Neben S, Anklesaria P, Greenberger J, Mauch P
Joint Center for Radiation Therapy, Harvard Medical School, Boston, MA.
Exp Hematol. 1993 Mar;21(3):438-43.
Murine hematopoietic stem cells with varying proliferative capacity can be assayed by limiting dilution analysis of "cobblestone area" (CA) formation on stromal layers in microlong-term bone marrow cultures. Cobblestone area forming cell (CAFC) frequency determined at early time points (day 7) correlates with mature stem cells measured as day 8 CFU-S, whereas CAFC frequency determined at day 28 correlates more closely with long-term marrow repopulating ability. Here we report a modification of the CAFC assay in which a clonal bone marrow stromal cell line, GB1/6, is substituted for fresh marrow-derived stromal layers. This modification simplifies the initial culture setup, eliminates inhomogeneities in the stromal layer and reduces the need for mice. Normal bone marrow CAFC frequencies were the same for both types of stromal cell underlayer, demonstrating the ability of a clonal cell line to completely replace the heterogeneous microenvironment of fresh stroma for in vitro stem cell support.
具有不同增殖能力的小鼠造血干细胞,可以通过对微型长期骨髓培养中基质层上“卵石区域”(CA)形成进行极限稀释分析来检测。在早期时间点(第7天)测定的卵石区域形成细胞(CAFC)频率与作为第8天脾集落形成单位(CFU-S)测定的成熟干细胞相关,而在第28天测定的CAFC频率与长期骨髓重建能力更密切相关。在此,我们报告了对CAFC检测方法的一种改进,其中用克隆骨髓基质细胞系GB1/6替代新鲜骨髓来源的基质层。这种改进简化了初始培养设置,消除了基质层的不均匀性,并减少了对小鼠的需求。两种类型的基质细胞底层培养出的正常骨髓CAFC频率相同,这表明克隆细胞系能够完全替代新鲜基质的异质性微环境,为体外干细胞提供支持。