Webber R J, Zitaglio T, Hough A J
Department of Pathology, University of Arkansas for Medical Sciences, Little Rock 72205.
J Orthop Res. 1988;6(1):13-23. doi: 10.1002/jor.1100060103.
We have formulated a serum-free medium capable of supporting DNA synthesis in rabbit meniscal fibrochondrocytes at a level equivalent to 10% fetal bovine serum (FBS). The medium consists of a 1:1 mixture of Dulbecco's Modified Eagle's Medium and Ham's F-12 medium supplemented with transferrin (1 microgram/ml), selenium (1 pg/ml), trace metal mix (1:100), dexamethasone (100 ng/ml), insulin-like growth factors I and II (50 ng/ml each), pituitary fibroblast growth factor (100 ng/ml), and lactalbumin hydrolysate (2 micrograms/ml). Endothelial cell growth supplement could be substituted for lactalbumin hydrolysate to obtain similar results. Ventrex PC-1, a commercially available, low-protein, serum-free medium, was found to support proliferation of fibrochondrocytes but not as well as 10% FBS or our medium formulation. Lipid supplements, which are known to support the serum-free growth of hyaline chondrocytes, were found to be either of no value or antagonistic for the culture of fibrochondrocytes. Likewise, vitamin E alone, progesterone, putrescine, and hydrocortisone were also without benefit in our culture system. The cells had a more chondrocytic morphology when grown in defined medium as opposed to 10% FBS. The results of this study should now make it possible to identify and quantitate those factors necessary to affect meniscal repair by utilizing further techniques in vitro.
我们已经配制出一种无血清培养基,它能够支持兔半月板纤维软骨细胞的DNA合成,其水平与10%胎牛血清(FBS)相当。该培养基由杜氏改良 Eagle 培养基和哈姆氏F-12培养基按1:1混合而成,并添加了转铁蛋白(1微克/毫升)、硒(1皮克/毫升)、微量金属混合物(1:100)、地塞米松(100纳克/毫升)、胰岛素样生长因子I和II(各50纳克/毫升)、垂体成纤维细胞生长因子(100纳克/毫升)以及乳白蛋白水解物(2微克/毫升)。可用内皮细胞生长补充剂替代乳白蛋白水解物以获得相似结果。发现市售的低蛋白无血清培养基Ventrex PC-1能够支持纤维软骨细胞的增殖,但效果不如10% FBS或我们的培养基配方。已知脂质补充剂可支持透明软骨细胞的无血清生长,但发现其对纤维软骨细胞培养要么毫无价值,要么具有拮抗作用。同样,单独的维生素E、孕酮、腐胺和氢化可的松在我们的培养系统中也没有益处。与在10% FBS中培养相比,细胞在限定培养基中生长时具有更接近软骨细胞的形态。本研究结果现在应该能够通过利用进一步的体外技术来鉴定和定量那些影响半月板修复所需的因子。