Department of Neuroregeneration, Netherlands Institute for Neuroscience, Meibergdreef 47, Amsterdam, The Netherlands.
Exp Neurol. 2011 May;229(1):10-45. doi: 10.1016/j.expneurol.2011.03.001. Epub 2011 Mar 23.
Genome wide transcriptional profiling and large scale proteomics have emerged as two powerful methods to dissect the molecular properties of specific neural tissues or cell types on a global scale. Several genome-wide transcriptional profiling and proteomics studies have been published on cultured olfactory ensheathing cells (OEC). In this article we present a meta-analysis of all five published and publicly available micro-array gene expression datasets of cultured early-passage-OB-OEC with other cell types (Schwann cells, late-passage-OB-OEC, mucosa-OEC, an OEC cell line, and acutely dissected OEC). The aim of this meta-analysis is to identify genes and molecular pathways that are found in multiple instead of one isolated study. 454 Genes were detected in at least three out of five microarray datasets. In this "Top-list", genes involved in the biological processes "growth of neurites", "blood vessel development", "migration of cells" and "immune response" were strongly overrepresented. By applying network analysis tools, molecular networks were constructed and Hub-genes were identified that may function as key genes in the above mentioned interrelated processes. We also identified 7 genes (ENTPD2, MATN2, CTSC, PTHLH, GLRX1, COL27A1 and ID2) with uniformly higher or lower expression in early-passage-OB-OEC in all five microarray comparisons. These genes have diverse but intriguing roles in neuroprotection, neurite extension and/or tissue repair. Our meta-analysis provides novel insights into the molecular basis of OB-OEC-mediated neural repair and can serve as a repository for investigators interested in the molecular biology of OEC. This article is part of a Special Issue entitled: Understanding olfactory ensheathing glia and their prospect for nervous system repair.
全基因组转录谱分析和大规模蛋白质组学已经成为两种强大的方法,可以在全球范围内剖析特定神经组织或细胞类型的分子特性。已经有几项关于培养嗅鞘细胞(OEC)的全基因组转录谱分析和蛋白质组学研究发表。在本文中,我们对所有已发表和公开的培养早期传代-嗅球-OEC 与其他细胞类型(施万细胞、晚期传代-嗅球-OEC、黏膜-OEC、OEC 细胞系和急性分离的 OEC)的五个微阵列基因表达数据集进行了荟萃分析。本荟萃分析的目的是确定在多个而不是一个孤立的研究中发现的基因和分子途径。在至少五个微阵列数据集的三个或三个以上中检测到 454 个基因。在这个“顶级列表”中,参与“神经突生长”、“血管发育”、“细胞迁移”和“免疫反应”等生物学过程的基因强烈过表达。通过应用网络分析工具,构建了分子网络,并鉴定了可能作为上述相互关联过程中关键基因的 Hub 基因。我们还鉴定了 7 个基因(ENTPD2、MATN2、CTSC、PTHLH、GLRX1、COL27A1 和 ID2)在所有五个微阵列比较中在早期传代-嗅球-OEC 中的表达水平均较高或较低。这些基因在神经保护、神经突延伸和/或组织修复方面具有多样化但有趣的作用。我们的荟萃分析为 OB-OEC 介导的神经修复的分子基础提供了新的见解,并可为对 OEC 分子生物学感兴趣的研究人员提供信息库。本文是一个特刊的一部分,标题为:理解嗅鞘胶质细胞及其对神经系统修复的前景。