Morgan J E
Department of Histopathology, Charing Cross and Westminster Medical School, London, U.K.
J Neurol Sci. 1988 Jun;85(2):197-207. doi: 10.1016/0022-510x(88)90156-6.
Mouse muscle cells, obtained by enzymatically disaggregating newborn mouse muscle, were separated on a discontinuous Percoll gradient. The myogenicity in vitro of the resultant cell fractions was examined by counting the percentage of nuclei in myotubes. Myogenicity in vivo was assessed by implanting a cell suspension of one of the allotypes of glucose-6-phosphate isomerase (GPI) into a regenerating skeletal muscle graft of a second GPI allotype: the finding of hybrid GPI indicated that the implanted cells were myogenic. Separation of mouse muscle cells on a discontinuous Percoll gradient gave rise to two myogenic fractions, one of which was more myogenic in vitro than were the unseparated cells and one of which was less myogenic. Both of these fractions were myogenic in vivo. A cell fraction was also produced which was non-myogenic in vitro as well as in vivo. In vitro and in vivo measurements of myogenicity were therefore in broad agreement.
通过酶解新生小鼠肌肉获得的小鼠肌肉细胞,在不连续的Percoll梯度上进行分离。通过计数肌管中细胞核的百分比来检测所得细胞组分的体外成肌能力。通过将葡萄糖-6-磷酸异构酶(GPI)的一种同种异型的细胞悬液植入第二种GPI同种异型的再生骨骼肌移植物中来评估体内成肌能力:发现杂交GPI表明植入的细胞具有成肌性。在不连续的Percoll梯度上分离小鼠肌肉细胞产生了两个成肌组分,其中一个在体外比未分离的细胞更具成肌性,另一个则成肌性较差。这两个组分在体内均具有成肌性。还产生了一个在体外和体内均无成肌性的细胞组分。因此,体外和体内成肌能力的测量结果大致一致。