Wright E G, Lorimore S A
Department of Anatomy and Experimental Pathology, University of St Andrews, Scotland.
Cell Tissue Kinet. 1987 May;20(3):301-10. doi: 10.1111/j.1365-2184.1987.tb01312.x.
In marrow from Sl/Sld mice (but not +/+ mice) day 7 and day 8 CFU-S proliferate whilst day 10 and day 12 CFU-S exhibit negligible proliferation. Media conditioned by both +/+ and Sl/Sld marrow contains an inhibitor of CFU-S proliferation but day 8 CFU-S in +/+ and Sl/Sld marrow show marked dose-response differences to this factor. To inhibit the proliferation of Sl/Sld CFU-S required approximately ten times the concentration of inhibitor that inhibited the proliferation of +/+ CFU-S. Thus abnormally responsive day 8-CFU-S were shown to proliferate in an inhibitory environment. Abnormalities in Sl/Sld CFU-S function were also demonstrated in heterotopic transplantation experiments using +/+ and Sl/Sld donors and hosts to obtain ectopic bone marrow with various stromal (donor) and haemopoietic (host) combinations. Day 8 Sl/Sld CFU-S were seen to proliferate, irrespective of whether the stromal environment was derived from Sl/Sld or +/+ marrow. Sl/Sld mice are generally regarded as animals in which there is a genetically determined defect in haemopoiesis due to an abnormality in the haemopoietic environment. It is difficult, however, to attribute the abnormal CFU-S behaviour in these experiments to environmental factors and the results are consistent with mutation at the Sl locus affecting the responses of CFU-S to regulatory signals, i.e. the genetic defect is not confined to the stromal environment.
在 Sl/Sld 小鼠(而非 +/+ 小鼠)的骨髓中,第 7 天和第 8 天的脾集落形成单位(CFU-S)会增殖,而第 10 天和第 12 天的 CFU-S 增殖可忽略不计。由 +/+ 和 Sl/Sld 骨髓条件培养液均含有 CFU-S 增殖抑制剂,但 +/+ 和 Sl/Sld 骨髓中的第 8 天 CFU-S 对该因子显示出明显的剂量反应差异。抑制 Sl/Sld CFU-S 的增殖所需的抑制剂浓度约为抑制 +/+ CFU-S 增殖所需浓度的十倍。因此,异常反应性的第 8 天 CFU-S 被证明在抑制环境中增殖。在异位移植实验中也证明了 Sl/Sld CFU-S 功能异常,该实验使用 +/+ 和 Sl/Sld 供体及宿主,以获得具有各种基质(供体)和造血(宿主)组合的异位骨髓。无论基质环境是源自 Sl/Sld 还是 +/+ 骨髓,都可见第 8 天的 Sl/Sld CFU-S 增殖。Sl/Sld 小鼠通常被视为由于造血环境异常而在造血方面存在遗传决定缺陷的动物。然而,很难将这些实验中 CFU-S 的异常行为归因于环境因素,其结果与 Sl 位点的突变影响 CFU-S 对调节信号的反应一致,即遗传缺陷并不局限于基质环境。