Acetyl-CoA synthetase 2 induces pyroptosis and inflammation of renal epithelial tubular cells in sepsis-induced acute kidney injury by upregulating the KLF5/NF-κB pathway
- Cell Commun Signal. 2024 Mar 21;22(1):187. doi: 10.1186/s12964-024-01556-3.
- 1. Department of Nephrology, the Affiliated Hospital of Medical School, Nanjing Drum Tower Hospital, Nanjing University, Jiangsu Province, Nanjing, 210008, China.
- 2. Department of Cardiology, the Affiliated Hospital of Medical School, Nanjing Drum Tower Hospital, Nanjing University, Jiangsu Province, Nanjing, 210008, China.
- 3. Medical School, Nanjing University, Jiangsu Province, Nanjing, 210093, China. [email protected].
- 4. Department of Nephrology, the Affiliated Hospital of Medical School, Nanjing Drum Tower Hospital, Nanjing University, Jiangsu Province, Nanjing, 210008, China. [email protected].
- # Contributed equally.
Background: Pyroptosis of the renal tubular epithelial cells (RTECs) and interstitial inflammation are central pathological characteristics of acute kidney injury (AKI). Pyroptosis acts as a pro-inflammatory form of programmed cell death and is mainly dependent on activation of the NLRP3 inflammasome. Previous studies revealed that Acetyl-CoA synthetase 2 (ACSS2) promotes inflammation during metabolic stress suggesting that ACSS2 might regulate Pyroptosis and inflammatory responses of RTECs in AKI.
Methods and results: The expression of ACSS2 was found to be significantly increased in the renal epithelial cells of mice with lipopolysaccharide (LPS)-induced AKI. Pharmacological and genetic strategies demonstrated that ACSS2 regulated NLRP3-mediated Caspase-1 activation and Pyroptosis through the stimulation of the KLF5/NF-κB pathway in RTECs. The deletion of ACSS2 attenuated renal tubular pathological injury and inflammatory cell infiltration in an LPS-induced mouse model, and ACSS2-deficient mice displayed impaired NLRP3 activation-mediated Pyroptosis and decreased IL-1β production in response to the LPS challenge. In HK-2 cells, ACSS2 deficiency suppressed NLRP3-mediated Caspase-1 activation and Pyroptosis through the downregulation of the KLF5/NF-κB pathway. The KLF5 inhibitor ML264 suppressed NF-κB activity and NLRP3-mediated Caspase-1 activation, thus protecting HK-2 cells from LPS-induced Pyroptosis.
Conclusion: Our results suggested that ACSS2 regulates activation of the NLRP3 inflammasome and Pyroptosis by inducing the KLF5/NF-κB pathway in RTECs. These results identified ACSS2 as a potential therapeutic target in AKI.