Granet C, Laroche N, Vico L, Alexandre C, Lafage-Proust M H
Laboratoire de Biologie du Tissu Osseux, Faculté de Médecine J. Lisfranc, Saint-Etienne, France.
Med Biol Eng Comput. 1998 Jul;36(4):513-9. doi: 10.1007/BF02523224.
Osteoblastic cells cultured on microcarriers in bioreactors are a potentially useful tool to reproduce the in vivo three-dimensional (3D) bone network. The aim is to compare different types of 3D and two-dimensional (2D) osteoblastic culture. ROS17/2.8 cells are cultured in a bioreactor (rotating-wall vessel) or in two kinds of control (3D petri dish, 3D Percoll) and on two types of microcarrier (Cytodex 3 and Biosilon). Growth and morphology are determined by cell count and SEM, and differentiation is determined by dosage of alkaline phosphatase (ALP) activity and northern blots (ALP and osteocalcin (OC)). SEM shows that Biosilon microcarriers are the best substrate. Proliferation in the RWV and 3D petri dish is still in the exponential phase, whereas growth in the 2D culture reaches a plateau after eight days of culture. ALP activity and the ALP and OC mRNA levels are similar at day 8 for both the RWV and 3D petri dish. However, at day 10, cells are more differentiated in the RWV. The study shows that osteoblasts are both proliferate and differentiate in 3D structures. A BrDU immunocytochemical approach shows that only the cells in the periphery of the aggregates proliferate. Therefore the bioreactor may be a suitable tissue culture model for investigation of growth and differentiation processes in tissue engineering.
在生物反应器中微载体上培养的成骨细胞是重现体内三维(3D)骨网络的一种潜在有用工具。目的是比较不同类型的3D和二维(2D)成骨细胞培养。ROS17/2.8细胞在生物反应器(旋转壁容器)或两种对照(3D培养皿、3D Percoll)中培养,并在两种类型的微载体(Cytodex 3和Biosilon)上培养。通过细胞计数和扫描电子显微镜(SEM)确定生长和形态,通过碱性磷酸酶(ALP)活性测定和Northern印迹法(ALP和骨钙素(OC))确定分化。SEM显示Biosilon微载体是最佳底物。旋转壁容器和3D培养皿中的增殖仍处于指数期,而2D培养中的生长在培养八天后达到平台期。旋转壁容器和3D培养皿在第8天时ALP活性以及ALP和OC mRNA水平相似。然而,在第10天时,旋转壁容器中的细胞分化程度更高。该研究表明成骨细胞在3D结构中既能增殖又能分化。溴脱氧尿苷免疫细胞化学方法显示只有聚集体周边的细胞增殖。因此,生物反应器可能是用于研究组织工程中生长和分化过程的合适组织培养模型。