Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0243026 (
sepsis
)
52,417
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Background:
Acute kidney injury (AKI) refers to a sudden loss of renal function. This study was performed to identify the key RNAs acting in the mechanism of
sepsis
-induced AKI.
Methods:
Microarray dataset GSE94717 (including six
sepsis
-induced AKI samples and three control samples) was downloaded from Gene Expression Omnibus database. Differentially expressed miRNAs (DE-miRNAs) were identified. The miRNA targets were predicted and enrichment analysis was performed. Protein-protein interaction (PPI) and competing endogenous RNA (ceRNA) regulatory networks were constructed. Mouse podocytes were treated with lipopolysaccharide (LPS), following by cell viability and PCR analysis. Cellular apoptosis and the ceRNA network were validated.
Results:
Thirty-one common DE-miRNAs (two up-regulated and 29 down-regulated) by AKI versus control and male AKI versus control were identified. We found the targets of
miR-15a-5p
,
miR-15b-5p
, and
miR-16-5p
were involved in mTOR signaling pathway, and those of
miR-29b-3p and miR-16-5p
were enriched in PI3K-Akt signaling pathway. RNAs including
miR-15b-5p
,
miR-15a-5p
,
miR-107
,
XIST
,
miR-16-5p
, and
cullin 3
gene (
CUL3
) were included in the ceRNA regulatory network. The downregulation of
miR-15a-5p
and
miR-15b-5p
and the upregulation of lncRNA
XIST
and
CUL3
gene were validated using qPCR. The
miR-15a-5p-XIST-CUL3
regulatory axis was identified and was validated. We confirmed that LPS inhibited the growth of mouse podocytes and seven of the ten miRNAs, but upregulated
XIST
and
CUL3
. Transfection analysis showed XIST siRNA enhanced LPS-induced MPC5 cell apoptosis and
miR-15a-5p
inhibitor reserved it, so did as
CUL3
overexpression for
miR-15a-5p
mimics.
Conclusion:
The
miR-15a-5p-XIST-CUL3
regulatory axis was related to the pathogenesis of
sepsis
-induced AKI. Highlights Totally, 31 miRNAs were dysregulated between disease and control groups.
MiR-15a-5p
,
miR-15b-5p
, and
miR-16-5p
were involved in mTOR signaling pathway.
MiR-16-5p
and
miR-29b-3p
were implicated in PI3K-Akt signaling pathway. The miR-15a-5p-XIST-CUL3 axis was critical for
sepsis
-induced AKI.
...
PMID:The
miR-15a-5p-XIST-CUL3
regulatory axis is important for sepsis-induced acute kidney injury. 3165 56