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Links from GEO DataSets

Items: 20

1.

Gene expression profiling of the duodenum and ileum of mice lacking enteroendocrine cells

(Submitter supplied) Background and aims: Enteroendocrine cells (EECs) and their hormones are essential regulators of whole-body energy homeostasis. EECs sense luminal nutrients and microbial metabolites and subsequently secrete a variety of hormones acting locally or at distance. Impaired development of EECs during embryogenesis is life-threatening in newborn mice and humans due to compromised nutrient absorption. However, the physiological importance of the EEC system in adult mice has not been directedly studied. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
16 Samples
Download data: TSV
Series
Accession:
GSE221473
ID:
200221473
2.

Gene expression profiling of the duodenum and ileum of mice lacking enteroendocrine cells and fed a high fat diet

(Submitter supplied) Background and aims: Enteroendocrine cells (EECs) and their hormones are essential regulators of whole-body energy homeostasis. EECs sense luminal nutrients and microbial metabolites and subsequently secrete a variety of hormones acting locally or at distance. Impaired development of EECs during embryogenesis is life-threatening in newborn mice and humans due to compromised nutrient absorption. However, the physiological importance of the EEC system in adult mice has not been directedly studied. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30172
16 Samples
Download data: TSV
Series
Accession:
GSE224026
ID:
200224026
3.

Effect of a high fat diet on gene expression in enteroendocrine cells of the mouse jejunum

(Submitter supplied) To identify the genes differentially expressed in jejunal enteroendocrine cells (EECs) under a high fat diet we purified EEC (eYFP+) and non-EEC(eYFP-) using FACS from jejunal villi of Neurog3eYFP/+ mice (Mellitzer et al, Mol. Endo 2004) fed with a normal chow or high fat diet (HFD). In Neurog3eYFP/+ mice enteroendocrine progenitors and their descendants are labeled with eYFP. We then purified the RNA and perfomed gene exspression profiling using RNAseq.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
12 Samples
Download data: TSV
Series
Accession:
GSE218600
ID:
200218600
4.

Single-cell sequencing of human intestnal organoids with and without enteroendocrine cells (EECs)

(Submitter supplied) We generated pluripotent stem cell-derived human intestinal organoids with (n=2) and without (n=1) EECs and performed single-cell sequencing after their transplantation under the mouse kidney capsule to evaluate similarities and differences in the absence of enteroendocrine cells.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
3 Samples
Download data: H5AD
Series
Accession:
GSE214852
ID:
200214852
5.

Enteroendocrine cells sense bacterial tryptophan catabolites to activate enteric and vagal neuronal pathways

(Submitter supplied) RNA-seq of isolated zebrafish enteroendocrine cells and other intestinal epithelium cells from germ-free (GF) and conventionalized (CV) zebrafish
Organism:
Danio rerio
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21741
12 Samples
Download data: XLSX
Series
Accession:
GSE151711
ID:
200151711
6.

Neurog3 gene dosage effect on the differentiaiton of intestinal enteroendocrine progenitors

(Submitter supplied) Analysis of FACS-sorted intestinal Neurog3+/+ and Neurog3+/- cells from Neurog3 fluorencent reporter mice carrying two-(+/+) or one- (+/-) Neurog3 alleles. In the intestine, Neurog3 is an enteroendocrine (EE) lineage determinating transcription factor that transiently expressed in early EEC progenitors. By comparison the molecular profiles of Neurog3+/+ and Neurog3+/- cells, we hypothesized that Neurog3 gene dosage regulates the allocation of EE progenitor fates towards EEC vs. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
6 Samples
Download data: TSV
Series
Accession:
GSE149203
ID:
200149203
7.

Transcriptional response of NGN3 J2 enteroids

(Submitter supplied) Enteroendocrine cells are hormonal secreting cells in the gut. However, as they comprise <1% of the total epithelial cell population, studies on their response to stimuli have been limited. Chang-Graham, Danhof, Engevik, and Tomaro-Duchesneau et al (PMID 31029854) developed a model enteroid system to overcome this limitation. By driving expression of NGN3 in human jejunal enteroids, their system allows for analysis of hormonal secretion and transcriptional analysis in response to a stimulus. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
12 Samples
Download data: TXT
Series
Accession:
GSE138350
ID:
200138350
8.

Single cell and bulk RNA sequencing of Enteroendocrine cells from human hormone reporter organoids

(Submitter supplied) Enteroendocrine cell subpopulations were sorted by positivity for endogenous knock-in reporters in different hormones. Unbiased and biased FAC sorting was performed and coupled to single cell sorting by the SortSeq protocol (Muraro et al., 2016) and bulk sequencing.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
28 Samples
Download data: CSV
Series
Accession:
GSE146799
ID:
200146799
9.

Pancreatic and intestinal endocrine cells share common transcriptomic signatures and gene regulatory networks

(Submitter supplied) Background: Endocrine cells of the digestive system, including the pancreatic endocrine cells (PECs) clustered in the islets of Langerhans and the enteroendocrine cells (EECs) scattered in the intestinal epithelium, play an important role in metabolism. Although EECs and PECs are located in distinct organs, they share many features and several common genes control their differentiation. In this study, we investigated comprehensively the similarity of EECs and PECs by defining their transcriptomic landscape and comparing the regulatory networks controlled by pax6b, a key player in both EECs and PECs. more...
Organism:
Danio rerio
Type:
Expression profiling by high throughput sequencing
Platform:
GPL14875
13 Samples
Download data: TXT
Series
Accession:
GSE149081
ID:
200149081
10.

Mapping prohormone processing by proteases in human enteroendocrine cells using genetically engineered organoid models

(Submitter supplied) Bulk RNA sequencing was performed on organoids differentiated towards enteroendocrine cells in the presence and absence of BMP
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
4 Samples
Download data: CSV
Series
Accession:
GSE212636
ID:
200212636
11.

ISX-9 manipulates endocrine progenitor fate revealing conserved intestinal lineages in mouse and human

(Submitter supplied) Objective: Enteroendocrine cells (EECs) survey the gut luminal environment and co-ordinate hormonal, immune and neuronal responses to it. They exhibit well characterized physiological roles ranging from the control of local gut function to whole body metabolism, but little is known regarding the regulatory networks controlling their differentiation, especially in human gut. The small molecule Isoxazole-9 (ISX-9) has been shown to stimulate neuronal and pancreatic beta-cell differentiation, both closely related to EEC differentiation. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
2 Samples
Download data: PDF, TSV
Series
Accession:
GSE143221
ID:
200143221
12.

An approach to intersectionally target mature enteroendocrine cells in the small intestine of mice

(Submitter supplied) Enteroendocrine cells (EECs) constitute only a small proportion of Villin-1 (Vil1)-expressing intestinal epithelial cells (IECs) of the gastrointestinal tract; yet, in sum, they build the largest endocrine organ of the body, with each of them storing and releasing a distinct set of peptides for the control of feeding behavior, glucose metabolism, and gastrointestinal motility. Like all IEC types, EECs are continuously renewed from intestinal stem cells in the crypt base and terminally differentiate into mature subtypes while moving up the crypt-villus axis. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
3 Samples
Download data: MTX, TSV
Series
Accession:
GSE250433
ID:
200250433
13.

Mouse duodenal enteroendocrine transcriptome

(Submitter supplied) Using genetically modifed mice to express fluorescent reporter in proglucagon expressing cells (GluVenus) or in all enteroendocrine cells (NeuroD1), we purifed positive and negative cells by FACS from duodenal epithelial cells and identified transcripts enriched in positive populations
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
11 Samples
Download data: TXT
Series
Accession:
GSE114913
ID:
200114913
14.

Human enteroendocrine cell transcriptomic profiling

(Submitter supplied) We purified two populations of human jejunal enteroendocrine cells (GLP1+ and GLP1-) by FACS and identified transcripts enriched in endocrine cell lineages.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
39 Samples
Download data: TXT
Series
Accession:
GSE114853
ID:
200114853
15.

Osteopontin Exacerbates High-Fat Diet-induced Metabolic Disorders in a microbiome-dependent Manner

(Submitter supplied) Gut microbiota is involved in metabolic disorders. However, microbiome-based therapeutic interventions are not always effective, which might be due to interference of the host factors. Here, we first identified a strong positive correlation between OPN levels and BMI in humans. Next, we confirmed that OPN could aggravate high-fat diet induced metabolic disorders in mice. Importantly, we found that fecal microbiota transplantation from OPN-deficient mice significantly alleviated metabolic disorders in WT mice. more...
Organism:
Bacteria; feces metagenome; Mus musculus
Type:
Other; Expression profiling by high throughput sequencing
4 related Platforms
126 Samples
Download data: TXT, XLS, XLSX
Series
Accession:
GSE216386
ID:
200216386
16.

Comparison of enteroendocrine cells and pancreatic β-cells using gene expression profiling and insulin gene methylation

(Submitter supplied) In this study, similarities between EECs and β-cells were evaluated in detail. To obtain specific subtypes of EECs, cell sorting by flow cytometry was conducted from STC-1 cells (a heterogenous EEC line), and each single cell was cultured and passaged. Five EEC subtypes were established according to hormone expression, measured by quantitative RT-PCR and immunostaining: L, K, I, G and S cells expressing glucagon-like peptide-1, glucose-dependent insulinotropic polypeptide, cholecystokinin, gastrin and secretin, respectively. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL16570
39 Samples
Download data: CEL, CHP
Series
Accession:
GSE119747
ID:
200119747
17.

Transcription factor dynamics, oscillation, and functions in human enteroendocrine cell differentiation

(Submitter supplied) Enteroendocrine cells (EECs) secrete serotonin (enterochromaffin [EC] cells) or specific peptide hormones (non-EC cells) that serve vital metabolic functions. The basis for terminal EEC diversity remains obscure. By forcing activity of the transcription factor (TF) NEUROG3 in 2D cultures of human intestinal stem cells, we replicated physiologic EEC differentiation and examined transcriptional and cis-regulatory dynamics that culminate in discrete cell types. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing; Other
Platforms:
GPL20795 GPL24676
101 Samples
Download data: BED, BW, MTX, TBI, TSV
Series
Accession:
GSE238276
ID:
200238276
18.

Transcription factor dynamics, oscillation, and functions in human enteroendocrine cell differentiation [Multiome-seq]

(Submitter supplied) To investigate the regulation of human enteroendocrine cell differentiation, we established Neurog3ER inducible cell lines. We then performed simultaneous gene expression profiling and chromatin analysis at single cell level using data obtained from Multiome-seq at various time points.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24676
28 Samples
Download data: BED, MTX, TBI, TSV, TXT
Series
Accession:
GSE238275
ID:
200238275
19.

Transcription factor dynamics, oscillation, and functions in human enteroendocrine cell differentiation [scRNA-seq]

(Submitter supplied) To investigate the regulation of human enteroendocrine cell differentiation, we established Neurog3ER inducible cell lines. We then performed gene expression profiling analysis at single cell level using data obtained from single cell RNA-seq of at various time points.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
6 Samples
Download data: MTX, TSV, TXT
Series
Accession:
GSE238274
ID:
200238274
20.

Transcription factor dynamics, oscillation, and functions in human enteroendocrine cell differentiation [Cut&Run]

(Submitter supplied) To investigate the regulation of human enteroendocrine cell differentiation, we established Neurog3ER inducible cell lines. We then analyzed ASCL1 and NEUROD1 binding using data obtained from CUT&RUN of at 96h.
Organism:
Homo sapiens
Type:
Other
Platform:
GPL20795
12 Samples
Download data: BW, TXT
Series
Accession:
GSE238272
ID:
200238272
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