Gillery P, Bonnet A, Borel J P
Laboratory of Biochemistry, CNRS ERS 0017, Faculty of Medicine, University of Reims-Champagne-Ardenne, France.
Anal Biochem. 1993 May 1;210(2):374-7. doi: 10.1006/abio.1993.1210.
A fast and sensitive in situ assay of deoxyribonucleic acid in miniaturized lattice cultures of fibroblasts is described. Tridimensional collagen and fibrin lattices prepared in 24-well plates were seeded with 50,000 to 200,000 cells. Cultures were fixed with formaldehyde, rinced with isopropanol, and dried. DNA assay was performed directly in the wells by addition of 3,5-diaminobenzoic acid (DABA) reagent. A calibration curve was prepared with calf thymus DNA. Fluorescence of DNA-DABA was evaluated after 45 min incubation (excitation wavelength 420 nm, emission wavelength 490 nm). The method showed linear results from 0.5 to 10 micrograms DNA and proved sensitive for low cell numbers (50,000 per dish). DNA assay in monolayers and in different types of lattices showed that comparable results were obtained in the different models without interference of the extracellular matrix. This technique is regarded as a costless and efficient tool for evaluating the number of cells in lattices in basal conditions or under pharmacological stimulation.
本文描述了一种在成纤维细胞小型化格子培养物中对脱氧核糖核酸进行快速灵敏的原位测定方法。在24孔板中制备的三维胶原蛋白和纤维蛋白格子接种了50000至200000个细胞。培养物用甲醛固定,用异丙醇冲洗并干燥。通过添加3,5-二氨基苯甲酸(DABA)试剂直接在孔中进行DNA测定。用小牛胸腺DNA制备校准曲线。孵育45分钟后评估DNA-DABA的荧光(激发波长420nm,发射波长490nm)。该方法在0.5至10微克DNA范围内显示出线性结果,并且对低细胞数量(每皿50000个)证明是灵敏的。单层和不同类型格子中的DNA测定表明,在不同模型中获得了可比结果,且不受细胞外基质的干扰。该技术被认为是一种在基础条件或药理刺激下评估格子中细胞数量的低成本且高效的工具。