NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE189412 Query DataSets for GSE189412
Status Public on Jun 01, 2022
Title METTL3 Regulates LPS-Induced Inflammatory Response via the NOD1 Signaling Pathway
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary Inflammation is normally a protective response to defend and restore homeostasis; nonresolving inflammation is a major driver of immune disorders. N6-methyladenosine (m6A) is a prevalent mRNA modification that plays a crucial function in multiple biological processes. The effect of m6A on the immune response has recently been reported. However, the effect is unclear, and the results are contradictory. In this study, the expression of total m6A and the methyltransferase METTL3 decreased in LPS-stimulated macrophages. METTL3 knockdown significantly upregulated expression of proinflammatory cytokines, including TNF-α, IL-6 and NO. RNA sequencing analysis showed that the upregulated genes were enriched in inflammation-related signaling pathways and that the NOD-like receptor signaling pathway might be the target molecules of METTL3. METTL3 depletion resulted in upregulation of the NOD1 pathway without impacting NOD2. Moreover, the increase in proinflammatory cytokines induced by METTL3 knockdown was reversed by blocking the NOD1 pathway using the NOD-IN-1 and ML130 specific inhibitors. Mechanistically, METTL3 knockdown promoted the mRNA expression and stability of NOD1 and RIPK2, and the same results were detected in m6A-binding protein YTHDF1- or YTHDF2-silenced cells. All findings suggested that METTL3 depletion inhibits the degradation of NOD1 and RIPK2 mRNA mediated by YTHDF1 and YTHDF2, which upregulate the NOD1 pathway and subsequently promote the LPS-induced inflammatory response in macrophages.
 
Overall design two repeates of mRNA from shControl RAW264.7 cells and two repeates of mRNA from shMETTL3 RAW264.7 cells
 
Contributor(s) Cai Y
Citation missing Has this study been published? Please login to update or notify GEO.
Submission date Nov 23, 2021
Last update date Jun 01, 2022
Contact name Yongjie Cai
E-mail(s) [email protected]
Phone 18826073519
Organization name SUN YAT-SEN UNIVERSITY
Lab Guangdong Provincial Key Laboratory of Stomatology
Street address 56 Ling Yuan Xi Road
City Guangzhou
State/province Guangdong
ZIP/Postal code 510055
Country China
 
Platforms (1)
GPL23479 BGISEQ-500 (Mus musculus)
Samples (4)
GSM5701168 Control_1
GSM5701169 Control_2
GSM5701170 shMettl3_1
Relations
BioProject PRJNA782970

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE189412_gene_expression.txt.gz 706.5 Kb (ftp)(http) TXT
GSE189412_gene_expression.xlsx 2.0 Mb (ftp)(http) XLSX
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap