Koury M J, Krantz S B
Cell Tissue Kinet. 1982 Jan;15(1):59-67. doi: 10.1111/j.1365-2184.1982.tb01024.x.
The primitive burst-forming unit-erythroid (BFU-e) derived from normal and regenerating murine bone marrow was examined by velocity sedimentation at unit gravity. An increase in the modal sedimentation velocity and the percentage of rapidly sedimenting BFU-e was found in regenerating marrow as compared to normal marrow. Neither hypertransfusion-induced plethora nor administration of erythropoietin (Ep) during regeneration altered the changes from normal in the velocity sedimentation profile observed during regeneration. Separated marrow cells were pooled as rapidly sedimenting and slowly sedimenting and then examined for percentage of BFU-e in DNA synthesis and growth response in vitro to increasing concentrations of a partially purified Ep preparation. The percentage of BFU-e in DNA synthesis as determined by tritiated thymidine killing does not correspond to the BFU-e growth response to Ep in vitro. No difference in growth was noted between BFU-e from rapidly and slowly sedimenting normal marrow cells despite an increased percentage in DNA synthesis of normal BFU-e which sedimented rapidly. No significant difference in the percentage of BFU-e in DNA synthesis was found between the rapidly and slowly sedimenting subpopulations of regenerating BFU-e, but the latter had a reduced growth response to low concentrations of Ep.
采用单位重力下的速度沉降法,对源自正常和再生小鼠骨髓的原始红细胞爆式集落形成单位(BFU-e)进行了检测。与正常骨髓相比,再生骨髓中BFU-e的模态沉降速度以及快速沉降的BFU-e百分比均有所增加。再生过程中,超输血引起的多血症以及促红细胞生成素(Ep)的给药均未改变再生过程中观察到的速度沉降曲线相对于正常情况的变化。将分离的骨髓细胞分为快速沉降和缓慢沉降两组,然后检测DNA合成中BFU-e的百分比以及体外对不同浓度部分纯化的Ep制剂的生长反应。通过氚标记胸腺嘧啶核苷杀伤法测定的DNA合成中BFU-e的百分比与体外BFU-e对Ep的生长反应并不对应。尽管快速沉降的正常BFU-e的DNA合成百分比有所增加,但快速沉降和缓慢沉降的正常骨髓细胞来源的BFU-e在生长方面未观察到差异。再生BFU-e的快速沉降和缓慢沉降亚群在DNA合成中BFU-e的百分比没有显著差异,但后者对低浓度Ep的生长反应降低。