Evidence for sodium metasilicate receptors on the human osteoblast cell surface; spatial localization and binding properties.

Q3 Biochemistry, Genetics and Molecular Biology
Molecular Membrane Biology Pub Date : 2013-12-01 Epub Date: 2013-10-23 DOI:10.3109/09687688.2013.843031
Kelly-Ann Vere, Joanna L Richens, Jordan S Lane, Helen J Harris, James Duggan, Paul O'Shea
{"title":"Evidence for sodium metasilicate receptors on the human osteoblast cell surface; spatial localization and binding properties.","authors":"Kelly-Ann Vere,&nbsp;Joanna L Richens,&nbsp;Jordan S Lane,&nbsp;Helen J Harris,&nbsp;James Duggan,&nbsp;Paul O'Shea","doi":"10.3109/09687688.2013.843031","DOIUrl":null,"url":null,"abstract":"<p><p>We report details of the interaction of sodium metasilicate with osteoblast cellular membranes using Fluoresceinphosphatidylethanolamine (FPE) as a fluorescent indicator of membrane interactions. Fluorescence imaging studies of the FPE-based indicator system revealed areas of localized binding that would be consistent with the presence of a structure with 'receptor-like' properties. From these results, it seems unlikely that silica binds 'non-specifically' to the osteoblast surface. Moreover, the receptors are localized into membrane domains. Such regions of the cell membrane could well be structures such as 'rafts' or other such localized domains within the membrane. The binding profile of silica with the osteoblast cell surface takes place with all the characteristics of a receptor-mediated process best represented by a cooperativity (sigmoidal) binding model with a Hill coefficient of 3.6.</p>","PeriodicalId":18858,"journal":{"name":"Molecular Membrane Biology","volume":" ","pages":"386-93"},"PeriodicalIF":0.0000,"publicationDate":"2013-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3109/09687688.2013.843031","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Membrane Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3109/09687688.2013.843031","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2013/10/23 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0

Abstract

We report details of the interaction of sodium metasilicate with osteoblast cellular membranes using Fluoresceinphosphatidylethanolamine (FPE) as a fluorescent indicator of membrane interactions. Fluorescence imaging studies of the FPE-based indicator system revealed areas of localized binding that would be consistent with the presence of a structure with 'receptor-like' properties. From these results, it seems unlikely that silica binds 'non-specifically' to the osteoblast surface. Moreover, the receptors are localized into membrane domains. Such regions of the cell membrane could well be structures such as 'rafts' or other such localized domains within the membrane. The binding profile of silica with the osteoblast cell surface takes place with all the characteristics of a receptor-mediated process best represented by a cooperativity (sigmoidal) binding model with a Hill coefficient of 3.6.

人成骨细胞表面存在偏硅酸钠受体的证据空间定位和绑定属性。
我们使用荧光磷脂酰乙醇胺(FPE)作为膜相互作用的荧光指示剂,报道了偏硅酸钠与成骨细胞细胞膜相互作用的细节。基于fpe的指示剂系统的荧光成像研究显示了局部结合区域,这与具有“受体样”性质的结构的存在是一致的。从这些结果来看,二氧化硅似乎不太可能“非特异性”地与成骨细胞表面结合。此外,受体定位于膜结构域。细胞膜的这些区域很可能是细胞膜内的结构,如“筏”或其他类似的局部区域。二氧化硅与成骨细胞表面的结合具有受体介导过程的所有特征,最好的代表是希尔系数为3.6的协同性(s形)结合模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Molecular Membrane Biology
Molecular Membrane Biology 生物-生化与分子生物学
CiteScore
4.80
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Cessation. Molecular Membrane Biology provides a forum for high quality research that serves to advance knowledge in molecular aspects of biological membrane structure and function. The journal welcomes submissions of original research papers and reviews in the following areas: • Membrane receptors and signalling • Membrane transporters, pores and channels • Synthesis and structure of membrane proteins • Membrane translocation and targeting • Lipid organisation and asymmetry • Model membranes • Membrane trafficking • Cytoskeletal and extracellular membrane interactions • Cell adhesion and intercellular interactions • Molecular dynamics and molecular modelling of membranes. • Antimicrobial peptides.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信