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血小板生成中的代偿机制:5-氟尿嘧啶处理的W/Wv小鼠中旁分泌反应的缺失。

Compensatory mechanisms in platelet production: lack of a paracrine response in W/Wv mice treated with 5-fluorouracil.

作者信息

Arnold J T, Radley J M, Williams N T

机构信息

Department of Physiology, University of Melbourne, Parkville, Victoria, Australia.

出版信息

Exp Hematol. 1993 Mar;21(3):414-9.

PMID:8440339
Abstract

W/Wv mice maintain normal platelet levels despite having a reduced functional stem cell pool, indicating that platelet production in these mice is compensated by altered megakaryocytopoiesis. In this study the effect of 5-fluorouracil (5-FU) treatment on platelet production in W/Wv mice and their congenic normal littermates was assessed. Recovery of circulating platelet levels occurred 11 days after 5-FU administration in W/Wv mice and subsequently did not increase above control values. In contrast, normal littermates showed an increased platelet count by day 8 and significant thrombocytosis between days 11 and 14. Investigation of bone marrow megakaryocytopoiesis in W/Wv mice showed there was no recovery in the number of megakaryocyte progenitors (CFU-Meg) per femur between days 3 and 5, but control values were reached by day 10. In addition, by day 8 the number of mature megakaryocytes per unit volume of bone marrow in these mice had not returned to control values, although the megakaryocytes were of an increased size. In comparison, the number of CFU-Meg per femur in normal mice treated with 5-FU began to recover after day 3, returned to control values by day 8 and increased to supranormal levels by day 14. Bone marrow megakaryocyte concentration was increased 2-fold over the control by day 8 and an increase in mean megakaryocyte size was also observed. The data suggest that platelet production in mice is dependent on the rate of establishment of both the progenitor cell and megakaryocyte pools. The inability of W/Wv mice to enhance and accelerate progenitor cell levels led to a reduced bone marrow response and failure to produce a marked thrombocytosis.

摘要

W/Wv小鼠尽管功能性干细胞池减少,但血小板水平维持正常,这表明这些小鼠的血小板生成通过巨核细胞生成的改变得到了补偿。在本研究中,评估了5-氟尿嘧啶(5-FU)处理对W/Wv小鼠及其同基因正常同窝仔鼠血小板生成的影响。W/Wv小鼠在给予5-FU后11天循环血小板水平开始恢复,随后未升高至对照值以上。相比之下,正常同窝仔鼠在第8天血小板计数增加,在第11天至14天之间出现明显的血小板增多。对W/Wv小鼠骨髓巨核细胞生成的研究表明,在第3天至第5天之间,每根股骨的巨核细胞祖细胞(CFU-Meg)数量没有恢复,但在第10天达到对照值。此外,到第8天,这些小鼠每单位体积骨髓中成熟巨核细胞的数量尚未恢复到对照值,尽管巨核细胞体积增大。相比之下,用5-FU处理的正常小鼠每根股骨的CFU-Meg数量在第3天后开始恢复,在第8天恢复到对照值,并在第14天增加到超正常水平。到第8天,骨髓巨核细胞浓度比对照增加了2倍,并且还观察到平均巨核细胞大小增加。数据表明,小鼠的血小板生成取决于祖细胞池和巨核细胞池的建立速率。W/Wv小鼠无法增强和加速祖细胞水平导致骨髓反应减弱,无法产生明显的血小板增多。

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