Published in:
Open Access 01-12-2024 | Acute Kidney Injury | Research
Circular RNA hsa_circ_0005519 contributes to acute kidney injury via sponging microRNA-98-5p
Published in: BMC Nephrology | Issue 1/2024
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Background
This study intends to explore the role and molecular mechanism of hsa_circ_0005519 in acute kidney injury (AKI).
Methods
We conducted reverse transcription-qPCR for human serum to determine levels of hsa_circ_0005519 in AKI patients and healthy controls. Hsa_circ_0005519 was inhibited for expression in HK-2 cells using specific siRNAs. A number of techniques, MTT and ELISA assays, were used to analyze the potential role of hsa_circ_0005519 in cell viability, oxidative stress, and inflammation of LPS-induced HK-2 cells.
results
The serum of patients with AKI exhibited a significant increase in hsa_circ_0005519 expression, compared with healthy controls. Hsa_circ_0005519 was knockdown by siRNA, and its knockdown led to cell viability increase in LPS-induced HK-2 cells. Inhibition of hsa_circ_0005519 can reverse the TNF-α, IL-6 and IL-1β increase in LPS-induced HK-2 cells. Inhibiting hsa_circ_0005519 led to downregulation of MPO and MDA levels. MiR-98-5p was a downstream miRNA for hsa_circ_0005519. MiR-98-5p can offset the effects of hsa_circ_0005519 on LPS-induced HK-2 cells. IFG1R was a target gene for miR-98-5p.
Conclusions
These findings indicate that the highly expressed hsa_circ_0005519 plays a promoting role in AKI.