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经 PBEFsiRNA 处理的人肺微血管内皮细胞转录组学揭示了前 B 细胞集落增强因子 (PBEF) 的多效性功能。

Pleiotropic functions of pre-B-cell colony-enhancing factor (PBEF) revealed by transcriptomics of human pulmonary microvascular endothelial cells treated with PBEFsiRNA.

机构信息

Department of Pediatrics, Children's Mercy Hospitals and Clinics, University of Missouri School of Medicine, Kansas City, MO 64108, USA.

出版信息

Genes Cells. 2012 May;17(5):420-30. doi: 10.1111/j.1365-2443.2012.01598.x. Epub 2012 Apr 9.

Abstract

This study profiled transcriptomes of human pulmonary microvascular endothelial cells (HMVEC-L) treated with pre-B-cell colony-enhancing factor (PBEF) siRNA or scrambled RNA to gain insight into transcriptional regulations of PBEF on the endothelial function using the Affymetrix GeneChips HG-U133 plus 2. Several important themes are emerged from this study. First, PBEF affected expressions of multiple genes in the endothelium. Expression of 373 genes was increased and 64 genes decreased by at least 1.3-fold in the PBEFsiRNA-treated HMVEC-L versus the scramble RNA control. Second, the microarray results confirmed previous reports of PBEF-mediated gene expressions in some pathways but provided a more complete repertoire of molecules in those pathways. Third, most of the affected canonical pathways have not previously been reported to be PBEF responsive. Fourth, network analysis supports that PBEF has pleiotropic functions. Our first transcriptome analysis of human pulmonary microvascular endothelial cells treated with PBEFsiRNA has provided important insights into the transcriptional regulation of gene expression in HMVEC-L cells by PBEF. Further in-depth analysis of these transcriptional regulations may shed light on molecular mechanisms underlying PBEF-mediated endothelial functions and dysfunctions in various diseases and provide new leads of therapeutic targets to those diseases.

摘要

本研究利用 Affymetrix GeneChips HG-U133 plus 2 对经 pre-B 细胞集落增强因子 (PBEF) siRNA 或乱序 RNA 处理的人肺微血管内皮细胞 (HMVEC-L) 的转录组进行了分析,旨在深入了解 PBEF 对内皮功能的转录调控。本研究中出现了几个重要主题。首先,PBEF 影响内皮细胞中多个基因的表达。与乱序 RNA 对照相比,PBEFsiRNA 处理的 HMVEC-L 中 373 个基因的表达增加,64 个基因的表达至少减少 1.3 倍。其次,微阵列结果证实了之前报道的 PBEF 介导的某些途径中的基因表达,但提供了这些途径中更完整的分子谱。第三,大多数受影响的经典途径以前没有报道过对 PBEF 有反应。第四,网络分析支持 PBEF 具有多种功能。我们首次对经 PBEFsiRNA 处理的人肺微血管内皮细胞进行了转录组分析,为 PBEF 对 HMVEC-L 细胞中基因表达的转录调控提供了重要见解。对这些转录调控的进一步深入分析可能揭示 PBEF 介导的内皮功能障碍和各种疾病中分子机制,并为这些疾病提供治疗靶点的新线索。

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