Lee Philip R, Cohen Jonathan E, Tendi Elisabetta A, Farrer Robert, DE Vries George H, Becker Kevin G, Fields R Douglas
Section on Nervous System Development and Plasticity, Bldg. 35, Rm. 2A211, MSC 3713 NICHD, National Institutes of Health, Bethesda, MD 20892, USA.
Neuron Glia Biol. 2004 May;1(2):135-47. doi: 10.1017/s1740925x04000274.
cDNA microarrays were utilized to identify abnormally expressed genes in a malignant peripheral nerve sheath tumor (MPNST)-derived cell line, T265, by comparing the mRNA abundance profiles with that of normal human Schwann cells (nhSCs). The findings characterize the molecular phenotype of this important cell-line model of MPNSTs, and elucidate the contribution of Schwann cells in MPNSTs. In total, 4608 cDNA sequences were screened and hybridizations replicated on custom cDNA microarrays. In order to verify the microarray data, a large selection of differentially expressed mRNA transcripts were subjected to semi-quantitative reverse transcription PCR (LightCycler). Western blotting was performed to investigate a selection of genes and signal transduction pathways, as a further validation of the microarray data. The data generated from multiple microarray screens, semi-quantitative RT-PCR and Western blotting are in broad agreement. This study represents a comprehensive gene-expression analysis of an MPNST-derived cell line and the first comprehensive global mRNA profile of nhSCs in culture. This study has identified ~900 genes that are expressed abnormally in the T265 cell line and detected many genes not previously reported to be expressed in nhSCs. The results provide crucial information on the T265 cells that is essential for investigation using this cell line in experimental studies in neurofibromatosis type I (NF1), and important information on normal human Schwann cells that is applicable to a wide range of studies on Schwann cells in cell culture.
通过将恶性外周神经鞘瘤(MPNST)来源的细胞系T265的mRNA丰度谱与正常人雪旺细胞(nhSCs)的进行比较,利用cDNA微阵列来鉴定异常表达的基因。这些发现描绘了MPNST这一重要细胞系模型的分子表型,并阐明了雪旺细胞在MPNST中的作用。总共筛选了4608个cDNA序列,并在定制的cDNA微阵列上重复进行杂交。为了验证微阵列数据,对大量差异表达的mRNA转录本进行了半定量逆转录PCR(LightCycler)。进行蛋白质印迹分析以研究一系列基因和信号转导途径,作为对微阵列数据的进一步验证。多个微阵列筛选、半定量RT-PCR和蛋白质印迹产生的数据基本一致。本研究代表了对MPNST来源的细胞系进行的全面基因表达分析,以及首次对培养中的nhSCs进行的全面全球mRNA谱分析。本研究鉴定出约900个在T265细胞系中异常表达的基因,并检测到许多以前未报道在nhSCs中表达的基因。这些结果提供了关于T265细胞的关键信息,这对于在I型神经纤维瘤病(NF1)的实验研究中使用该细胞系至关重要,同时也提供了关于正常人雪旺细胞的重要信息,适用于细胞培养中关于雪旺细胞的广泛研究。