IR@PKUHSC  > 北京大学药学院  > 化学生物学系
学科主题药学
Integrin-mediated signaling contributes to gadolinium-containing-particle-promoted cell survival and G(1) to S phase cell cycle transition by enhancing focal adhesion formation
Li, Jin-Xia1,2; Fu, Li-Juan1; Yang, Xiao-Gai1; Wang, Kui1,2
关键词Gadolinium Integrin Focal Adhesion Nephrogenic Systemic Fibrosis Cell Proliferation
刊名JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY
2012-03-01
DOI10.1007/s00775-011-0859-7
17期:3页:375-385
收录类别SCI
文章类型Article
WOS标题词Science & Technology
类目[WOS]Biochemistry & Molecular Biology ; Chemistry, Inorganic & Nuclear
资助者National Natural Science Foundation of China ; National Natural Science Foundation of China
研究领域[WOS]Biochemistry & Molecular Biology ; Chemistry
关键词[WOS]NEPHROGENIC SYSTEMIC FIBROSIS ; GROWTH-FACTOR RECEPTOR ; IMAGING CONTRAST AGENTS ; RARE-EARTH ELEMENTS ; DEPENDENT REGULATION ; EPITHELIAL-CELLS ; STRUCTURAL BASIS ; ACTIVATION ; PROLIFERATION ; FIBROBLASTS
英文摘要

We previously reported that Gd-containing particles formed under physiological conditions act as active entities to enhance cell survival and promote S phase entry via activation of both mitogen-activated protein kinase/extracellular-signal-regulated protein kinase (ERK) and phosphatidylinositol 3-kinase/Akt signaling pathways. However, how they transduce the extracellular signal inside the cell remains unclear. The present study demonstrates that Gd-containing particles can alleviate serum-deprivation-induced cell death and promote G(1) to S phase cell cycle progression by enhancing cell adhesion to the extracellular matrix. As an indicator of adhesion, the vinculin distribution was detected by confocal laser scanning microscopy. The control cells exhibited fewer and less typical focal adhesions. After treatment with Gd-containing particles, a large number of vinculin-containing focal adhesions were maintained. In the presence of integrin antagonists, the percentage of S phase entry induced by Gd-containing particles was decreased and the enhancement of cell viability was also attenuated, along with a decrease in both cyclin D expression and ERK phosphorylation. In summary, the present results suggest that the integrin-mediated signaling pathway plays an important role in cell survival and G(1) to S phase transition promoted by Gd-containing particles by enhancing focal adhesion formation. The results presented here provide novel evidence to advance knowledge leading to further understanding of the mechanisms of both cell proliferation and cell survival promoted by Gd and may be helpful for developing effective measures to prevent or treat nephrogenic systemic fibrosis.

语种英语
所属项目编号20637010
资助者National Natural Science Foundation of China ; National Natural Science Foundation of China
WOS记录号WOS:000301186000005
引用统计
被引频次:7[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.bjmu.edu.cn/handle/400002259/54291
专题北京大学药学院_化学生物学系
作者单位1.Peking Univ, Dept Biol Chem, Sch Pharmaceut Sci, Beijing 100191, Peoples R China
2.Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China
推荐引用方式
GB/T 7714
Li, Jin-Xia,Fu, Li-Juan,Yang, Xiao-Gai,et al. Integrin-mediated signaling contributes to gadolinium-containing-particle-promoted cell survival and G(1) to S phase cell cycle transition by enhancing focal adhesion formation[J]. JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY,2012,17(3):375-385.
APA Li, Jin-Xia,Fu, Li-Juan,Yang, Xiao-Gai,&Wang, Kui.(2012).Integrin-mediated signaling contributes to gadolinium-containing-particle-promoted cell survival and G(1) to S phase cell cycle transition by enhancing focal adhesion formation.JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY,17(3),375-385.
MLA Li, Jin-Xia,et al."Integrin-mediated signaling contributes to gadolinium-containing-particle-promoted cell survival and G(1) to S phase cell cycle transition by enhancing focal adhesion formation".JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY 17.3(2012):375-385.
条目包含的文件
条目无相关文件。
个性服务
推荐该条目
保存到收藏夹
查看访问统计
导出为Endnote文件
谷歌学术
谷歌学术中相似的文章
[Li, Jin-Xia]的文章
[Fu, Li-Juan]的文章
[Yang, Xiao-Gai]的文章
百度学术
百度学术中相似的文章
[Li, Jin-Xia]的文章
[Fu, Li-Juan]的文章
[Yang, Xiao-Gai]的文章
必应学术
必应学术中相似的文章
[Li, Jin-Xia]的文章
[Fu, Li-Juan]的文章
[Yang, Xiao-Gai]的文章
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。