Marland G, Hartgers F C, Veltkamp R, Königswieser M F, Gorman D, McClanahan T, Figdor C G, Adema G J
Department of Tumor Immunology, University Hospital Nijmegen, The Netherlands.
Adv Exp Med Biol. 1997;417:443-8. doi: 10.1007/978-1-4757-9966-8_73.
To increase our understanding of dendritic cell (DC) function we have used two approaches to search at the genetic level for molecules which are specifically expressed by these cells. First, we have performed random sequencing of cDNA libraries prepared from DC. Second, we have employed differential display PCR (DD-PCR). DD-PCR is a powerful technique for the identification at the RNA level of molecules which are expressed in a cell type-specific manner. In our study, we have compared RNA from DC with RNA from a panel of leukocyte cell lines. Here we present a summary of our findings using these two approaches, and show that both methods are complementary and can be used to identify molecules that are specific to DC.
为了增进我们对树突状细胞(DC)功能的理解,我们采用了两种方法在基因水平上寻找这些细胞特异性表达的分子。第一,我们对从DC制备的cDNA文库进行了随机测序。第二,我们采用了差异显示PCR(DD-PCR)。DD-PCR是一种强大的技术,可在RNA水平上鉴定以细胞类型特异性方式表达的分子。在我们的研究中,我们将DC的RNA与一组白细胞细胞系的RNA进行了比较。在此,我们总结了使用这两种方法的研究结果,并表明这两种方法是互补的,可用于鉴定DC特有的分子。