» Articles » PMID: 34220520

The Role and Mechanism of Histone Deacetylases in Acute Kidney Injury

Overview
Journal Front Pharmacol
Date 2021 Jul 5
PMID 34220520
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Acute kidney injury (AKI) is a common clinical complication with an incidence of up to 8-18% in hospitalized patients. AKI is also a complication of COVID-19 patients and is associated with an increased risk of death. In recent years, numerous studies have suggested that epigenetic regulation is critically involved in the pathophysiological process and prognosis of AKI. Histone acetylation, one of the epigenetic regulations, is negatively regulated by histone deacetylases (HDACs). Increasing evidence indicates that HDACs play an important role in the pathophysiological development of AKI by regulation of apoptosis, inflammation, oxidative stress, fibrosis, cell survival, autophagy, ATP production, and mitochondrial biogenesis (MB). In this review, we summarize and discuss the role and mechanism of HDACs in the pathogenesis of AKI.

Citing Articles

Inhibition of HDAC8 mitigates AKI by reducing DNA damage and promoting homologous recombination repair.

Wang Y, Yu C, Yu J, Shen F, Du X, Liu N J Cell Mol Med. 2024; 28(18):e70114.

PMID: 39317961 PMC: 11422176. DOI: 10.1111/jcmm.70114.


Histone deacetylase expression following cisplatin-induced acute kidney injury in male and female mice.

Nguyen H, Gales A, Monteiro-Pai S, Oliver A, Harris N, Montgomery A Am J Physiol Renal Physiol. 2024; 327(4):F623-F636.

PMID: 39116350 PMC: 11483084. DOI: 10.1152/ajprenal.00132.2024.


Sex-specific epigenetic programming in renal fibrosis and inflammation.

Kumar P, Brooks H Am J Physiol Renal Physiol. 2023; 325(5):F578-F594.

PMID: 37560775 PMC: 11550885. DOI: 10.1152/ajprenal.00091.2023.


Histone Deacetylases Cooperate with NF-κB to Support the Immediate Migratory Response after Zebrafish Pronephros Injury.

Zhuang M, Scholz A, Walz G, Yakulov T Int J Mol Sci. 2022; 23(17).

PMID: 36076983 PMC: 9455417. DOI: 10.3390/ijms23179582.


Class IIa histone deacetylase inhibition ameliorates acute kidney injury by suppressing renal tubular cell apoptosis and enhancing autophagy and proliferation.

Li J, Yu C, Shen F, Cui B, Liu N, Zhuang S Front Pharmacol. 2022; 13:946192.

PMID: 35935816 PMC: 9354984. DOI: 10.3389/fphar.2022.946192.


References
1.
Malis C, Bonventre J . Susceptibility of mitochondrial membranes to calcium and reactive oxygen species: implications for ischemic and toxic tissue damage. Prog Clin Biol Res. 1988; 282:235-59. View

2.
Seto E, Yoshida M . Erasers of histone acetylation: the histone deacetylase enzymes. Cold Spring Harb Perspect Biol. 2014; 6(4):a018713. PMC: 3970420. DOI: 10.1101/cshperspect.a018713. View

3.
Choi S, Piao Z, Jin L, Kim J, Kim G, Ryu Y . Piceatannol Attenuates Renal Fibrosis Induced by Unilateral Ureteral Obstruction via Downregulation of Histone Deacetylase 4/5 or p38-MAPK Signaling. PLoS One. 2016; 11(11):e0167340. PMC: 5130266. DOI: 10.1371/journal.pone.0167340. View

4.
Chen S, Bellew C, Yao X, Stefkova J, Dipp S, Saifudeen Z . Histone deacetylase (HDAC) activity is critical for embryonic kidney gene expression, growth, and differentiation. J Biol Chem. 2011; 286(37):32775-89. PMC: 3173185. DOI: 10.1074/jbc.M111.248278. View

5.
Gao R, Chen J, Hu Y, Li Z, Wang S, Shetty S . Sirt1 deletion leads to enhanced inflammation and aggravates endotoxin-induced acute kidney injury. PLoS One. 2014; 9(6):e98909. PMC: 4045768. DOI: 10.1371/journal.pone.0098909. View