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乙醇暴露会改变胎儿酒精谱系障碍小鼠模型中的蛋白质表达。

Ethanol exposure alters protein expression in a mouse model of fetal alcohol spectrum disorders.

作者信息

Mason Stephen, Anthony Bruce, Lai Xianyin, Ringham Heather N, Wang Mu, Witzmann Frank A, You Jin-Sam, Zhou Feng C

机构信息

Department of Anatomy and Cell Biology, Indiana University School of Medicine, Indianapolis, IN 46202, USA.

出版信息

Int J Proteomics. 2012;2012:867141. doi: 10.1155/2012/867141. Epub 2012 Jun 14.

Abstract

Alcohol exposure during development can result in variable growth retardation and facial dysmorphology known as fetal alcohol spectrum disorders. Although the mechanisms underlying the disorder are not fully understood, recent progress has been made that alcohol induces aberrant changes in gene expression and in the epigenome of embryos. To inform the gene and epigenetic changes in alcohol-induced teratology, we used whole-embryo culture to identify the alcohol-signature protein profile of neurulating C6 mice. Alcohol-treated and control cultures were homogenized, isoelectrically focused, and loaded for 2D gel electrophoresis. Stained gels were cross matched with analytical software. We identified 40 differentially expressed protein spots (P < 0.01), and 9 spots were selected for LC/MS-MS identification. Misregulated proteins include serotransferrin, triosephosphate isomerase and ubiquitin-conjugating enzyme E2 N. Misregulation of serotransferrin and triosephosphate isomerase was confirmed with immunologic analysis. Alteration of proteins with roles in cellular function, cell cycle, and the ubiquitin-proteasome pathway was induced by alcohol. Several misregulated proteins interact with effectors of the NF-κB and Myc transcription factor cascades. Using a whole-embryo culture, we have identified misregulated proteins known to be involved in nervous system development and function.

摘要

发育过程中接触酒精会导致生长发育迟缓以及面部畸形,即胎儿酒精谱系障碍。尽管该病症的潜在机制尚未完全明确,但近期研究取得了进展,即酒精会引发胚胎基因表达和表观基因组的异常变化。为了了解酒精诱导的致畸学中的基因和表观遗传变化,我们利用全胚胎培养来鉴定神经管形成期C6小鼠的酒精特征蛋白谱。将经酒精处理的培养物和对照培养物匀浆、等电聚焦,然后进行二维凝胶电泳。对染色后的凝胶使用分析软件进行交叉比对。我们鉴定出40个差异表达的蛋白点(P < 0.01),并选择了9个点进行液相色谱-质谱联用(LC/MS-MS)鉴定。失调的蛋白质包括血清转铁蛋白、磷酸丙糖异构酶和泛素结合酶E2 N。通过免疫分析证实了血清转铁蛋白和磷酸丙糖异构酶的失调。酒精诱导了在细胞功能、细胞周期和泛素-蛋白酶体途径中起作用的蛋白质的改变。几种失调的蛋白质与核因子-κB(NF-κB)和Myc转录因子级联反应的效应器相互作用。通过全胚胎培养,我们鉴定出了已知参与神经系统发育和功能的失调蛋白质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8cc/3382221/f48203571fa8/IJPRO2012-867141.001.jpg

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