1.6万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Structural and Functional Studies of a Protease That Preferentially Degrades Oxidized Proteins
优先降解氧化蛋白的蛋白酶的结构和功能研究
- 批准号:
09672256 - 财政年份:1997
- 资助金额:
$ 1.6万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
相似海外基金
Host Defense Small Molecule Development for COVID-19 Treatment by Targeting Lysosome
通过靶向溶酶体治疗 COVID-19 的宿主防御小分子开发
- 批准号:
10735492 - 财政年份:2023
- 资助金额:
$ 1.6万 - 项目类别:
Regulation of the pathological condition of sepsis by focusing the senolytic activity of host defense peptide LL-37
通过集中宿主防御肽 LL-37 的衰老活性来调节脓毒症的病理状况
- 批准号:
23K06549 - 财政年份:2023
- 资助金额:
$ 1.6万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
A new interpretation of contact activation system: A host defense mechanism for hemostasis and infection control
接触激活系统的新解释:止血和感染控制的宿主防御机制
- 批准号:
23H02383 - 财政年份:2023
- 资助金额:
$ 1.6万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Commensal bacterial metabolism of dietary phytate in host defense
膳食植酸盐在宿主防御中的共生细菌代谢
- 批准号:
10738360 - 财政年份:2023
- 资助金额:
$ 1.6万 - 项目类别:
Th17 extracellular trap-mediated antimicrobial host defense in acne vulgaris
寻常痤疮中 Th17 细胞外陷阱介导的抗菌宿主防御
- 批准号:
10502200 - 财政年份:2022
- 资助金额:
$ 1.6万 - 项目类别:
Follistatin-like 1 Mediated Host Defense in Bacterial Pneumonia
类卵泡抑素 1 介导细菌性肺炎中的宿主防御
- 批准号:
10636904 - 财政年份:2022
- 资助金额:
$ 1.6万 - 项目类别:
Intestinal O-GlcNAc signaling and mucosal host defense
肠道 O-GlcNAc 信号传导和粘膜宿主防御
- 批准号:
10444727 - 财政年份:2022
- 资助金额:
$ 1.6万 - 项目类别:
Function of host defense peptides in pathophysiology of intestinal diseases in production animals
宿主防御肽在生产动物肠道疾病病理生理学中的作用
- 批准号:
RGPIN-2017-04832 - 财政年份:2022
- 资助金额:
$ 1.6万 - 项目类别:
Discovery Grants Program - Individual
Novel Antimicrobial Host Defense Peptides: Design and Immunomodulatory Function
新型抗菌宿主防御肽:设计和免疫调节功能
- 批准号:
RGPIN-2022-03089 - 财政年份:2022
- 资助金额:
$ 1.6万 - 项目类别:
Discovery Grants Program - Individual














{{item.name}}会员




