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High-throughout sequencing of RAW264.7 cells treated with LPS and Harmine

ABSTRACT: High-throughout sequencing of RAW264.7 cells treated with LPS and Harmine

PROVIDER: PRJNA1111748 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR29029516_1.fastq.gz	Fastqsanger.gz
	SRR29029516_2.fastq.gz	Fastqsanger.gz
	SRR29029517_1.fastq.gz	Fastqsanger.gz
	SRR29029517_2.fastq.gz	Fastqsanger.gz
	SRR29029518_1.fastq.gz	Fastqsanger.gz

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High-throughout sequencing of RAW264.7 cells treated with LPS and Harmine

Project description:After stimulation of RAW264.7 cells with LPS and Harmine, high-throughput sequencing technology was used to explore the changes in the inflammation level of RAW cells and the enrichment of signaling pathways after LPS and Harmine treatment, and to find an interesting target pathway.

2024-05-20 | GSE267507 | GEO

miRNA profiling in RAW264.7 cells treated without or with LPS and IFNγ

Project description:We have identified a number of miRNAs that are differentially expressed in LPS and IFNγ treated RAW264.7 cells, as compared to untreated cells. Microarray and quantitative real-time PCR (qRT-PCR) results showed that miR-103 decreased while the STAT1 expression increased substantially in RAW264.7 derived M1 macrophage, and there was a significant negative correlation between miR-103 and STAT1.Overexpression of miR-103 suppressed M1 polarization by inhibiting STAT1/IRF1 signaling pathway and vice versa in vitro. STAT1 is a direct target of of miR-103.

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RNA-seq in RAW264.7 cells after silence of Synbindin in response to LPS

Project description:RAW264.7 cells were transfected with Synbindin siRNA for 48hours, then 100ng/ml LPS were treated cells for 4 hours. Before and after LPS stimulation, cells were collected and RNA were extracted for RNA-seq.

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miRNA profiling in RAW264.7 cells treated without or with LPS and IFNγ

Project description:miRNA profiling in RAW264.7 cells treated without or with LPS and IFNγ

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Anti-inflammatory role of low intensity pulsed ultrasound in inhibiting LPS-induced M1 polarization of RAW264.7 via Wnt2b/AXIN/β-catenin

Project description:Low-intensity pulsed ultrasound (LIPUS) is a special type of low intensity ultrasound. In periodontal disease, LIPUS was applied as an adjuvant and non-invasive therapeutic treatment. While, the specific mechanism of LIPUS in the treatment of periodontal disease is not quite clear.RAW264.7 cells were induced to M1/M2 macrophage-like polarization by LPS/IL4. LIPUS was performed to stimulate RAW264.7 cells at an intensity of 45 mW/cm2, 25 min, interval 24 h, twice. The polyA mRNA sequencing of LPS induced RAW264.7 cells, LPS induced and LIPUS treated RAW264.7 cells were conducted.Our results suggested that LIPUS played an anti-inflammatory role by inhibiting LPS-induced M1 polarization of RAW264.7 cells in an Wnt2b/AXIN/β-catenin dependent way. LIPUS may inhibit inflammation in periodontal diseases by regulating macrophage differentiation, so as to play a therapeutic role in periodontal diseases.

2024-10-15 | GSE273466 | GEO

AF9/MLLT3 ChIP-Seq in LPS-stimulated RAW264.7 cells

Project description:We sought to characterize the genomic localization of the YEATS domain protein AF9 in the macrophage-like cell line RAW 264.7 +/- LPS stimulation and +/- sodium crotonate pretreatment. We performed chromatin immunoprecipitation followed by massively parallel sequencing (ChIP-seq) for endogenous AF9 or for a FLAG-tagged AF9 transgene in RAW264.7 or a RAW264.7 cell line engineered to express FLAG-AF9, respectively.

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Effect of Drp1 inhibitor on gene expression profiles of RAW264.7 cells at 24 hours or 96 hours after LPS and IFN-γ stimulation

Project description:Effects of Drp1 inhibitor Mdivi-1 on gene expression profiles of LPS and IFN-γ-treated RAW264.7 cells were examined.

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H3K4methylation in Setd1a loss-of-function Raw264.7 cells upon LPS or Dex+LPS stimulation

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2020-12-31 | GSE138017 | GEO

LPS effects on macrophages

Project description:RAW264.7 murine macrophages treated with LPS Keywords: time-course

2004-06-05 | GSE1459 | GEO

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