Myeloid Derived Suppressor Cells and Cancer. Mus musculus
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https://www.ncbi.nlm.nih.gov/bioproject/PRJNA135049
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Transcriptional profiling of FACS-sorted and splenic control mouse cells, comparing splenic cells from FVBneuN vs Neu+ expressing FVBneuN mice with Gr1+ CD11b+ sorted tumor-infiltrating mononuclear or splenic myeloid-derived suppressor cells Overall design: 4 groups or conditions. Biological replicates: 2 or 3 per condition. One replicate array per sample. manuscript: van Deventer, H, J Burgents, QP Wu, R Woodford, WJ Brickey, I Allen, E McElvania-Tekippe, J Serody, and J Ting. (2010) The inflammasome component Nlrp3 impairs antitumor vaccine by enhancing the accumulation of tumor-associated myeloid-derived suppressor cells. Cancer Research. variable: cell type: splenic cells from normal FVB-neuN mice, splenic cells from Neu+ tumor-bearing FVB-neuN mice, Gr1+ CD11b+ sorted cells from tumor, Gr1+ CD11b+ sorted cells from spleen repear: biological replicate: #1, #2, #3
本数据集针对经荧光激活细胞分选(Fluorescence-Activated Cell Sorting, FACS)分选的细胞及脾脏对照小鼠细胞开展转录组谱分析,对比分析FVBneuN小鼠脾脏细胞、表达Neu+的FVBneuN小鼠脾脏细胞,以及经Gr1+ CD11b+分选的肿瘤浸润单核细胞或脾脏髓系来源抑制细胞(myeloid-derived suppressor cells, MDSC)。实验设计:共设置4组实验条件,每组生物学重复数为2或3,每个样本对应一张基因芯片(array)。相关研究参考文献:van Deventer H、Burgents J、Wu QP、Woodford R、Brickey WJ、Allen I、McElvania-Tekippe E、Serody J与Ting J于2010年发表于《Cancer Research》的论文,原英文标题为"The inflammasome component Nlrp3 impairs antitumor vaccine by enhancing the accumulation of tumor-associated myeloid-derived suppressor cells",中文译名为《炎症小体(inflammasome)组分Nlrp3通过促进肿瘤相关髓系来源抑制细胞积累削弱抗肿瘤疫苗功效》。实验变量为细胞类型,具体包含以下四类:正常FVB-neuN小鼠脾脏细胞、携带Neu+肿瘤的FVB-neuN小鼠脾脏细胞、肿瘤来源的Gr1+ CD11b+分选细胞、脾脏来源的Gr1+ CD11b+分选细胞。实验重复信息:采用生物学重复,重复编号为#1、#2、#3。
创建时间:
2010-12-29



