Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Oxygen-dependent changes and lysosome activity-dependent changes of gene expression in BMDM after LPS treatment

ABSTRACT: This SuperSeries is composed of the SubSeries listed below.

ORGANISM(S): Mus musculus

PROVIDER: GSE181643 | GEO | 2024/04/06

REPOSITORIES: GEO

ACCESS DATA

Json Xml

Dataset's files

Source:

			Action	DRS
		Other

Items per page:

1 - 1 of 1

Similar Datasets

Lysosome activity-dependent changes of gene expression in BMDM after LPS treatment

Project description:We report changes of gene expression in lysosome-inhibited BMDM after LPS treatment.

2024-04-06 | GSE181642 | GEO

Oxygen-dependent changes and lysosome activity-dependent changes of gene expression in BMDM after LPS treatment

Project description:Oxygen-dependent changes and lysosome activity-dependent changes of gene expression in BMDM after LPS treatment

| PRJNA752788 | ENA

Oxygen-dependent changes of gene expression in BMDM after LPS treatment

Project description:We report oxygen-dependent changes of gene expression in BMDM after LPS treatment.

2024-04-06 | GSE181641 | GEO

Lysosome activity-dependent changes of gene expression in BMDM after LPS treatment

Project description:Lysosome activity-dependent changes of gene expression in BMDM after LPS treatment

| PRJNA752789 | ENA

Oxygen-dependent changes of gene expression in BMDM after LPS treatment

Project description:Oxygen-dependent changes of gene expression in BMDM after LPS treatment

| PRJNA752790 | ENA

Age-dependent changes in the LPS-induced transcriptome of bovine dermal fibroblasts occurs without major changes in the methylome

Project description:This SuperSeries is composed of the SubSeries listed below. Refer to individual Series

2014-12-23 | E-GEOD-61168 | biostudies-arrayexpress

Glutamine-dependent lysosome homeostatic changes induced by starvation and lysosome inhibition.

Project description:Lysosomes are a major organelle for degrading macromolecules. When deprived of nutrients, cells activate the autophagy and lysosome biogenesis pathways to recycle cytoplasmic materials and to increase lysosomal degradation capacity for survival, respectively. We have identified a condition in which cells accumulated enlarged lysosomes upon starvation and lysosome inhibition. Selective autophagy and inhibition of the mechanistic target of rapamycin (mTOR) in combination with lysosome inhibition were not able to induce this phenomenon. Conversely, knocking out autophagy genes, ATG5 or ATG7, had no effects on the enlarged lysosome formation. This suggests that the enlarged lysosome formation is an autophagy independent process. Remarkably, adding glutamine to the treatment can prevent formation of the enlarged lysosomes and dissipate the pre-existing ones. Furthermore, the nucleus/cytoplasm translocation of the transcription factor EB (TFEB), but not mTOR activity, correlates with the formation/dissipation of enlarged lysosomes. Knockdown of TFEB, however, suggests that TFEB-mediated lysosome biogenesis is not directly involved in the process. These results indicate that there is a novel mechanism by which lysosome homeostasis can be regulated under certain stress conditions.

| S-EPMC6392085 | biostudies-literature

The miRNA pathway controls rapid changes in activity-dependent synaptic structure at the Drosophila melanogaster neuromuscular junction

Project description:This SuperSeries is composed of the SubSeries listed below. Refer to individual Series

2013-02-01 | E-GEOD-43945 | biostudies-arrayexpress

Age-dependent changes in the LPS-induced transcriptome of bovine dermal fibroblasts occurs without major changes in the methylome

Project description:This SuperSeries is composed of the SubSeries listed below.

2014-12-23 | GSE61168 | GEO

Pig BMDM +/- LPS

Project description:RNA sequencing of pig (Sus scrofa) bone marrow derived macrophages (BMDMs), both unstimulated and 7 hours after stimulation with lipopolysaccharide (LPS).

| PRJEB22536 | ENA

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data