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Links from GEO DataSets

Items: 10

1.

1,25-Dihydroxyvitamin D Promotes Negative Feedback Regulation of Toll-Like Receptor Signaling via Targeting MicroRNA-155-SOCS1 in Macrophages

(Submitter supplied) The negative feedback mechanism is essential to maintain effective immunity and tissue homeostasis. 1,25-dihydroxyvitamin D (1,25(OH)2D3) modulates innate immune response, but the mechanism remains poorly understood. Here we report that vitamin D receptor (VDR) signaling attenuates Toll-like receptor-mediated inflammation by enhancing the negative feedback inhibition. VDR inactivation leads to a hyperinflammatory response in mice and macrophage cultures when challenged with lipopolysaccharide (LPS) due to miR-155 overproduction that excessively suppresses SOCS1, a key regulator that enhances the negative feedback loop. more...
Organism:
Murid gammaherpesvirus 4; Betapolyomavirus hominis; Mus musculus; Rattus norvegicus; Murid betaherpesvirus 1; JC polyomavirus; Human immunodeficiency virus 1; Human gammaherpesvirus 8; Homo sapiens; Human alphaherpesvirus 1; Human betaherpesvirus 5; human gammaherpesvirus 4; Betapolyomavirus macacae
Type:
Non-coding RNA profiling by array
Platform:
GPL7723
6 Samples
Download data: GPR
Series
Accession:
GSE43300
ID:
200043300
2.

IFNgamma and 1a,25(OH)2D3 dependent gene expression in bone marrow derived macrophages

(Submitter supplied) Gene expression profiling of macrophages derived from WT and Vdr deficient mice after stimulation with IFNgamma and/or 1alpha,25(OH)2D3 Keywords = macrophages Keywords = VDR Keywords = activated vitamin D3 Keywords = IFNgamma Keywords = KO mice Keywords: dose response
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS1389
Platform:
GPL339
8 Samples
Download data: CEL, CHP, RPT
Series
Accession:
GSE2421
ID:
200002421
3.
Full record GDS1389

1alpha,25-dihydroxyvitamin D3 suppressive effect on IFN-gamma activated macrophages

Analysis of wild type and vitamin D receptor (Vdr) knockout primary bone marrow-derived macrophages following treatment with IFN-gamma and/or 1alpha,25-dihydroxyvitamin D3 (1alpha,25(OH)2D3). Results indicate that 1alpha,25(OH)2D3 suppresses effector functions of IFN-gamma-activated macrophages.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 4 agent, 2 genotype/variation sets
Platform:
GPL339
Series:
GSE2421
8 Samples
Download data: CEL, CHP, RPT
DataSet
Accession:
GDS1389
ID:
1389
4.

RNA Sequencing Analysis of Mouse Bone Marrow Derived Dendritic Cells Transcriptomes During Maturation

(Submitter supplied) Purpose:The purpose of this study is to detect activated or silenced genes during LPS-induced dendritic cell maturation. Gene expression differences between two samples could be found using transcriptome profiling (RNA-seq) analysis. Methods:Mouse dendritic cells were generated from bone marrow cells in RPMI-1640 medium with recombinant mouse GM-CSF and IL-4, mature DCs were obtained after LPS induced maturation. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
2 Samples
Download data: TXT
Series
Accession:
GSE60307
ID:
200060307
5.

Vitamin D treatment timing is critical for transcriptome modulation of immune challenged primary human cells

(Submitter supplied) In this study, the transcriptome of peripheral blood mononuclear cells (PBMCs) of a healthy adult was investigated in response to in vitro treatment with LPS, beta-glucan and 1,25(OH)2D3.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
54 Samples
Download data: XLSX
6.

Time-Resolved Gene Expression Analysis Monitors the Regulation of Inflammatory Mediators and Attenuation of Adaptive Immune Response by Vitamin D

(Submitter supplied) In this study, we focused on the time-course of transcriptional changes in freshly isolated human PBMCs 4, 8, 24 and 48 h after onset of stimulation with the active vitamin D metabolite 1α,25-dihydroxyvitamin D3 (1,25(OH)2D3) compared to vehicle (0.1% EtOH).
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
24 Samples
Download data: XLSX
7.

Regulation of miRNAs in macrophages in response to Candida albacans

(Submitter supplied) In this study we have analysed the regulation of miRNA in bone marrow derived macrophages in response to the fungal pathogen heat killed Candida albicans and bacterial cell wall component, LPS. The aim of the study was to identify and validate miRNAs involved in the innate immune system in response to fungal and bacterial stimuli and investigate potential mechanisms for their transcription.
Organism:
Mus musculus
Type:
Non-coding RNA profiling by array
Platform:
GPL10458
5 Samples
Download data: XLS
Series
Accession:
GSE21970
ID:
200021970
8.

Macrophage Secretion of miR-106b-5p Causes Renin-Dependent Hypertension

(Submitter supplied) We generated myeloid cells lacking VDR (KODMAC) by crossing Vdrfl/fl mice with lysosome-M-promoter-driven Cre mice (Lyz2Cre) in the Ldlr-/-background (a model of diet-induced metabolic syndrome), as previously described13 and compared them to Vdrfl/flLdlr-/- littermates (control). Unbiased miRNA expression analyses using media from KODMAC or control peritoneal macrophages identified 361 differentially expressed miRNAs with p<0.05
Organism:
Mus musculus; synthetic construct
Type:
Non-coding RNA profiling by array
Platform:
GPL19117
18 Samples
Download data: CEL
Series
Accession:
GSE155511
ID:
200155511
9.

mRNA- and RISC-sequencing of miR-106b-transfected juxtaglomerular (JG) cells

(Submitter supplied) Chronic inflammation is known to contribute to the development of hypertension, but while the role of lymphocytes is well-established, the myeloid lineage, particularly as a possible mediator of renin-mediated hypertension, has not been studied. Vitamin D deficiency has pro-inflammatory consequences in monocytes, and it is linked to renin-mediated hypertension in mice. This prompted us to test the hypothesis that conditional knockout of the vitamin D receptor (VDR) in macrophages (KODMAC) would promote renin-dependent hypertension. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
16 Samples
Download data: TXT
Series
Accession:
GSE117704
ID:
200117704
10.

A novel CRISPR/Cas9 screening platform identifies an IRF1-SOCS1-mediated negative feedback loop that limits CXCL9 expression and anti-tumor immunity

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus; Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Other
Platforms:
GPL18573 GPL19057
56 Samples
Download data: NARROWPEAK
Series
Accession:
GSE237974
ID:
200237974
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