Laboratory of Preclinical and Translational Research, IRCCS-CROB, Rionero in Vulture, Italy.
J Biol Regul Homeost Agents. 2013 Apr-Jun;27(2):531-41.
Response of different types of cells on biomaterials is crucial for the applications of tissue engineering and regenerative medicine. It is recognized that cell behaviour depends largely on material surface characteristics. The purpose of this study was to define the biologic response of MG63 cells to the innovative patented surface SYNTHEGRA. MG63 morphology and distribution on the three different titanium disk surfaces (sandblasted, smooth, and laser-treated) were evaluated by microscopy analysis after staining with hematoxylin and eosin. Cell adhesion was determined by crystal violet assay at 48 h while proliferation and cytotoxicity were performed by MTT assay at 24, 48, 72 and 240 h. The expression and localization of N-cadherin and beta-catenin were studied by immunofluorescence and confocal microscopy. At 48 h the adhesion was similar in all titanium surfaces, no difference in cell viability were observed in all titanium disks when compared with controls, while the cell growth on laser-treated disks was significantly higher at 240 h than at 24 and 72 h. Morphological analysis show that cells are aligned along the grooves and inside the cavities. beta-catenin signal appeared more diffuse and localized underneath the cell membrane, while N-cadherin signal was fainter in cells grown on SYNTHEGRA surface. This work put into evidence the performance of newly designed laser-micromachined surface for adhesion, growth and distribution of human osteoblast-like cells. SYNTHEGRA surface inducing modification of N-cadherin and beta-catenin expression and localization, are suggestive of cells undergoing differentiation towards osteocytes and could be particularly suited for immediate load implant procedures.
不同类型细胞对生物材料的反应对于组织工程和再生医学的应用至关重要。人们认识到,细胞行为在很大程度上取决于材料表面特性。本研究旨在定义 MG63 细胞对创新专利表面 SYNTHEGRA 的生物学反应。通过对苏木精和曙红染色后的细胞进行显微镜分析,评估了 MG63 细胞在三种不同钛盘表面(喷砂、光滑和激光处理)上的形态和分布。通过结晶紫测定法在 48 h 时测定细胞黏附,通过 MTT 测定法在 24、48、72 和 240 h 时测定增殖和细胞毒性。通过免疫荧光和共聚焦显微镜研究 N-钙黏蛋白和β-连环蛋白的表达和定位。在 48 h 时,所有钛表面的黏附情况相似,与对照组相比,所有钛盘上的细胞活力均无差异,而在激光处理盘上的细胞生长在 240 h 时明显高于 24 和 72 h。形态分析表明细胞沿凹槽排列并在空腔内。β-连环蛋白信号在细胞膜下显得更加弥散和定位,而在 SYNTHEGRA 表面生长的细胞中 N-钙黏蛋白信号较弱。这项工作证明了新设计的激光微加工表面在黏附、生长和人类成骨样细胞分布方面的性能。SYNTHEGRA 表面诱导 N-钙黏蛋白和β-连环蛋白表达和定位的改变,表明细胞正在向成骨细胞分化,可能特别适合即刻负载植入物的程序。