Lauer H C, Müller J, Gross J, Horster M F
J Periodontol. 1987 Jul;58(7):481-5. doi: 10.1902/jop.1987.58.7.481.
The effect of storage media, which are routinely used in replantation, upon the proliferative capacity of periodontal ligament fibroblasts, was compared with the effect of a tissue culture medium. The periodontal tissue was obtained from mandibular central incisors of White New Zealand rabbits. The experiments were performed in fibroblasts derived during second subculture. The storage media were physiologic salt solution, Ringer's solution and Rivanol; the tissue culture medium was alpha-minimum essential medium without nucleosides. The incubation period was 1 hour. [3H]-thymidine incorporation and cell counts were taken to indicate changes in the proliferative capacity of the fibroblasts. The tissue culture experiments showed that the proliferative ability of the periodontal ligament fibroblasts was dependent upon the composition of the storage medium. Physiologic salt solution, Ringer's solution and Rivanol were unable to maintain the metabolism of the fibroblasts. alpha-MEM medium, however, was capable of stimulating proliferation of the periodontal ligament fibroblasts.
将再植术中常规使用的储存介质对牙周膜成纤维细胞增殖能力的影响与组织培养基的影响进行了比较。牙周组织取自新西兰白兔的下颌中切牙。实验在第二代传代培养的成纤维细胞中进行。储存介质为生理盐溶液、林格氏液和利凡诺;组织培养基为不含核苷的α-最小必需培养基。孵育期为1小时。采用[3H] - 胸腺嘧啶核苷掺入法和细胞计数来指示成纤维细胞增殖能力的变化。组织培养实验表明,牙周膜成纤维细胞的增殖能力取决于储存介质的成分。生理盐溶液、林格氏液和利凡诺无法维持成纤维细胞的代谢。然而,α-MEM培养基能够刺激牙周膜成纤维细胞的增殖。