Pretlow T G, Williams E E, Davis M L, Zettergren J G
Am J Pathol. 1973 Aug;72(2):201-20.
Spleen colony forming cells (CFU-S) from mouse bone marrow were concentrated using velocity sedimentation in an isokinetic gradient of Ficoll (polysucrose) in tissue culture medium. Following separation, CFU-S were found as a sharp modal population of cells which was discrete from the modal populations of lymphocytes and other cell types. Despite the wide separation of lymphocytes, granulocytes and CFU-S in the density gradient, there was no appreciable resolution of CFU-S specifically committed to erythroid, granulocytic or undifferentiated colony formation. This suggests that committed stem cells either share identical physical properties or are not detected by the spleen colony assay. In the purest fractions from the isokinetic gradient, CFU-S were 2.8- to 4.7-fold purified when compared with mouse bone marrow before separation.
利用组织培养基中菲可(聚蔗糖)等速梯度的速度沉降法对小鼠骨髓中的脾集落形成细胞(CFU-S)进行浓缩。分离后,CFU-S表现为一个清晰的模态细胞群体,与淋巴细胞和其他细胞类型的模态群体不同。尽管在密度梯度中淋巴细胞、粒细胞和CFU-S被广泛分离,但对于特异性致力于红系、粒系或未分化集落形成的CFU-S并没有明显的分辨。这表明定向干细胞要么具有相同的物理特性,要么无法通过脾集落测定法检测到。在等速梯度的最纯组分中,与分离前的小鼠骨髓相比,CFU-S的纯度提高了2.8至4.7倍。