Haemopoietic stem cell proliferation in the bone marrow of S1/S1d mice.

E G Wright, S A Lorimore
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引用次数: 5

Abstract

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.

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造血干细胞在S1/S1d小鼠骨髓中的增殖。
在Sl/Sld小鼠(但不包括+/+小鼠)的骨髓中,第7天和第8天CFU-S增殖,而第10天和第12天CFU-S增殖可忽略不计。+/+和Sl/Sld骨髓培养基均含有CFU-S增殖抑制剂,但第8天,+/+和Sl/Sld骨髓中的CFU-S对该因子表现出明显的剂量反应差异。为了抑制Sl/Sld CFU-S的增殖,需要大约10倍于抑制+/+ CFU-S增殖的抑制剂浓度。因此,异常反应的day 8-CFU-S显示在抑制环境中增殖。在异位移植实验中,使用+/+和Sl/Sld供体和宿主获得不同基质(供体)和造血(宿主)组合的异位骨髓,也证实了Sl/Sld CFU-S功能的异常。无论基质环境是来自Sl/Sld还是+/+骨髓,第8天的CFU-S都能增殖。Sl/Sld小鼠通常被认为是由于造血环境异常而存在遗传决定的造血缺陷的动物。然而,很难将这些实验中CFU-S的异常行为归因于环境因素,结果与影响CFU-S对调节信号反应的Sl位点突变一致,即遗传缺陷并不局限于间质环境。
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Abstracts of the joint meeting of the Cell Kinetics Society and the International Cell Cycle Society. 28-31 March 1990, St Louis, Missouri, U.S.A. Abstracts of the 16th meeting of the European Study Group for Cell Proliferation. 3-6 May 1989, Milan. Proceedings of the Cell Kinetics Society, thirteenth annual meeting. 29 March-1 April 1989, White Plains, New York, U.S.A. Bone marrow fibroblast colony-forming cells are osteogenic stem cells. Epidermal tissue homeostasis. III. Effect of hydrocortisone on cell pool size, cell birth rate and cell loss in normal toads and in toads deprived of the pars distalis of the pituitary gland.
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