by using DNA microarray
通过使用DNA微阵列
基本信息
- 批准号:13470395
- 负责人:
- 金额:$ 9.86万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Scientific Research (B)
- 财政年份:2001
- 资助国家:日本
- 起止时间:2001 至 2003
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
The periodontium functions as a single unit, even though each of its components has a distinct function, composition and connective tissue architecture. Thus it is important and significant to know molecular functions of each periodontal tissue cells using the genome-based research technology. In this study, we constructed the cell culture system depend on each periodontal tissue cell type, gingival epithelial, gingival fibroblastic, periodontal ligament derived, and osteoblatic cells, concerning to specific process of periodontal diseases, and analyzed a large scale of gene expression monitoring using bioinformatics technology. (1) Human gingival epithelial. cells and gingival fibroblasts were primary cultured from human normal gingival tissue, and a DNA microarray technique was used to analyze the different gene expressions. (2) Periodontal ligament derived cells were challenged with mechanical stress, periodontal pathogen LPS and Emdogain, and monitored those gene expression changes … More . (3) Osteoblasts were irradiated with low level diode laser and constructed subtractive gene library and analyzed genes enhanced transcription level, and further analyzed using DNA microarray technology. (4) Human mesenchymal bone marrow stem cells were induced to osteoblasts and monitored gene expression levels using GeneChip. (5) Human placenta trophoblasts were challenged by caffeine, and monitored gene expression levels using DNA inicroarray, further, rat placenta from caffeine feeding pregnant mouse were analyzed by RT-PCR. Effect of ageing on gene expression leve in submandibular glands of mouse was examined by DNA microarray. The reasons why we conducted these study were : periodontal diseases induced low birth infant; saliva components strongly supports health of periodontal tissues.A large scale of gene expression profiling conducted by our experimental models in each periodontal tissues cells, may let us to well understand the specific pathological process of periodontal diseases, to develop new approach of prevention of this disease, and to help the regeneration of periodontal tissues. Less
牙周化的单位,即使是艰难的组成部分,都有尤其是知道的,并且知道分子funcheodyther tistruection该系统依赖于牙周组织类型,牙龈上皮,牙周培养物和骨细胞细胞,涉及牙周疾病的特定过程,并分析了大规模的基因表达监测生物信息信息技术(1)人类牙龈上皮分析不同的基因LPS和EMDOGAIN,并监测了用Lowlaser Laser激光辐射的成骨细胞变化使用GENECHIP进行茎到成骨细胞,并使用DNA不阵列监测基因表达水平,此外,通过测试了咖啡因喂养孕妇的RT-PCR胎盘的大鼠胎盘,并通过亚细质腺体的基因表达效果检查DNA微阵列。牙周组织。
项目成果
期刊论文数量(64)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Hamajima S et al.: "Effect of low-level laser irradiation on osteoglycin gene expression in osteoblasts"Lasers in Medical Science. 18・2. 78-82 (2003)
Hamajima S 等:“低强度激光照射对成骨细胞中骨甘氨酸基因表达的影响”Lasers in Medical Science 18・2 (2003)。
- DOI:
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- 影响因子:0
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早川光央 他: "ハツカネズミ顎下腺成長因子の加齢による遺伝子発現変動のDNAマイクロアレイ解析"醫學と生物學. 145. 93-96 (2002)
Mitsuo Hayakawa 等人:“小鼠颌下腺生长因子基因表达的年龄相关变化的 DNA 微阵列分析”医学与生物学,145. 93-96 (2002)。
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Tanuma A et al.: "Caffeine enhances the expression of the angiotensin II type 2 receptor mRNA in BeWo cell culture and in the rat placenta."Placenta. 24. 638-647 (2003)
Tanuma A 等人:“咖啡因增强 BeWo 细胞培养物和大鼠胎盘中血管紧张素 II 2 型受体 mRNA 的表达。”胎盘。
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- 影响因子:0
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Abiko Y.: "Inhibition of inflammation"The Qintessence. 22. 186-190 (2003)
Abiko Y.:“抑制炎症”的琴精。
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- 影响因子:0
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Nomura K et al.: "Caffeine suppresses the expression of the Bcl-2 mRNA in BeWo cell culture and rat placenta."J.Nut.Biochem.. 15. 342-349 (2004)
Nomura K 等人:“咖啡因抑制 BeWo 细胞培养物和大鼠胎盘中 Bcl-2 mRNA 的表达。”J.Nut.Biochem.. 15. 342-349 (2004)
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ABIKO Yoshimitsu其他文献
ABIKO Yoshimitsu的其他文献
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{{ truncateString('ABIKO Yoshimitsu', 18)}}的其他基金
Searching newly targets and applying their antibodies for the periodontal disease, furthermore development of IT drugs.
寻找牙周病的新靶点并应用其抗体,进一步开发IT药物。
- 批准号:
21390497 - 财政年份:2009
- 资助金额:
$ 9.86万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Integrate research of genomics and proteomics of novel molecular targets for development of periodontal diseases cure
整合基因组学和蛋白质组学新分子靶点研究,开发牙周病治疗方法
- 批准号:
16209063 - 财政年份:2004
- 资助金额:
$ 9.86万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
Construction of human monoclonal antibodies for passive immuno therapy of oral diseases using Xenomouse
利用 Xenomouse 构建用于口腔疾病被动免疫治疗的人单克隆抗体
- 批准号:
13357017 - 财政年份:2001
- 资助金额:
$ 9.86万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
A construction of cDNA library and categorization of genes by subtraction in prokaryote - A gene cloning of new known gene associated with pathogenic factors in P. gingivalis-
原核生物cDNA文库构建及基因消减分类-牙龈卟啉单胞菌致病因子相关新已知基因的基因克隆-
- 批准号:
09470405 - 财政年份:1997
- 资助金额:
$ 9.86万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Development of peptide component vaccine against P.gingivalis
牙龈卟啉单胞菌肽成分疫苗的研制
- 批准号:
06671871 - 财政年份:1994
- 资助金额:
$ 9.86万 - 项目类别:
Grant-in-Aid for General Scientific Research (C)
Identification of periodontal pathogen by DNA probe-biolobiclal and chemical luminescence system
DNA探针-生物化学发光系统鉴定牙周病原菌
- 批准号:
05557086 - 财政年份:1993
- 资助金额:
$ 9.86万 - 项目类别:
Grant-in-Aid for Developmental Scientific Research (B)
Gene Cloning of Glucosyltransferase Synthesizing Insoluble Glucan from Streptococcus mutans
变形链球菌合成不溶性葡聚糖的葡萄糖基转移酶基因克隆
- 批准号:
60570881 - 财政年份:1985
- 资助金额:
$ 9.86万 - 项目类别:
Grant-in-Aid for General Scientific Research (C)
相似国自然基金
B10细胞在改善牙周炎症中牙槽骨破坏的作用和相关机制研究
- 批准号:81570984
- 批准年份:2015
- 资助金额:57.0 万元
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牙周致病菌LPS对组织特异性单核/吞噬细胞及相应组织的致病机理研究
- 批准号:30973326
- 批准年份:2009
- 资助金额:31.0 万元
- 项目类别:面上项目
相似海外基金
L-Arg availability affects the physiological state of porphyromonas gingivalis.
L-精氨酸的可用性影响牙龈卟啉单胞菌的生理状态。
- 批准号:
10649693 - 财政年份:2022
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In vitro 3D human gingival tissue model to study oral microbiome
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10460738 - 财政年份:2021
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Calprotectin and CD69 affect regulatory T cell responses in periodontal disease
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- 批准号:
10353423 - 财政年份:2021
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In vitro 3D human gingival tissue model to study oral microbiome
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10651938 - 财政年份:2021
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In vitro 3D human gingival tissue model to study oral microbiome
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10613304 - 财政年份:2021
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