BACH1 encourages ferroptosis by activating KDM4C‐mediated COX2 demethylation after cerebral ischemia–reperfusion injury DOI
Tianqi Zhang, Meimei Yang, Chi Ma

et al.

European Journal of Neuroscience, Journal Year: 2023, Volume and Issue: 58(1), P. 2194 - 2214

Published: May 11, 2023

Abstract It has been confirmed that BTB domain and CNC homologue 1 (BACH1) are involved in ferroptosis‐related diseases. However, the function of BACH1 cerebral ischemia–reperfusion injury (CIRI)‐induced ferroptosis remains to be largely unrevealed. First, analysis differentially expressed genes CIRI based on GEO dataset GSE119121 revealed was upregulated CIRI. level prominently increased middle artery occlusion (MCAO)/reperfusion model oxygen–glucose deprivation/reoxygenation cell model. Further, knock‐down markedly reduced iron ion concentration, ROS production, 4‐HNE lipid peroxidation levels facilitated GSH content, viability protein GPX4 SLC7A11, while an pcDNA‐KDM4C or pcDNA‐COX2 combined with siRNA could not enhance this effect. Mechanistically, bound KDM4C promoter transcriptionally activate its expression. Besides, occupy locus COX2 gene, promoting expression by eliminating H3K9me3. Overexpression overturned effects inhibition. In vivo findings displayed brain infraction, pathological damage neuronal loss rate MCAO mice were conspicuously decreased after knock‐down. This study reveals encourages neuroblastoma cells mouse tissues activating KDM4C‐mediated demethylation.

Language: Английский

Regulation of the Nrf2/HO-1 axis by mesenchymal stem cells-derived extracellular vesicles: implications for disease treatment DOI Creative Commons

Hua Su,

Zhongan Wang,

Lidan Zhou

et al.

Frontiers in Cell and Developmental Biology, Journal Year: 2024, Volume and Issue: 12

Published: June 10, 2024

This comprehensive review inspects the therapeutic potential of mesenchymal stem cell-derived extracellular vesicles (MSC-EVs) across multiple organ systems. Examining their impact on integumentary, respiratory, cardiovascular, urinary, and skeletal systems, study highlights versatility MSC-EVs in addressing diverse medical conditions. Key pathways, such as Nrf2/HO-1, consistently emerge central mediators antioxidative anti-inflammatory effects. From expediting diabetic wound healing to mitigating oxidative stress-induced skin injuries, alleviating acute lung even offering solutions for conditions like myocardial infarction renal ischemia-reperfusion injury, demonstrate promising efficacy. Their adaptability different administration routes identifying specific factors opens avenues innovative regenerative strategies. positions candidates future clinical applications, providing a overview medicine.

Language: Английский

Citations

8

Potential effects of different cell death inhibitors in protecting against ischemia-reperfusion injury in steatotic liver DOI Creative Commons

Jiao Junzhe,

Li Meng,

Huang Weifan

et al.

International Immunopharmacology, Journal Year: 2024, Volume and Issue: 128, P. 111545 - 111545

Published: Jan. 19, 2024

Liver ischemia–reperfusion injury (IRI) remains a common issue and with the increasing incidence of Nonalcoholic fatty liver disease (NAFLD), which are more sensitive to IRI, it is crucial explore possible strategy alleviate steatotic IRI. Several modes cell death involved in hepatocytes immune cells during hepatic effects different inhibitors including apoptosis, necroptosis, pyroptosis, ferroptosis IRI have not been investigated. We established 70% model on mice. Apoptosis, pyroptosis were used evaluate their injury, inflammatory response, infiltration. Immunofluorescence immunohistochemical results demonstrated that there progression liver. All four types showed protective effects, but inhibitor Fer-1 VX765 exerted better compared apoptosis Z-VAD necroptosis Nec-1. Further, we found occurred mainly macrophages occured primarily Ferroptosis heaptocytes two major inhibiting these good effects.

Language: Английский

Citations

6

The Regulation of Ferroptosis by Noncoding RNAs DOI Open Access
Xiangnan Zheng, Cen Zhang

International Journal of Molecular Sciences, Journal Year: 2023, Volume and Issue: 24(17), P. 13336 - 13336

Published: Aug. 28, 2023

As a novel form of regulated cell death, ferroptosis is characterized by intracellular iron and lipid peroxide accumulation, which different from other death forms morphologically, biochemically, immunologically. Ferroptosis metabolism, antioxidant defense systems as well various transcription factors related signal pathways. Emerging evidence has highlighted that associated with many physiological pathological processes, including cancer, neurodegeneration diseases, cardiovascular ischemia/reperfusion injury. Noncoding RNAs are group functional RNA molecules not translated into proteins, can regulate gene expression in manners. An increasing number studies have shown noncoding RNAs, especially miRNAs, lncRNAs, circRNAs, interfere the progression modulating ferroptosis-related genes or proteins directly indirectly. In this review, we summarize basic mechanisms regulations focus on recent mechanism for types ncRNAs to conditions, will deepen our understanding regulation provide new insights employing ferroptosis-associated therapeutic strategies.

Language: Английский

Citations

16

Intermittent fasting ameliorates neuronal ferroptosis and cognitive impairment in mice after traumatic brain injury DOI

Qiuyun Yang,

Manrui Li,

Jinyuan Liu

et al.

Nutrition, Journal Year: 2023, Volume and Issue: 109, P. 111992 - 111992

Published: Feb. 4, 2023

Language: Английский

Citations

15

BACH1 encourages ferroptosis by activating KDM4C‐mediated COX2 demethylation after cerebral ischemia–reperfusion injury DOI
Tianqi Zhang, Meimei Yang, Chi Ma

et al.

European Journal of Neuroscience, Journal Year: 2023, Volume and Issue: 58(1), P. 2194 - 2214

Published: May 11, 2023

Abstract It has been confirmed that BTB domain and CNC homologue 1 (BACH1) are involved in ferroptosis‐related diseases. However, the function of BACH1 cerebral ischemia–reperfusion injury (CIRI)‐induced ferroptosis remains to be largely unrevealed. First, analysis differentially expressed genes CIRI based on GEO dataset GSE119121 revealed was upregulated CIRI. level prominently increased middle artery occlusion (MCAO)/reperfusion model oxygen–glucose deprivation/reoxygenation cell model. Further, knock‐down markedly reduced iron ion concentration, ROS production, 4‐HNE lipid peroxidation levels facilitated GSH content, viability protein GPX4 SLC7A11, while an pcDNA‐KDM4C or pcDNA‐COX2 combined with siRNA could not enhance this effect. Mechanistically, bound KDM4C promoter transcriptionally activate its expression. Besides, occupy locus COX2 gene, promoting expression by eliminating H3K9me3. Overexpression overturned effects inhibition. In vivo findings displayed brain infraction, pathological damage neuronal loss rate MCAO mice were conspicuously decreased after knock‐down. This study reveals encourages neuroblastoma cells mouse tissues activating KDM4C‐mediated demethylation.

Language: Английский

Citations

15