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秋水仙酰胺诱导弗氏红白血病细胞内复制后,其巨核样细胞倍性增加。

Megakaryocyte-like increase in ploidy of Friend's erythroleukemia cells induced to endoreplication by colcemid.

作者信息

Paoletti F, Mocali A, Cellai C, Caporale R, Vannucchi A M

机构信息

Istituto di Patologia Generale, Università degli Studi di Firenze, Florence, Italy.

出版信息

Exp Hematol. 1996 Oct;24(12):1441-8.

PMID:8913291
Abstract

Previous work from this laboratory has shown that Friend's murine erythroleukemia cells (MELCs) express some bio-chemical traits of the megakaryocytic lineage. The supposed mixed erythroid/megakaryocytic nature of these cells has been investigated further by challenging MELCs with the antimicrotubule agent colcemid. This compound, at the concentration of 40 nM, was found to induce a striking arrest of cell growth without significant effects on viability. At the same time, the bulk of treated MELCs underwent a large increase in size to contain, after 3 days, as much as 4 times more proteins and 5 times more DNA than controls. As shown by high rates of 3H-thymidine incorporation, increase in DNA content was the result of active synthesis without completion of intervening mitosis according to a process that closely resembled endoreplication. Eventually, colcemidinduced MELCs presented multilobed nuclei and were arranged into discrete ploidy groups containing up to 16 N levels of DNA. Moreover, upon colcemid addition, MELCs initiated a polyploid response that was shown to continue, even in the absence of the inducer, to yield cells that became strongly positive for acetylcholinesterase (AChE) in the late stages of culture. These effects were compatible with a colcemid-induced commitment of MELCs to megakaryocyte differentiation, for which these cells seemed to be definitely programmed. The expression of megakaryocyte features in MELCs provided further evidence for the bipotentiality (erythroid/megakaryocytic) of this model.

摘要

本实验室先前的研究表明,弗瑞德小鼠红白血病细胞(MELCs)表达巨核细胞系的一些生化特征。通过用抗微管药物秋水仙酰胺处理MELCs,对这些细胞假定的红系/巨核系混合性质进行了进一步研究。发现该化合物在浓度为40 nM时可显著抑制细胞生长,而对细胞活力无明显影响。同时,大部分经处理的MELCs体积大幅增大,3天后其蛋白质含量比对照多4倍,DNA含量比对照多5倍。如高比率的3H-胸腺嘧啶核苷掺入所示,DNA含量的增加是活跃合成的结果,中间没有完成有丝分裂,这一过程与核内复制非常相似。最终,秋水仙酰胺诱导的MELCs呈现多叶核,并被分成不同的倍体组,DNA水平高达16N。此外,添加秋水仙酰胺后,MELCs启动了多倍体反应,即使在没有诱导剂的情况下,该反应仍会继续,产生在培养后期对乙酰胆碱酯酶(AChE)呈强阳性的细胞。这些效应与秋水仙酰胺诱导MELCs向巨核细胞分化的作用相一致,这些细胞似乎确实已被编程为此种分化。MELCs中巨核细胞特征的表达为该模型的双潜能性(红系/巨核系)提供了进一步的证据。

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