We have characterized gene expression changes in HeLa cells following long term depletion of Cyclin T2 or Cyclin T1 using shRNA
Limited redundancy in genes regulated by Cyclin T2 and Cyclin T1.
Cell line, Treatment
View SamplesTo investigate the detailed molecular mechanisms for the regulatory role of HIF-1 in colon, microarray gene expression analysis was performed on colon RNA isolated from 6- to 8-week-old Hif-1+/+, Hif-1LSL/LSL mice.
Activation of HIF-1α does not increase intestinal tumorigenesis.
Age, Specimen part
View SamplesThis SuperSeries is composed of the SubSeries listed below.
Cyclin T1-dependent genes in activated CD4 T and macrophage cell lines appear enriched in HIV-1 co-factors.
No sample metadata fields
View SamplesParental MM6 cells, as an additional control, were treated with LPS and PMA. Genes affected by the treatments were identified.
Cyclin T1-dependent genes in activated CD4 T and macrophage cell lines appear enriched in HIV-1 co-factors.
No sample metadata fields
View SamplesCyclin T1-dependent genes in PMA-activated MM6 cells.
Cyclin T1-dependent genes in activated CD4 T and macrophage cell lines appear enriched in HIV-1 co-factors.
No sample metadata fields
View SamplesCyclin T1-dependent genes in LPS-activated MM6 cells.
Cyclin T1-dependent genes in activated CD4 T and macrophage cell lines appear enriched in HIV-1 co-factors.
No sample metadata fields
View SamplesCyclin T1-dependent genes in activated Jurkat cells.
Cyclin T1-dependent genes in activated CD4 T and macrophage cell lines appear enriched in HIV-1 co-factors.
No sample metadata fields
View SamplesCyclin T1-dependent genes in non-activated Jurkat cells.
Cyclin T1-dependent genes in activated CD4 T and macrophage cell lines appear enriched in HIV-1 co-factors.
No sample metadata fields
View SamplesCyclin T1-dependent genes in LPS-activated MM6 cells.
Cyclin T1-dependent genes in activated CD4 T and macrophage cell lines appear enriched in HIV-1 co-factors.
No sample metadata fields
View SamplesIron is essential for many cellular processes and is required by bacteria for replication. To acquire iron from the host, pathogenic Gram-negative bacteria secrete siderophores, including Enterobactin (Ent). However, Ent is bound by the host protein Lipocalin 2 (Lcn2), preventing bacterial reuptake of aferric or ferric Ent. In two experiments we treated A549 (lung cancer cell line) cells with Lcn2, Ent, and iron, alone and in combination. In experiment 1, biological duplicates of 4 conditions were used: PBS control, Lcn2, Lcn2+Ent, and Lcn2+Ent+iron. In experiment 2, 4 biological replicates of 4 conditions were used: PBS control, Ent, iron, and Ent+iron. Targets made from the samples were hybridized to Affymetrix Human Gene 1.0 ST arrays to measure transcript abundances. The RMA algorithm was used to estimate transcript levels. Replicate samples were exchangeable, so we fit one-way ANOVA models to log2-transformed data separately to each experiment, and tested for pairwise differences between groups in each experiment, as well as asking if the Ent vs. PBS differences were larger or smaller than the Ent+iron vs. iron differences (Ent by iron interactions). We report results for 29096 probe-sets that were not annotated as positive or negative controls on the array. A supplementary Excel workbook is provided that contains the estimated expression level, some probe-set annotation, and simple statistical analysis for each probe-set. It may be convenient for some users, however obtaining newer probe-set annotation may be advisable.
Bacterial siderophores that evade or overwhelm lipocalin 2 induce hypoxia inducible factor 1α and proinflammatory cytokine secretion in cultured respiratory epithelial cells.
Specimen part, Cell line
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