Mournetas Virginie, Nunes Quentin M, Murray Patricia A, Sanderson Christopher M, Fernig David G
Department of Cellular and Molecular Physiology, Institute of Translational Medicine, University of Liverpool , Liverpool , United Kingdom ; Department of Biochemistry, Institute of Integrative Biology, University of Liverpool , Liverpool , United Kingdom.
Department of Biochemistry, Institute of Integrative Biology, University of Liverpool , Liverpool , United Kingdom ; NIHR Liverpool Pancreas Biomedical Research Unit, Institute of Translational Medicine, University of Liverpool , Liverpool , United Kingdom.
PeerJ. 2014 Oct 23;2:e618. doi: 10.7717/peerj.618. eCollection 2014.
Background. Human embryonic stem cells (hESCs) are pluripotent cells derived from the inner cell mass of in vitro fertilised blastocysts, which can either be maintained in an undifferentiated state or committed into lineages under determined culture conditions. These cells offer great potential for regenerative medicine, but at present, little is known about the mechanisms that regulate hESC stemness; in particular, the role of cell-cell and cell-extracellular matrix interactions remain relatively unexplored. Methods and Results. In this study we have performed an in silico analysis of cell-microenvironment interactions to identify novel proteins that may be responsible for the maintenance of hESC stemness. A hESC transcriptome of 8,934 mRNAs was assembled using a meta-analysis approach combining the analysis of microarrays and the use of databases for annotation. The STRING database was utilised to construct a protein-protein interaction network focused on extracellular and transcription factor components contained within the assembled transcriptome. This interactome was structurally studied and filtered to identify a short list of 92 candidate proteins, which may regulate hESC stemness. Conclusion. We hypothesise that this list of proteins, either connecting extracellular components with transcriptional networks, or with hub or bottleneck properties, may contain proteins likely to be involved in determining stemness.
背景。人类胚胎干细胞(hESCs)是源自体外受精囊胚内细胞团的多能细胞,其既可以维持未分化状态,也可以在特定培养条件下分化为特定谱系。这些细胞为再生医学提供了巨大潜力,但目前对于调控hESC干性的机制了解甚少;特别是细胞间和细胞与细胞外基质相互作用的作用仍相对未被探索。方法与结果。在本研究中,我们对细胞 - 微环境相互作用进行了计算机分析,以鉴定可能负责维持hESC干性的新蛋白。使用元分析方法,结合微阵列分析和注释数据库,组装了一个包含8934个mRNA的hESC转录组。利用STRING数据库构建了一个蛋白质 - 蛋白质相互作用网络,该网络聚焦于组装转录组中包含的细胞外和转录因子成分。对这个相互作用组进行了结构研究和筛选,以确定92个可能调控hESC干性的候选蛋白的简短列表。结论。我们假设,这个蛋白质列表,无论是将细胞外成分与转录网络连接起来,还是具有枢纽或瓶颈特性,可能包含可能参与决定干性的蛋白质。