Quinn L S, Nameroff M
Differentiation. 1983;24(2):124-30. doi: 10.1111/j.1432-0436.1983.tb01311.x.
Immunocytochemical analysis of small myogenic clones was used to compare the effects of fresh medium (FM) and conditioned medium (CM) on muscle differentiation. In order to compare the same population of cells, clones were initiated in FM and then switched to either new FM or to CM. Clones were fixed at 12-hour intervals up to 76 hours, then assayed for the presence of post-mitotic myoblasts by immunoperoxidase staining for muscle myosin heavy chain (MHC) or M-creatine kinase (MCK). In both media, myogenic cells occurred predominantly in homogeneous positive clones (all cells (MHC +/MCK +) which contained 2" cells. At 76 hours, the percentages of 1-, 2-, and 4-cell positive clones did not differ statistically in the two conditions; however, the percentages of 8- and 16-cell positive clones were significantly reduced in CM, and the percentages of small negative clones were concomitantly increased. We conclude from these data that CM affects myogenesis by slowing progression through a predetermined lineage rather than by changing the number of mitoses an individual cell will undergo before terminally differentiating. These results further support the idea that progress through the myogenic lineage is mediated by cell divisions.
利用小肌源性克隆的免疫细胞化学分析来比较新鲜培养基(FM)和条件培养基(CM)对肌肉分化的影响。为了比较相同的细胞群体,在FM中启动克隆,然后切换到新的FM或CM。每隔12小时固定克隆直至76小时,然后通过免疫过氧化物酶染色检测肌肉肌球蛋白重链(MHC)或M-肌酸激酶(MCK),以确定有丝分裂后成肌细胞的存在。在两种培养基中,肌源性细胞主要出现在均匀阳性克隆中(所有细胞(MHC +/MCK +),其中包含2" 细胞)。在76小时时,两种条件下1、2和4细胞阳性克隆的百分比在统计学上没有差异;然而,CM中8和16细胞阳性克隆的百分比显著降低,小阴性克隆的百分比相应增加。从这些数据中我们得出结论,CM通过减缓通过预定谱系的进程来影响肌生成,而不是通过改变单个细胞在终末分化前将经历的有丝分裂次数。这些结果进一步支持了通过肌源性谱系的进程是由细胞分裂介导的这一观点。