5-Aza-2'-deoxycytidine-induced cytotoxicity and limb reduction defects in the mouse.

Teratology Pub Date : 2002-04-01 DOI:10.1002/TERA.10029
M. Rosen, N. Chernoff
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引用次数: 10

Abstract

BACKGROUND 5-Aza-2'-deoxycytidine (dAZA), causes hindlimb phocomelia in CD-1 mice. Studies in our laboratory have examined the hypothesis that compound- induced changes in gene expression may uniquely affect hindlimb pattern formation. The present study tests the hypothesis that dAZA causes limb dysplasia by inducing cytotoxicity among rapidly proliferating cells in the limb bud mesenchyme. METHODS Pregnant CD-1 mice were given a teratogenic dose of dAZA (i.p.) at different times on GD 10 and fetuses evaluated for skeletal development in both sets of limbs by standard methods. Using general histology and BrdU immunohistochemistry, limb mesenchymal cell death and cell proliferation were then assessed in embryos at various times post dosing, shortly after initial limb bud outgrowth. The effect of dAZA on early limb chondrogenesis was also studied using Northern analysis of scleraxis and Alcian blue staining of whole mount limb buds. RESULTS Compound related hindlimb defects were not restricted to a specific set of skeletal elements but consisted of a range of temporally related limb anomalies. Modest defects of the radius were observed as well. These results are consistent with a general insult to the limb mesenchyme. Mesenchymal cell death and reduced cell proliferation were also observed in both sets of limbs. The timing and location of these effects indicate a role for cytotoxicity in the etiology of dAZA induced limb defects. These effects also agree with the greater teratogenicity of dAZA in the hindlimb because they were more pronounced in that limb. The expression of scleraxis, a marker of early chondrogenesis, was reduced 12 hr after dAZA exposure, a time coincident with maximal cell death, as was the subsequent emergence of Alcian blue stained long bone anlagen. CONCLUSIONS These findings support the hypothesis that cytotoxic changes in the limb bud mesenchyme during early limb outgrowth can induce the proximal limb truncations characteristic of phocomelia after dAZA administration.
5-Aza-2'-脱氧胞苷诱导小鼠细胞毒性和肢体缺损。
背景5- aza -2'-脱氧胞苷(dAZA)引起CD-1小鼠后肢光秃。我们实验室的研究检验了化合物诱导的基因表达变化可能独特地影响后肢图案形成的假设。本研究验证了dAZA通过在肢体芽间质快速增殖的细胞中诱导细胞毒性导致肢体发育不良的假设。方法在妊娠第10天给予妊娠CD-1小鼠不同时间的致畸剂量dAZA,并采用标准方法评估胎儿两组肢体的骨骼发育情况。利用一般组织学和BrdU免疫组织化学,在给药后的不同时间,在最初的肢体芽生长后不久,评估胚胎的肢体间充质细胞死亡和细胞增殖。采用全坐骨肢芽的阿利新蓝染色和巩膜北分析,研究dAZA对早期肢体软骨形成的影响。结果复合相关后肢缺陷不局限于特定的一组骨骼元素,而是由一系列与时间相关的肢体异常组成。桡骨的中度缺损也被观察到。这些结果与肢体间质的普遍损伤一致。两组肢体均可见间充质细胞死亡和细胞增殖减少。这些作用的时间和位置表明细胞毒性在dAZA诱导的肢体缺陷病因学中的作用。这些效应也与dAZA在后肢更大的致畸性一致,因为它们在后肢更明显。在dAZA暴露12小时后,早期软骨形成的标志——硬化的表达减少,这一时间与最大的细胞死亡时间一致,随后出现阿利新蓝染色的长骨胶原。结论本研究结果支持了一种假说,即dAZA给药后,早期肢体生长过程中肢体芽间质的细胞毒性改变可引起光秃的近端截短。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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