Gordon M Y, Blackett N M, Douglas I D
Br J Haematol. 1975 Sep;31(1):103-10. doi: 10.1111/j.1365-2141.1975.tb00837.x.
A technique which allows colony growth of haematologically normal human bone marrow cells is described. The cells are supported by semi-solid-agar-medium inside modified Millipore diffusion chambers implanted in the peritoneal cavity of irradiated mice. After 9 days incubation colonies containing up to 1000 cells are found in these Agar Diffusion Chambers. All haematologically normal patients studied so far produced colonies, the majority with between 10 and 40 colonies per 2 X 10(5) bone marrow cells inoculated. This culture system therefore provides a convenient and reliable clonal assay for human bone marrow cells which, in contrast to the agar colony assay in vitro, does not require a source of Colony Stimulating Factor (CSF).
本文描述了一种能使血液学正常的人类骨髓细胞形成集落生长的技术。细胞由植入受辐照小鼠腹腔内的改良微孔扩散小室中的半固体琼脂培养基支持。孵育9天后,在这些琼脂扩散小室中发现了含有多达1000个细胞的集落。迄今为止研究的所有血液学正常的患者都产生了集落,大多数患者每接种2×10⁵个骨髓细胞可形成10至40个集落。因此,与体外琼脂集落测定法不同,该培养系统为人类骨髓细胞提供了一种方便可靠的克隆测定方法,且不需要集落刺激因子(CSF)来源。