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Transcriptome of human LX-2 hepatic stellate cells treated with the OGT inhibitor OSMI-1

ABSTRACT: Transcriptome of human LX-2 hepatic stellate cells treated with the OGT inhibitor OSMI-1

PROVIDER: PRJNA1016368 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR26057224_1.fastq.gz	Fastqsanger.gz
	SRR26057224_2.fastq.gz	Fastqsanger.gz
	SRR26057225_1.fastq.gz	Fastqsanger.gz
	SRR26057225_2.fastq.gz	Fastqsanger.gz
	SRR26057226_1.fastq.gz	Fastqsanger.gz

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Transcriptome of human LX-2 hepatic stellate cells treated with the OGT inhibitor OSMI-1

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Human hepatic stellate cell line LX-2 activated under acidic culture condition

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Expression data from the hepatic stellate cell line LX-2 after treatment with DMOG and from the liver sinusoidal endothelial cell line TRP3 after incubation with conditioned medium of DMOG-treated LX-2

Project description:Expression data from the hepatic stellate cell line LX-2 after treatment with the prolylhydroxylase inhibitor dimethyloxalylglycine (DMOG) and from the liver sinusoidal endothelial cell line TRP3 after incubation with conditioned medium of DMOG-treated LX-2 Prolyl-hydroxylase inhibitors such as dimethyloxalylglycine (DMOG) stabilize HIF-1α, thereby chemically inducing hypoxia, which also accelerates liver volume increase when given with portal rerouting. We used microarrays to clarify the cellular crosstalk of the different cell types in accelerated liver regeneration by examining the role of hepatic stellate cells (HSC) and liver sinusoidal endothelial cells (LSEC).

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Transcriptome of activated mouse primary hepatic stellate cells treated with the OGT inhibitor OSMI-1

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MicroRNA expression profile of human hepatic stellate cells LX-2 co-cultured with human umbilical cord mesenchymal stem cells and control group

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