Downregulation of circ‐ZNF644 alleviates LPS‐induced HK2 cell injury via miR‐335‐5p/HIPK1 axis

Abstract

Abstract Circular RNA (circRNA) has been confirmed to be involved in regulating sepsis‐induced acute kidney injury (AKI). Our research aims to explore circ‐ZNF644 role in the development of sepsis‐induced AKI. Lipopolysaccharide (LPS) was used to induce kidney tubular epithelial cell (HK2) injury. ELISA assay was performed to measure the concentrations of inflammation factors. Cell functions were determined by cell counting kit 8 assay, EdU assay and flow cytometry. Protein expression was evaluated by Western blot analysis. Quantitative real‐time PCR was used to detect relative expression of circ‐ZNF644, miR‐335‐5p and homeodomain‐interacting protein kinase 1 (HIPK1). RNA interaction was confirmed by dual‐luciferase reporter assay and RIP assay. LPS enhanced HK2 cell inflammation, oxidative stress, apoptosis, and reduced proliferation. Circ‐ZNF644 was overexpressed in sepsis‐induced AKI patients. Circ‐ZNF644 knockdown suppressed LPS‐induced HK2 cell injury, and this effect could be revoked by miR‐335‐5p inhibitor. MiR‐335‐5p was sponged by circ‐ZNF644, and its expression was downregulated in sepsis‐induced AKI patients. HIPK1 was targeted by miR‐335‐5p, and its expression could be suppressed by circ‐ZNF644 knockdown. MiR‐335‐5p had an inhibition effect on HK2 cell injury induced by LPS, and HIPK1 overexpression could reverse this effect. Circ‐ZNF644 knockdown relieved LPS‐induced HK2 cell injury through the miR‐335‐5p/HIPK1 axis, confirming that circ‐ZNF644 contributed to sepsis‐induced AKI.