Laboratoire de Pharmacologie Cellulaire de l'Ecole Pratique des Hautes Etudes, 15 rue de l'Ecole de Médecine, 75006, Paris, France.
Cytotechnology. 1995 Jan;19(1):89-94. doi: 10.1007/BF00749759.
The understanding of cartilage disorders relies on the possibility of studying mechanisms which monitor the regulation of matrix protein genes through introducing efficiently and in a reproducible manner these genes, or their regulatory regions, into cells. To this end, we attempted to improve the transfection efficiency of rabbit articular chondrocytes by the calcium phosphate procedure. Transfection efficiencies were assessed by measuring the expression of the Lac Z reporter gene encoding β-galactosidase using anin situ staining (X-gal staining) and an enzymatic assay (β-galactosidase assay).Results revealed that addition of 4 U ml(-1) of hyaluronidase before and during transfection increases by 2 to 4-fold the transfection efficiency of rabbit articular chondrocytes. Furthermore, we demonstrated that the use of a "giant" calcium phosphate DNA coprecipitate gives a higher transfection efficiency and much more reproducible results than those obtained with classical small volumes of precipitates.
软骨疾病的理解依赖于通过有效地将这些基因或其调控区引入细胞中,从而研究监测基质蛋白基因调控机制的可能性。为此,我们试图通过磷酸钙程序提高兔关节软骨细胞的转染效率。通过使用原位染色(X-gal 染色)和酶联测定法(β-半乳糖苷酶测定法)测量编码β-半乳糖苷酶的 LacZ 报告基因的表达来评估转染效率。结果表明,在转染前和转染过程中添加 4 U ml(-1)的透明质酸酶可将兔关节软骨细胞的转染效率提高 2 至 4 倍。此外,我们证明,使用“巨大”的磷酸钙 DNA 共沉淀物比使用经典的小体积沉淀物获得更高的转染效率和更可重复的结果。