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小鼠多能造血祖细胞数量的一种调节机制。

A regulatory mechanism for the number of pluripotential haemopoietic progenitor cells in mice.

作者信息

Blackett N M, Botnick L E

出版信息

Blood Cells. 1981;7(2):417-43.

PMID:7296010
Abstract

Large changes in the pattern of regeneration of haemopoietic progenitor cells (CFU-S) are reported as a result of simply altering the time interval between administration of certain cytotoxic agents and whole-body irradiation. These results suggest a negative feedback control for the number of CFU-S, which has an appreciable time delay. A high inverse correlation between the number of maturing granulocytic cells (with ring-shaped nuclei) at the time of irradiation and the subsequent regeneration of CFU-S is consistent with these cells producing some substance that controls the number but not the proliferation rate of the CFU-S. The possibility is considered that this mechanism is an important control in the biological regulation of haemopoiesis.

摘要

据报道,仅仅改变某些细胞毒性药物给药与全身照射之间的时间间隔,造血祖细胞(CFU-S)的再生模式就会发生巨大变化。这些结果表明,CFU-S数量存在负反馈控制,且具有明显的时间延迟。照射时成熟粒细胞(核呈环状)数量与随后CFU-S的再生之间存在高度负相关,这与这些细胞产生某种控制CFU-S数量而非增殖速率的物质是一致的。人们认为这种机制可能是造血生物学调节中的一种重要控制方式。

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A regulatory mechanism for the number of pluripotential haemopoietic progenitor cells in mice.小鼠多能造血祖细胞数量的一种调节机制。
Blood Cells. 1981;7(2):417-43.
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Studies of W mutant mice provide evidence for alternate mechanisms capable of activating hematopoietic stem cells.对W突变小鼠的研究为能够激活造血干细胞的替代机制提供了证据。
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Self-maintenance capacity of CFU-S.脾集落形成单位(CFU-S)的自我维持能力
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Mol Syst Biol. 2009;5:293. doi: 10.1038/msb.2009.49. Epub 2009 Jul 28.
2
A new approach to the evolution of the blastic crisis from chronic myelocytic leukemia: dynamic interplay of cellular alterations and a changing microenvironment.慢性粒细胞白血病急变期演变的一种新方法:细胞改变与不断变化的微环境之间的动态相互作用。
EMBO J. 1986 Apr;5(4):671-7. doi: 10.1002/j.1460-2075.1986.tb04266.x.