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支持树突状细胞发育的基质细胞的基因特征。

Gene signature of stromal cells which support dendritic cell development.

作者信息

Despars Geneviève, Periasamy Pravin, Tan Jonathan, Abbey Janice, O'Neill Terence J, O'Neill Helen C

机构信息

School of Biochemistry and Molecular Biology, The Australian National University, Canberra, ACT, Australia.

出版信息

Stem Cells Dev. 2008 Oct;17(5):917-27. doi: 10.1089/scd.2007.0170.

Abstract

Spleen stromal cells are critical determinants of dendritic cell (DC) development in spleen. The spleen stromal line, namely STX3, supports DC differentiation in vitro from overlaid bone marrow cells while the lymph node stromal line, namely 2RL22, does not. Here we have characterised the hematopoietic support capacity of each stroma, and analysed lineage origin of the stromal cell lines by gene profiling using microarrays. Stromal co-culture experiments were performed using bone marrow cells as a source of hematopoietic progenitors. A characteristic immature myeloid-like CD11c(+)CD11b(+)CD86(+)MHC-II(/lo)B220()CD8alpha() DC is produced after 14 days in STX3 cocultures, while 2RL22 cocultures produce only monocyte/macrophage-like cells. No other hematopoietic cell type is produced. The STX3 and 2RL22 stroma were compared by transcriptome analysis utilising Affymetrix Murine U74Av2 genechips to identify gene expression related to differential hematopoietic support function. Data mining was used to determine cell surface marker expression reflecting endothelial cells and fibroblasts, as well as adhesion molecules contributing to the microenvironment. STX3 shows gene expression reflective of early endothelial cells, while 2RL22 expresses markers specific to fibroblasts. The expression of genes like Flt1, CD34, Mcam, and Eng distinguishes STX3 as an early immature endothelial cell lacking markers of angioblasts or hemangioblasts like Tal1/SCL, Tie1, Tie2, Kdr or Prom1/AC133. The absence of expression of genes like Vwf and Cd31 distinguishes STX3 from fully differentiated vascular endothelial cells. In contrast, the 2RL22 lymph node stroma specifically expresses genes related to fibroblastic-like cells like osteoblasts with expression of Vdr (Vitamin D receptor), and epithelial cells with expression of Krt13 (keratins). Gene expression data identifies STX3 as splenic endothelial cells, independently able to support the outgrowth of immature, myeloid DC-like cells from progenitors present in bone marrow, while 2RL22 lymph node fibroblastic cells provide support for development of monocytes/macrophages.

摘要

脾基质细胞是脾脏中树突状细胞(DC)发育的关键决定因素。脾基质系,即STX3,能在体外支持覆盖的骨髓细胞分化为DC,而淋巴结基质系,即2RL22,则不能。在此,我们已对每种基质的造血支持能力进行了表征,并通过使用微阵列的基因谱分析来分析基质细胞系的谱系起源。使用骨髓细胞作为造血祖细胞来源进行基质共培养实验。在STX3共培养14天后会产生一种特征性的未成熟髓样CD11c(+)CD11b(+)CD86(+)MHC-II(/lo)B220()CD8alpha() DC,而2RL22共培养仅产生单核细胞/巨噬样细胞。未产生其他造血细胞类型。利用Affymetrix鼠U74Av2基因芯片通过转录组分析对STX3和2RL22基质进行比较,以鉴定与不同造血支持功能相关的基因表达。数据挖掘用于确定反映内皮细胞和成纤维细胞的细胞表面标志物表达,以及对微环境有贡献的黏附分子。STX3显示出反映早期内皮细胞的基因表达,而2RL22表达成纤维细胞特有的标志物。Flt1、CD34、Mcam和Eng等基因的表达将STX3区分成为缺乏成血管细胞或造血干细胞标志物(如Tal1/SCL、Tie1、Tie2、Kdr或Prom1/AC133)的早期未成熟内皮细胞。Vwf和Cd31等基因表达的缺失将STX3与完全分化的血管内皮细胞区分开来。相比之下,2RL22淋巴结基质特异性表达与成纤维样细胞相关的基因,如表达Vdr(维生素D受体)的成骨细胞,以及表达Krt13(角蛋白)的上皮细胞。基因表达数据将STX3鉴定为脾内皮细胞,其能够独立支持骨髓中祖细胞产生未成熟的髓样DC样细胞的生长,而2RL22淋巴结成纤维细胞则为单核细胞/巨噬细胞的发育提供支持。

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