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阿那格雷对人类巨核细胞生成的影响。

The effects of anagrelide on human megakaryocytopoiesis.

作者信息

Solberg L A, Tefferi A, Oles K J, Tarach J S, Petitt R M, Forstrom L A, Silverstein M N

机构信息

Division of Hematology/Oncology, Mayo Clinic Jacksonville, Florida 32224, U.S.A.

出版信息

Br J Haematol. 1997 Oct;99(1):174-80. doi: 10.1046/j.1365-2141.1997.3503164.x.

Abstract

Anagrelide, an inhibitor of platelet aggregation, decreases the number of platelets in normal subjects and in patients with myeloproliferative disorders. We describe studies aimed at discovering the general mechanism(s) by which anagrelide acts. We examined three hypotheses: (1) anagrelide shortens platelet survival, (2) anagrelide inhibits the proliferation of megakaryocytic-committed progenitor cells (CFU-M), and (3) anagrelide inhibits maturation of megakaryocytes. We observed that anagrelide did not shorten platelet survival. Proliferation of CFU-M in vivo was not affected by anagrelide, although high concentrations of anagrelide inhibited CFU-M in vitro. In-vivo and in-vitro anagrelide altered the maturation of megakaryocytes, causing a decrease in their size and changing other morphometric features. We conclude that anagrelide decreases the number of platelets primarily by interfering with the maturation of megakaryocytes.

摘要

阿那格雷是一种血小板聚集抑制剂,可减少正常受试者和骨髓增殖性疾病患者的血小板数量。我们描述了旨在发现阿那格雷作用的一般机制的研究。我们检验了三个假设:(1)阿那格雷缩短血小板生存期;(2)阿那格雷抑制巨核细胞定向祖细胞(CFU-M)的增殖;(3)阿那格雷抑制巨核细胞成熟。我们观察到阿那格雷并未缩短血小板生存期。阿那格雷对体内CFU-M的增殖没有影响,尽管高浓度的阿那格雷在体外可抑制CFU-M。体内和体外的阿那格雷均改变了巨核细胞的成熟,导致其大小减小并改变了其他形态学特征。我们得出结论,阿那格雷主要通过干扰巨核细胞的成熟来减少血小板数量。

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