Bioinformatics Unit.
Genomic Medicine Department, GENYO, Centre for Genomics and Oncological Research, Pfizer/University of Granada/Andalusian Regional Government, PTS 18016, Granada, Spain.
Bioinformatics. 2017 Dec 1;33(23):3691-3695. doi: 10.1093/bioinformatics/btx502.
Plasmacytoid dendritic cells (pDC) play a major role in the regulation of adaptive and innate immunity. Human pDC are difficult to isolate from peripheral blood and do not survive in culture making the study of their biology challenging. Recently, two leukemic counterparts of pDC, CAL-1 and GEN2.2, have been proposed as representative models of human pDC. Nevertheless, their relationship with pDC has been established only by means of particular functional and phenotypic similarities. With the aim of characterizing GEN2.2 and CAL-1 in the context of the main circulating immune cell populations we have performed microarray gene expression profiling of GEN2.2 and carried out an integrated analysis using publicly available gene expression datasets of CAL-1 and the main circulating primary leukocyte lineages.
Our results show that GEN2.2 and CAL-1 share common gene expression programs with primary pDC, clustering apart from the rest of circulating hematopoietic lineages. We have also identified common differentially expressed genes that can be relevant in pDC biology. In addition, we have revealed the common and differential pathways activated in primary pDC and cell lines upon CpG stimulatio.
R code and data are available in the supplementary material.
pedro.carmona@genyo.es or concepcion.maranon@genyo.es.
Supplementary data are available at Bioinformatics online.
浆细胞样树突状细胞(pDC)在调节适应性和先天免疫方面发挥着重要作用。人 pDC 难以从外周血中分离出来,并且在培养中不能存活,这使得对其生物学的研究具有挑战性。最近,两种白血病 pDC 的对应物,CAL-1 和 GEN2.2,被提议作为人 pDC 的代表性模型。然而,它们与 pDC 的关系仅通过特定的功能和表型相似性来建立。为了在主要循环免疫细胞群体的背景下表征 GEN2.2 和 CAL-1,我们对 GEN2.2 进行了微阵列基因表达谱分析,并使用 CAL-1 和主要循环原代白细胞谱系的公开可用基因表达数据集进行了综合分析。
我们的结果表明,GEN2.2 和 CAL-1 与原代 pDC 共享共同的基因表达程序,与其他循环造血谱系聚类分开。我们还鉴定了在 pDC 生物学中可能相关的常见差异表达基因。此外,我们揭示了在 CpG 刺激下原代 pDC 和细胞系中激活的常见和差异途径。
R 代码和数据可在补充材料中获得。
pedro.carmona@genyo.es 或 concepcion.maranon@genyo.es。
补充数据可在生物信息学在线获得。