首页> 外文期刊>ACS applied materials & interfaces >Different Organization of Type I Collagen Immobilized on Silanized and Nonsilanized Titanium Surfaces Affects Fibroblast Adhesion and Fibronectin Secretion
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Different Organization of Type I Collagen Immobilized on Silanized and Nonsilanized Titanium Surfaces Affects Fibroblast Adhesion and Fibronectin Secretion

机译:固定在硅烷化和非硅烷化钛表面上的I型胶原蛋白的不同组织影响成纤维细胞粘附和纤连蛋白分泌

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Silanization has emerged in recent years as a way to obtain a stronger and more stable attachment of biomolecules to metallic substrates. However, its impact on protein conformation, a key aspect that influences cell response, has hardly been studied. In this work, we analyzed by atomic force microscopy (AFM) the distribution and conformation of type I collagen on plasma-treated surfaces before and after silanization. Subsequently, we investigated the effect of the different collagen conformations on fibroblasts adhesion and fibronectin secretion by immunofluorescence analyses. Two different organosilanes were used on plasma-treated titanium surfaces, either 3-chloropropyl-triethoxy-silane (CPTES) or 3-glycidyloxypropyltriethoxy-silane (GPTES). The properties and amount of the adsorbed collagen were assessed by contact angle, X-ray photoelectron spectroscopy, optical waveguide lightmode spectroscopy, and AFM. AFM studies revealed different conformations of type I collagen depending on the silane employed. Collagen was organized in fibrillar networks over very hydrophilic (plasma treated titanium) or hydrophobic (silanized with CPTES) surfaces, the latter forming little globules with a beads-on-a-string appearance, whereas over surfaces presenting an intermediate hydrophobic character (silanized with GPTES), collagen was organized into clusters with a size increasing at higher protein concentration in solution. Cell response was strongly affected by collagen conformation, especially at low collagen density. The samples exhibiting collagen organized in globular clusters (GPTES-functionafized samples) favored a faster and better fibroblast adhesion as well as better cell spreading, focal adhesions formation, and more pronounced fibronectin fibrillogenesis. In contrast, when a certain protein concentration was reached at the material surface, the effect of collagen conformation was masked, and similar fibroblast response was observed in all samples.
机译:近年来,硅烷化已成为一种使生物分子更牢固,更稳定地附着在金属基质上的方法。然而,几乎没有研究其对蛋白质构象的影响,而蛋白质构象是影响细胞反应的关键方面。在这项工作中,我们通过原子力显微镜(AFM)分析了硅烷化前后等离子体处理过的表面上I型胶原的分布和构象。随后,我们通过免疫荧光分析研究了不同胶原构象对成纤维细胞粘附和纤连蛋白分泌的影响。在等离子体处理过的钛表面上使用了两种不同的有机硅烷,即3-氯丙基-三乙氧基硅烷(CPTES)或3-环氧丙氧基丙基三乙氧基硅烷(GPTES)。通过接触角,X射线光电子能谱,光波导光模能谱和AFM来评估吸附的胶原蛋白的性质和量。 AFM研究表明,取决于所用的硅烷,I型胶原蛋白的构象不同。胶原蛋白在非常亲水的表面(经等离子体处理的钛)或疏水的表面(经CPTES硅烷化)形成纤维状网络,后者形成的小球状串珠状,而在表面表现出中等的疏水性(经硅烷化处理) GPTES),胶原蛋白被组织成簇,并且随着溶液中蛋白质浓度的增加其大小增加。细胞反应受到胶原构象的强烈影响,尤其是在低胶原密度下。表现出呈球形簇组织的胶原蛋白的样品(GPTES功能化样品)有利于更快,更好的成纤维细胞粘附以及更好的细胞扩散,粘着斑形成和更明显的纤连蛋白原纤维形成。相反,当在材料表面达到一定的蛋白质浓度时,胶原构象的作用被掩盖,并且在所有样品中观察到相似的成纤维细胞反应。

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