BCL6 Promotes Transcription of GPR61 to Suppress IL‐1β‐Induced Osteoarthritis Progression in C28/I2 Cells DOI

Guangxuan Zeng,

Yizhou Xu, Zhengnan Li

и другие.

Microbiology and Immunology, Год журнала: 2024, Номер unknown

Опубликована: Дек. 23, 2024

Abstract Osteoarthritis (OA) is the most common joint disease and its pathogenic mechanism remains to be ensured. This study focused on regulatory relation between B‐cell lymphoma 6 (BCL6) G‐protein‐coupled receptor 61 (GPR61) underlying IL‐1β in OA. Real‐time quantitative polymerase chain reaction western blot were performed for mRNA protein detection. Oxidative injury was assessed by reactive oxygen species (ROS), malondialdehyde (MDA), glutathione (GSH) via kits. Fe 2+ level measured an iron assay kit. Relation analysis BCL6 GPR61 implemented employing ChIP dual‐luciferase reporter assay. downregulated OA samples IL‐1β‐induced C28/I2 cells. cell inflammation, extracellular matrix (ECM) degradation, oxidative stress, ferroptosis all returned overexpression of GPR61. downregulation detected patients IL‐1β‐exposed could promote transcription suppressed progression upregulating The BCL6/GPR61 axis activated PKA/CREB pathway IL‐1β‐treated above results suggested that mitigated induced enhancing BCL6/GPR61/PKA/CREB may considered as a novel OA, has potential act target

Язык: Английский

Sappanone A attenuates rheumatoid arthritis via inhibiting PI3K/AKT/NF-κB and JAK2/STAT3 signaling pathways in vivo and in vitro DOI

Chengjie Deng,

Shiqin Sun,

Huaxi Zhang

и другие.

International Immunopharmacology, Год журнала: 2024, Номер 143, С. 113560 - 113560

Опубликована: Ноя. 12, 2024

Язык: Английский

Процитировано

4

Relaxin‐2 Alleviated Ferroptosis and Inflammation in TNF‐α‐Treated Chondrocytes via Regulating the Nrf2/NFκB Signaling Pathway DOI Open Access
Yuwei Fan, Ya‐Zhou He, Da Ma

и другие.

Peptide Science, Год журнала: 2025, Номер 117(2)

Опубликована: Янв. 25, 2025

ABSTRACT Excessive inflammatory responses and ferroptosis‐associated dysfunction of chondrocytes are significant pathological features osteoarthritis (OA). Relaxin‐2, a well‐known hormone involved in metabolic regulation across various tissues cells, has not been extensively studied the context chondrocyte OA. T/C‐28a2 cells were stimulated with tumor necrosis factor α (TNF‐α) (10 ng/mL) or without recombinant human relaxin‐2 (rh relaxin‐2) (25, 50 nM) for 48 h. Various techniques, including 2′,7′‐dichlorodihydrofluorescein diacetate (DCFH‐DA) staining, real‐time PCR, western blot analysis, enzyme‐linked immunosorbent assay (ELISA), luciferase activity assays, employed. We discovered that exposure to TNF‐α decreased expression Relaxin‐2 at both mRNA protein levels. Further investigation revealed treatment rh mitigated lipid peroxidation by reducing levels reactive oxygen species (ROS), malondialdehyde (MDA), 4‐hydroxy‐2‐nonenal (4‐HNE), while increasing superoxide dismutase (SOD) glutathione (GSH) content. Notably, restored iron metabolism balance disrupted decreasing Fe 2+ levels, downregulating transferrin receptor 1 (TFR1) gene expression, upregulating ferritin expression. Additionally, alleviated ferroptosis induced these peroxidase 4 (GPX4) acyl‐CoA synthetase long‐chain family member (ACSL4) lactate dehydrogenase (LDH) release. Rh also inhibited TNF‐α‐induced pro‐inflammatory cytokines, interleukin‐1β (IL‐1β) interleukin‐6 (IL‐6). Interestingly, attenuated degeneration suppressing matrix metalloproteinase‐13 (MMP‐13) preventing degradation collagen type II alpha1 chain (Col2α). Mechanistically, effects found be mediated through nuclear erythroid 2‐related 2 (Nrf2)/NF‐κB signaling pathway. Our findings suggest could potential therapeutic strategy

Язык: Английский

Процитировано

0

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

Fanxiao Kong,

Nan Li

и другие.

Frontiers in Cell and Developmental Biology, Год журнала: 2025, Номер 13

Опубликована: Март 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.

Язык: Английский

Процитировано

0

Research advances of Sappanone A in inflammation-related diseases DOI Creative Commons
Jie Fu, Chen Xiu, Jinglun Li

и другие.

Frontiers in Medicine, Год журнала: 2025, Номер 12

Опубликована: Май 8, 2025

Sappanone A (SA), a kind of homoisoflavanone extracted from the dry heartwood Caesalpinia sappan L., has been shown to possess diverse bioactivities involving anti-inflammatory, antioxidant, and anti-apoptotic properties. Sustained proinflammatory state is major factor in occurrence development various diseases. Given characteristics SA, many studies have explored effect SA on inflammation-related diseases, which uncovered multifaceted therapeutic potential such In this mini-review, we summarized current achievements diseases (such as myocardial ischemia-reperfusion injury, liver respiratory kidney etc.), order provide useful insights into role benefit future clinical applications.

Язык: Английский

Процитировано

0

Mechanisms and Therapeutic Potential of GPX4 in Pain Modulation DOI Creative Commons

Shiwen Fan,

Kaixin Wang, Tianhao Zhang

и другие.

Pain and Therapy, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 6, 2024

Pain, a complex symptom encompassing both sensory and emotional dimensions, constitutes significant global public health issue. Oxidative stress is pivotal factor in the pathophysiology of pain, with glutathione peroxidase 4 (GPX4) recognized as crucial antioxidant enzyme involved defense mechanisms ferroptosis pathways. This review systematically explores GPX4's functions across various pain models, including neuropathic, inflammatory, low back, cancer-related pain. Specifically, focus includes physiological roles, mechanisms, regulation ferroptosis, involvement signal transduction pathways, metabolic regulation. By summarizing current research, we highlight potential GPX4-targeted therapies management.

Язык: Английский

Процитировано

2

BCL6 Promotes Transcription of GPR61 to Suppress IL‐1β‐Induced Osteoarthritis Progression in C28/I2 Cells DOI

Guangxuan Zeng,

Yizhou Xu, Zhengnan Li

и другие.

Microbiology and Immunology, Год журнала: 2024, Номер unknown

Опубликована: Дек. 23, 2024

Abstract Osteoarthritis (OA) is the most common joint disease and its pathogenic mechanism remains to be ensured. This study focused on regulatory relation between B‐cell lymphoma 6 (BCL6) G‐protein‐coupled receptor 61 (GPR61) underlying IL‐1β in OA. Real‐time quantitative polymerase chain reaction western blot were performed for mRNA protein detection. Oxidative injury was assessed by reactive oxygen species (ROS), malondialdehyde (MDA), glutathione (GSH) via kits. Fe 2+ level measured an iron assay kit. Relation analysis BCL6 GPR61 implemented employing ChIP dual‐luciferase reporter assay. downregulated OA samples IL‐1β‐induced C28/I2 cells. cell inflammation, extracellular matrix (ECM) degradation, oxidative stress, ferroptosis all returned overexpression of GPR61. downregulation detected patients IL‐1β‐exposed could promote transcription suppressed progression upregulating The BCL6/GPR61 axis activated PKA/CREB pathway IL‐1β‐treated above results suggested that mitigated induced enhancing BCL6/GPR61/PKA/CREB may considered as a novel OA, has potential act target

Язык: Английский

Процитировано

0