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Links from GEO DataSets

Items: 20

1.

Immune Response to Nippostrongylus brasiliensis in the mouse lung

(Submitter supplied) The goal of this experiment was to examine the innate immune response to helminth infection in the lung. Hookworms (like many other helminths) use an obligate migration pathway through the lung. Their infection has been characterized in the gut in detail, but early immune responses in the lung have not been fully characterized. Keywords: Time Course
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2024
Platform:
GPL1261
36 Samples
Download data: CEL
Series
Accession:
GSE3414
ID:
200003414
2.
Full record GDS2024

Lung immune response to Nippostrongylus brasiliensis infection: time course

Analysis of lungs of SCID animals at various time points up to 12 days post infection with Nippostrongylus brasiliensis. SCID animals have no functional B or T cells but a fully functional innate immune system. Results provide insight into the immune response to helminth infection in the lung.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 infection, 2 strain, 6 time sets
Platform:
GPL1261
Series:
GSE3414
36 Samples
Download data: CEL
3.

Hookworm-Induced Persistent Changes to the Immunological Environment of the Lung

(Submitter supplied) Infection with Nippostrongylus brasiliensis results in persistent changes to the lung environment. Cytokine profiling reveals a sustained increase in both Th1 and Th2 transcripts. Cellular populations of macrophages display an alternative phenotype, with upregulation of YM1, Arg1, Mrc1 as well as Class II MHC. These alternatively activated alveolar macrophages (AAAMs) also increase drastically in number. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
42 Samples
Download data: CEL
Series
Accession:
GSE5555
ID:
200005555
4.

Analysis of tissue-derived alveolar and monocyte-derived alveolar macrophages at day 7 and day 14 post-nippostrongylus brasiliensis infection.

(Submitter supplied) Alveolar macrophages from Cx3cR1-CreER x Rosa26-tandem dimer Tomato(TdT) control and infected mice were sort-purified on live CD45+CD64+F4/80+CD11c+SiglecF+ and then sorted based on expression of TdT, with tissue-resident cells being TdT- and monocyte-derived cells TdT+. Illumina-compatible libraries were generated using the NEBNext Ultra II DNA Library Prep Kit for Illumina (catalog no. E7645S; New England BioLabs) and sequenced using an Illumina NextSeq 550 in a single-end 75-base pair (bp) read configuration. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
21 Samples
Download data: TXT
Series
Accession:
GSE189675
ID:
200189675
5.

Lung macrophages mediate helminth resistance through differential activation of recruited monocyte-derived alveolar macrophages and arginine depletion

(Submitter supplied) Lung macrophages mediate helminth resistance through differential activation of recruited monocyte-derived alveolar macrophages and arginine depletion
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24247
12 Samples
Download data: TXT
Series
Accession:
GSE189674
ID:
200189674
6.

RELMa induced differential gene expression in CD11c+ cells

(Submitter supplied) Mouse lung CD11c+ cell gene expression changes following recombinant RELMa treatment
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL25266
12 Samples
Download data: RCC, TXT
Series
Accession:
GSE116552
ID:
200116552
7.

Expression Data from BALB/c and Stat6-deficient bone marrow derived macrophages (BMDM)

(Submitter supplied) We used microarrays to find Stat6 dependent genes in control and IL-4 exposed bone marrow derived macrophages. Alternatively activated macrophages (AAM) accumulate in tissues during Th2-associated immune responses like helminth infections and allergic disorders. These cells possess potent inhibitory activity against T cells. The differentiation of AAM depends on IL-4/IL-13-mediated activation of the transcription factor Stat6. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
4 Samples
Download data: CEL, CHP
Series
Accession:
GSE20030
ID:
200020030
8.

Stat6 dependent gene expression in lung and small intestine

(Submitter supplied) Gene expression in the lung and intestine of wild-type and stat6 deficient mice on BALB/c background infected with the helminth parasite Nippostrongylus brasiliensis was compared by competitive hybridization to spotted 70-mer oligonucleotide arrays. Keywords: other
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL929
2 Samples
Download data
Series
Accession:
GSE2717
ID:
200002717
9.

Neutrophils promote M2 polarization of macrophages during Nippostrongylus brasiliensis infection

(Submitter supplied) Microarray profiling of amplified total RNA isolated from neutrophils sorted from naïve, Nippostrongylus brasiliensis (Nb)-infected, or lipopolysaccharide (LPS)-treated mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL13912
8 Samples
Download data: TXT
Series
Accession:
GSE46437
ID:
200046437
10.

Macrophage migration inhibitory factor (MIF) is essential for Type 2 effector cell immunity to an intestinal helminth parasite

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6887
47 Samples
Download data
Series
Accession:
GSE139009
ID:
200139009
11.

Intestinal tissues (duodenum) from wild-type (BALB/c) and MIF deficient mice were compared in the steady state and at two different time points (day 3 and day 7) following infection with the gastrointestinal helminth parasite Heligmosomoides polygyrus

(Submitter supplied) We have found that macrophage migration inhibitory factor (MIF) is essential for the development of effective immunity to the intestinal helminth Heligmosomoides polygyrus, even following vaccination which induces sterile immunity in wild-type mice. In the context of a Type 2 infection, MIF plays a critical role in polarizing macrophages into the protective alternatively-activated phenotype, and that STAT3 signaling may make a previously unrecognized contribution to immunity to helminths.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6887
24 Samples
Download data: TXT
Series
Accession:
GSE139008
ID:
200139008
12.

Duodenal tissues and mesenteric lymph nodes from wild-type (BALB/c) and MIF deficient mice were compared in the steady state and at day 5 following infection with the gastrointestinal helminth parasite Heligmosomoides polygyrus

(Submitter supplied) We have found that macrophage migration inhibitory factor (MIF) is essential for the development of effective immunity to the intestinal helminth Heligmosomoides polygyrus, even following vaccination which induces sterile immunity in wild-type mice. In the context of a Type 2 infection, MIF plays a critical role in polarizing macrophages into the protective alternatively-activated phenotype, and that STAT3 signaling may make a previously unrecognized contribution to immunity to helminths.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6887
23 Samples
Download data: TXT
Series
Accession:
GSE139007
ID:
200139007
13.

The lung environment controls alveolar macrophage metabolism and responsiveness during type-2 inflammation.

(Submitter supplied) Fine control of macrophage activation is required to prevent inflammatory disease, particularly at barrier sites such as the lung. However, the dominant mechanisms that regulate pulmonary MΦs during inflammation are currently poorly understood. Here we show that airway MΦs are substantially less able to respond to the canonical type-2 cytokine IL-4, which underpins allergic disease and parasite worm infections, than lung tissue or peritoneal cavity MΦs. We reveal that MΦ hypo-responsiveness to IL-4 is dictated by the lung environment, though independent of the host microbiota or the prominent lung extracellular matrix components surfactant protein D and mucin 5b. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
13 Samples
Download data: TXT
Series
Accession:
GSE126309
ID:
200126309
14.

Human resistin alters lung mRNA expression from helminth-infected lungs.

(Submitter supplied) Goal: To examine the effects of human resistin during helminth infection. Methodology: To examine the function of human resistin (hResistin), we utilized transgenic mice expressing the human resistin gene along with its entire regulatory region (hRetnTg+). Following infection with the helminth Nippostrongylus brasiliensis, whole lung RNA was sequenced in hRetnTg+ mice, control hRetnTg- and naïve mice. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
10 Samples
Download data: XLSX
Series
Accession:
GSE60537
ID:
200060537
15.

Characterization of ST2+ and ST2- mTh cells in helminth infection

(Submitter supplied) CD4+T cells are differentiated into Th1, Th2, Th17 and Treg cells after Antigen presentation by other cell types such as dendritic cells, macrophages and B cells in Lymph nodes. Those differentiated CD4+T cells are subdivided into cell subsets by their producing cytokines and surface markers. We recently identified that ST2 expressing Th2 cells highly produced IL-5 comparing to ST2- Th2 cells in helminth infection. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18480
12 Samples
Download data: TXT
Series
Accession:
GSE120173
ID:
200120173
16.

Neuropeptide CGRP limits ILC2 responses and constrains type 2 inflammation

(Submitter supplied) Innate and adaptive lymphocytes work in concert to maintain tissue homeostasis and to mediate host defense at mucosal barriers. Herein, we used single cell analysis to show substantial diversity of gene expression in ILCs and T helper cells during a helminth infection in the lung. Notably, we found that the Calca gene, which is spliced to generate the neuropeptide CGRP, was selectively transcribed in ILC2s and Th2 cells in an activation dependent manner. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21493
54 Samples
Download data: BW, MTX, TSV
Series
Accession:
GSE131996
ID:
200131996
17.

Expression data from mouse Nuocytes

(Submitter supplied) Nuocytes are a recently described cell that responds to both IL-25 and IL-33 and produce high levels of IL-13 and IL-5
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
5 Samples
Download data: CEL, CHP
Series
Accession:
GSE25890
ID:
200025890
18.

The JMJD3-IRF4 axis regulates M2 macrophage polarization and host responses against helminth infection

(Submitter supplied) Polarization of macrophages to M1 or M2 cells is important for mounting responses against bacterial and helminth infection respectively. Jumonji domain containing 3 (JMJD3), a histone 3 K27 demethylase, has been implicated in the activation of macrophages. Here we show that JMJD3 is essential for M2 macrophage polarization to helminth infection and chitin, though JMJD3 is dispensable for M1 responses. more...
Organism:
Mus musculus
Type:
Expression profiling by array; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL1261 GPL10010
6 Samples
Download data: BED, CEL
Series
Accession:
GSE23306
ID:
200023306
19.

Genome wide trimethyl-H3K27 distibution in macrophages from wild-type and Jmjd3-/- macrophages.

(Submitter supplied) Jmjd3 is trimethyl H3K27 specific demethylase required for M2 macrophage polarization. Genomic fragments obtained from wild-type and Jmjd3-/- mouse macrophages were immunoprecipitated with anti H3K27me3 Ab, and deep sequencing was performed.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL10010
2 Samples
Download data: BED
Series
Accession:
GSE23297
ID:
200023297
20.

Expression data of LPS-stimulated bone marrow macrophages induced by M-CSF from wild-type and Jmjd3-/- mice.

(Submitter supplied) Jmjd3 is critical for proper M2 macropahge inducution in response to M-CSF and showed defects in response to LPS. We used microarrays to examine gene expression profiles in wild-type and Jmjd3-/- M-CSF-derived macrophages.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
4 Samples
Download data: CEL
Series
Accession:
GSE23180
ID:
200023180
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