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
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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.

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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。
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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.
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