ADSCs-derived exosomes suppress macrophage ferroptosis via the SIRT1/NRF2 signaling axis to alleviate acute lung injury in sepsis DOI

Xiaozhi Bai,

Yang Liu, Jiaqi Liu

et al.

International Immunopharmacology, Journal Year: 2024, Volume and Issue: 146, P. 113914 - 113914

Published: Dec. 27, 2024

Language: Английский

Iron homeostasis and ferroptosis in human diseases: mechanisms and therapeutic prospects DOI Creative Commons

Qin Ru,

Yusheng Li,

Lin Chen

et al.

Signal Transduction and Targeted Therapy, Journal Year: 2024, Volume and Issue: 9(1)

Published: Oct. 14, 2024

Iron, an essential mineral in the body, is involved numerous physiological processes, making maintenance of iron homeostasis crucial for overall health. Both overload and deficiency can cause various disorders human diseases. Ferroptosis, a form cell death dependent on iron, characterized by extensive peroxidation lipids. Unlike other kinds classical unprogrammed death, ferroptosis primarily linked to disruptions metabolism, lipid peroxidation, antioxidant system imbalance. Ferroptosis regulated through transcription, translation, post-translational modifications, which affect cellular sensitivity ferroptosis. Over past decade or so, diseases have been as part their etiology, including cancers, metabolic disorders, autoimmune diseases, central nervous cardiovascular musculoskeletal Ferroptosis-related proteins become attractive targets many major that are currently incurable, some regulators shown therapeutic effects clinical trials although further validation potential needed. Therefore, in-depth analysis its molecular mechanisms may offer additional strategies prevention treatment. In this review, we discuss significance contribution etiology development along with evidence supporting targeting approach. Importantly, evaluate recent promising interventions, providing guidance future targeted treatment therapies against

Language: Английский

Citations

60

The Interplay between Ferroptosis and Neuroinflammation in Central Neurological Disorders DOI Creative Commons

Yejia Xu,

Bowen Jia,

Jing Li

et al.

Antioxidants, Journal Year: 2024, Volume and Issue: 13(4), P. 395 - 395

Published: March 26, 2024

Central neurological disorders are significant contributors to morbidity, mortality, and long-term disability globally in modern society. These encompass neurodegenerative diseases, ischemic brain traumatic injury, epilepsy, depression, more. The involved pathogenesis is notably intricate diverse. Ferroptosis neuroinflammation play pivotal roles elucidating the causes of cognitive impairment stemming from these diseases. Given concurrent occurrence ferroptosis due metabolic shifts such as iron ROS, well their critical central nervous disorders, investigation into co-regulatory mechanism has emerged a prominent area research. This paper delves mechanisms along with interrelationship. It specifically emphasizes core molecules within shared pathways governing neuroinflammation, including SIRT1, Nrf2, NF-κB, Cox-2, iNOS/NO·, how different immune cells structures contribute dysfunction through mechanisms. Researchers’ findings suggest that mutually promote each other may represent key factors progression disorders. A deeper comprehension common pathway between cellular holds promise for improving symptoms prognosis related

Language: Английский

Citations

18

Quercetin Modulates Ferroptosis via the SIRT1/Nrf−2/HO−1 Pathway and Attenuates Cartilage Destruction in an Osteoarthritis Rat Model DOI Open Access

Hongri Ruan,

Tingting Zhu, Tiantian Wang

et al.

International Journal of Molecular Sciences, Journal Year: 2024, Volume and Issue: 25(13), P. 7461 - 7461

Published: July 7, 2024

Osteoarthritis (OA) is the most common joint disease, causing symptoms such as pain, swelling, and deformity, which severely affect patients' quality of life. Despite advances in medical treatment, OA management remains challenging, necessitating development safe effective drugs. Quercetin (QUE), a natural flavonoid widely found fruits vegetables, shows promise due to its broad range pharmacological effects, particularly various degenerative diseases. However, role preventing progression underlying mechanisms remain unclear. In this study, we demonstrated that QUE has protective effect against both vivo vitro, elucidated molecular mechanisms. inhibited expression IL-1β-induced chondrocyte matrix metalloproteinases (MMP3 MMP13) inflammatory mediators INOS COX-2. It also promoted collagen II, thereby extracellular (ECM). Mechanistically, exerts on chondrocytes by activating SIRT1/Nrf-2/HO-1 inhibiting ferroptosis. Similarly, an rat model induced anterior cruciate ligament transection (ACLT), treatment improved articular cartilage damage, reduced normalized abnormal subchondral bone remodeling. serum IL-1β, TNF-α, MMP3, CTX-II, COMP, slowing OA. chondroprotective effects oxidative damage ferroptosis through pathway, effectively alleviating rats.

Language: Английский

Citations

11

Sappanone a alleviates osteoarthritis progression by inhibiting chondrocyte ferroptosis via activating the SIRT1/Nrf2 signaling pathway DOI
Zhi Zhang,

Nan-Zhi Zhang,

Meng Li

et al.

Naunyn-Schmiedeberg s Archives of Pharmacology, Journal Year: 2024, Volume and Issue: unknown

Published: June 4, 2024

Language: Английский

Citations

6

The Role of Ferroptosis in Osteoarthritis: Progress and Prospects DOI
Weibei Sheng,

Shuai Liao,

Deli Wang

et al.

Biochemical and Biophysical Research Communications, Journal Year: 2024, Volume and Issue: 733, P. 150683 - 150683

Published: Sept. 10, 2024

Language: Английский

Citations

4

Sirt1 overexpression inhibits chondrocyte ferroptosis via Ftl deacetylation to suppress the development of osteoarthritis DOI Creative Commons

Xiaolong Xiong,

Hui Huang, Ning Wang

et al.

Journal of Bone and Mineral Metabolism, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 9, 2025

Language: Английский

Citations

0

Potential role of SIRT1 in cell ferroptosis DOI Creative Commons
Yueming Zhang,

Fanxiao Kong,

Nan Li

et al.

Frontiers in Cell and Developmental Biology, Journal Year: 2025, Volume and Issue: 13

Published: March 5, 2025

Ferroptosis is a novel form of cell death that uniquely requires iron and characterized by accumulation, the generation free radicals leading to oxidative stress, formation lipid peroxides, which distinguish it from other forms death. The regulation ferroptosis extremely complex closely associated with spectrum diseases. Sirtuin 1 (SIRT1), NAD + -dependent histone deacetylase, has emerged as pivotal epigenetic regulator potential regulate through wide array genes intricately metabolism, homeostasis, glutathione biosynthesis, redox homeostasis. This review provides comprehensive overview specific mechanisms SIRT1 regulates explores its therapeutic value in context multiple disease pathologies, highlighting significance SIRT1-mediated treatment strategies.

Language: Английский

Citations

0

Ferroptosis in Arthritis: Driver of the Disease or Therapeutic Option? DOI Open Access

Shania Bieri,

Burkhard Möller, Jennifer Amsler

et al.

International Journal of Molecular Sciences, Journal Year: 2024, Volume and Issue: 25(15), P. 8212 - 8212

Published: July 27, 2024

Ferroptosis is a form of iron-dependent regulated cell death caused by the accumulation lipid peroxides. In this review, we summarize research on impact ferroptosis disease models and isolated cells in various types arthritis. While most studies have focused rheumatoid arthritis (RA) osteoarthritis (OA), there limited spondylarthritis crystal arthropathies. The effects inducing or inhibiting strongly depend studied type. search for new therapeutic targets, chondrocytes might promising any type On other hand, induction may also lead to desired decrease synovial fibroblasts RA. Thus, must consider cell-type-specific Further investigation needed clarify these complexities.

Language: Английский

Citations

3

Iron metabolism and arthritis: Exploring connections and therapeutic avenues DOI Creative Commons

Dachun Zhuo,

Wenze Xiao, Yu-Long Tang

et al.

Chinese Medical Journal, Journal Year: 2024, Volume and Issue: 137(14), P. 1651 - 1662

Published: June 12, 2024

Abstract Iron is indispensable for the viablility of nearly all living organisms, and it imperative cells, tissues, organisms to acquire this essential metal sufficiently maintain its metabolic stability survival. Disruption iron homeostasis can lead development various diseases. There a robust connection between metabolism infection, immunity, inflammation, aging, suggesting that disorders in may contribute pathogenesis arthritis. Numerous studies have focused on significant role arthritis potential targeted drug therapy. Targeting offers promising approach individualized treatment Therefore, review aimed investigate mechanisms by which body maintains impacts Furthermore, identify therapeutic targets active substances related metabolism, could provide research directions field.

Language: Английский

Citations

2

Pectolinarigenin targeting FGFR3 alleviates osteoarthritis progression by regulating the NF-κB/NLRP3 inflammasome pyroptotic pathway DOI

Peng Jiang,

Xiaonan Zhou,

Yue Yang

et al.

International Immunopharmacology, Journal Year: 2024, Volume and Issue: 140, P. 112741 - 112741

Published: Aug. 1, 2024

Language: Английский

Citations

1