4.7 Editorial Material

Introduction to Special Issue on Mitochondrial Redox Signaling in Health and Disease

期刊

FREE RADICAL BIOLOGY AND MEDICINE
卷 100, 期 -, 页码 1-4

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.freeradbiomed.2016.08.004

关键词

-

资金

  1. BBSRC [BB/L020874/1] Funding Source: UKRI
  2. MRC [MC_U105663142] Funding Source: UKRI
  3. Biotechnology and Biological Sciences Research Council [BB/L020874/1] Funding Source: researchfish
  4. British Heart Foundation [PG/13/1/29801, FS/15/6/31298, FS/13/66/30445] Funding Source: researchfish
  5. Medical Research Council [MC_U105663142] Funding Source: researchfish
  6. Biotechnology and Biological Sciences Research Council [BB/L020874/1] Funding Source: Medline
  7. British Heart Foundation [FS/13/66/30445, FS/15/6/31298, PG/13/1/29801] Funding Source: Medline

向作者/读者索取更多资源

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Cell Biology

Defining roles of specific reactive oxygen species (ROS) in cell biology and physiology

Helmut Sies, Vsevolod V. Belousov, Navdeep S. Chandel, Michael J. Davies, Dean P. Jones, Giovanni E. Mann, Michael P. Murphy, Masayuki Yamamoto, Christine Winterbourn

Summary: This article discusses the key issues associated with identifying the physiological roles of oxidants, with a focus on H2O2 and O-2(.-). The article emphasizes the need for more precise measurement of oxidants and specific identification of their signaling targets. It also highlights the importance of inter-organellar communication and the contribution of environmental exposures. Development of tools for real-time detection and quantification of individual oxidants is crucial for achieving these goals.

NATURE REVIEWS MOLECULAR CELL BIOLOGY (2022)

Editorial Material Biochemistry & Molecular Biology

Special issue Extracellular Vesicles and Exosomes

Irving H. Zucker, Giovanni E. Mann, Pietro Ghezzi

FREE RADICAL BIOLOGY AND MEDICINE (2022)

Article Biochemistry & Molecular Biology

Hypothiocyanous Acid Disrupts the Barrier Function of Brain Endothelial Cells

Eveline van Leeuwen, Mark B. Hampton, Leon C. D. Smyth

Summary: Inflammation is a common feature in neurological diseases. This study demonstrates that a compound called hypothiocyanous acid can damage brain endothelial cells and result in the loss of barrier function, which may be a mechanism involved in neutrophil transmigration and neuroinflammation.

ANTIOXIDANTS (2022)

Article Biochemistry & Molecular Biology

A newly identified flavoprotein disulfide reductase Har protects Streptococcus pneumoniae against hypothiocyanous acid

Heather L. Shearer, Paul E. Pace, James C. Paton, Mark B. Hampton, Nina Dickerhof

Summary: This study reports the discovery of a previously unknown flavoprotein disulfide reductase with HOSCN reductase activity in HOSCN-tolerant Streptococcus pneumoniae, and demonstrates the role of this protein in combination with GSH utilization in protecting the bacteria from HOSCN.

JOURNAL OF BIOLOGICAL CHEMISTRY (2022)

Article Gastroenterology & Hepatology

Faecal Myeloperoxidase as a Biomarker of Endoscopic Activity in Inflammatory Bowel Disease

A. Swaminathan, G. M. Borichevsky, T. S. Edwards, E. Hirschfeld, T. C. Mules, C. M. Frampton, A. S. Day, M. B. Hampton, A. J. Kettle, R. B. Gearry

Summary: This study investigated the use of faecal myeloperoxidase (fMPO) as a biomarker for the activity of inflammatory bowel disease (IBD). The results showed that fMPO was significantly correlated with endoscopic activity and could accurately predict the severity and complexity of the disease.

JOURNAL OF CROHNS & COLITIS (2022)

Article Biochemistry & Molecular Biology

Site-specific decreases in DNA methylation in replicating cells following exposure to oxidative stress

Annika R. Seddon, Andrew B. Das, Mark B. Hampton, Aaron J. Stevens

Summary: Oxidative stress is a common feature of inflammation-driven cancers that modulates gene expression through the oxidation of transcription factors. Exposure to chloramines may result in decreased DNA methylation, leading to long-term impacts on cells, potentially affecting telomere length and cellular longevity.

HUMAN MOLECULAR GENETICS (2022)

Editorial Material Biochemistry & Molecular Biology

Introduction to Special Issue on Bench to bedside transition for pharmacological regulation of NRF2 in noncommunicable diseases

Antonio Cuadrado, Albena T. Dinkova-Kostova, Giovanni E. Mann

FREE RADICAL BIOLOGY AND MEDICINE (2023)

Review Immunology

Inside the phagosome: A bacterial perspective

Mark B. Hampton, Nina Dickerhof

Summary: The neutrophil phagosome poses a challenging environment for bacteria, but our understanding of the complex biochemistry within it is incomplete. Heterogeneity among phagosomes suggests that investigating the conditions that allow bacteria to survive could lead to new therapeutic strategies. Monitoring or recovering bacteria from phagosomes and unbiased screening for essential bacterial genes are important for gaining insights into their survival mechanisms inside neutrophil phagosomes.

IMMUNOLOGICAL REVIEWS (2023)

Review Biochemistry & Molecular Biology

Stress Activated MAP Kinases and Cyclin-Dependent Kinase 5 Mediate Nuclear Translocation of Nrf2 via Hsp90α-Pin1-Dynein Motor Transport Machinery

Tetsuro Ishii, Eiji Warabi, Giovanni E. Mann

Summary: Low levels of oxidative stress activate Nrf2, which is a transcription factor that regulates genes involved in detoxification and defense against oxidative damage. MAP kinases p38, ERK, and JNK cooperate in the nuclear accumulation of Nrf2. Membrane trafficking and phosphorylation of Nrf2 by ceramide and PKC zeta stabilize Nrf2 and prevent nuclear export. ERK and JNK phosphorylation of Nrf2 promote its association with Pin1 and importin-alpha 5, facilitating nuclear translocation. Pin1-Hsp90 alpha complex and dynein motor complex transport Nrf2 to the nucleus along microtubules. This pathway is also involved in the transport of other proteins, such as pyruvate kinase M2 and hypoxia-inducible transcription factor-1, and may be a potential therapeutic target for tumors.

ANTIOXIDANTS (2023)

Editorial Material Biochemistry & Molecular Biology

The mitochondrial ATP synthase as an ATP consumer-a surprising therapeutic target

Gabriel E. Valdebenito, Anitta R. Chacko, Michael R. Duchen

Summary: The mitochondrial F1Fo-ATP synthase can both synthesize ATP and pump protons, with potential implications for diseases. In a recent study, Acin-Perez et al. identified (+)-epicatechin as a compound that selectively inhibits ATP hydrolysis without affecting ATP synthesis. They found that this compound has significant benefits for cell and tissue function in disease models, suggesting a novel therapeutic approach for mitochondrial disease.

EMBO JOURNAL (2023)

Article Biochemistry & Molecular Biology

MerA functions as a hypothiocyanous acid reductase and defense mechanism in Staphylococcus aureus

Heather L. Shearer, Vu V. Loi, Paul Weiland, Gert Bange, Florian Altegoer, Mark B. Hampton, Haike Antelmann, Nina Dickerhof

Summary: A study reveals that Staphylococcus aureus has developed a defense mechanism against the antimicrobial oxidant hypothiocyanous acid (HOSCN) in order to cause infections in humans. The enzyme MerA acts as a HOSCN reductase, protecting the bacteria from oxidative stress. Understanding the structure and function of MerA may lead to new strategies for treating S. aureus infections.

MOLECULAR MICROBIOLOGY (2023)

Article Biochemistry & Molecular Biology

Redox and metal profiles in human coronary endothelial and smooth muscle cells under hyperoxia, physiological normoxia and hypoxia: Effects of NRF2 signaling on intracellular zinc

Matthew J. Smith, Fan Yang, Alexander Griffiths, Alexander Morrell, Sarah J. Chapple, Richard C. M. Siow, Theodora Stewart, Wolfgang Maret, Giovanni E. Mann

Summary: Zinc is vital for cellular antioxidant defenses and imbalanced zinc homeostasis increases the risk of coronary heart disease and ischemia/reperfusion injury. In human coronary artery cells, the total intracellular zinc content decreases significantly when oxygen levels are lowered. This is accompanied by differences in redox phenotype and metal profiles, indicating the involvement of NRF2 signaling in zinc regulation.

REDOX BIOLOGY (2023)

Review Microbiology

Control of Redox Homeostasis by Short-Chain Fatty Acids: Implications for the Prevention and Treatment of Breast Cancer

Carmen Gonzalez-Bosch, Patricia A. Zunszain, Giovanni E. Mann

Summary: Breast cancer is a major cause of death in women worldwide, and there is a need for new alternative therapies. Plant-derived compounds, such as flavonoids and polyphenols, have gained increasing interest for their antioxidant properties and ability to regulate cell homeostasis. Short-chain fatty acids (SCFAs), produced by intestinal microbiota and obtained from the diet, also play a crucial role in redox signaling and cancer prevention. This review focuses on the antioxidant properties of SCFAs and their impact on breast cancer development and treatment.

PATHOGENS (2023)

Article Microbiology

Identification of Streptococcus pneumoniae genes associated with hypothiocyanous acid tolerance through genome-wide screening

Heather L. Shearer, Paul E. Pace, Leah M. Smith, Peter C. Fineran, Allison J. Matthews, Andrew Camilli, Nina Dickerhof, Mark B. Hampton

Summary: By using saturation transposon mutagenesis and deep sequencing, this study identified 37 genes associated with hypothiocyanous acid (HOSCN) tolerance in Streptococcus pneumoniae. These genes are involved in metabolism, membrane transport, DNA repair, and oxidant detoxification. Validation experiments showed that most of the single-gene deletion mutants exhibited increased sensitivity to HOSCN, and some mutants showed enhanced activity of antioxidant defense systems. The double deletion of glutathione reductase and sodA significantly sensitized the bacteria. The HOSCN defense systems identified in this study may serve as viable targets for novel therapeutics against S. pneumoniae.

JOURNAL OF BACTERIOLOGY (2023)

Article Biochemistry & Molecular Biology

Vascular protection afforded by zinc supplementation in human coronary artery smooth muscle cells mediated by NRF2 signaling under hypoxia/ reoxygenation

Fan Yang, Matthew J. Smith, Alexander Griffiths, Alexander Morrell, Sarah J. Chapple, Richard C. M. Siow, Theodora Stewart, Wolfgang Maret, Giovanni E. Mann

Summary: Zinc has various beneficial effects on human coronary artery smooth muscle cells, including antioxidant, anti-inflammatory, and anti-proliferative actions. The supplementation of zinc increases the total intracellular zinc content and enhances the NRF2 signaling pathway, providing protection against oxidative stress. These effects are more pronounced under high oxygen tension compared to normal oxygen conditions.

REDOX BIOLOGY (2023)

Correction Biochemistry & Molecular Biology

miR-196a provides antioxidative neuroprotection via USP15/Nrf2 regulation in Huntington's disease (vol 209, pg 292, 2023)

Siew Chin Chan, Chih-Wei Tung, Chia-Wei Lin, Yun-Shiuan Tung, Po-Min Wu, Pei-Hsun Cheng, Chuan-Mu Chen, Shang-Hsun Yang

FREE RADICAL BIOLOGY AND MEDICINE (2024)

Article Biochemistry & Molecular Biology

Ribosome-targeting antibiotic control NLRP3-mediated inflammation by inhibiting mitochondrial DNA synthesis

Suyuan Liu, Meiling Tan, Jiangxue Cai, Chenxuan Li, Miaoxin Yang, Xiaoxiao Sun, Bin He

Summary: This study reveals that the antibiotic doxycycline effectively inhibits NLRP3 inflammasome activation by targeting mitochondrial translation and mtDNA synthesis, offering potential for the treatment of NLRP3-related diseases.

FREE RADICAL BIOLOGY AND MEDICINE (2024)

Article Biochemistry & Molecular Biology

Protectin D1 inhibits TLR4 signaling pathway to alleviate non-alcoholic steatohepatitis via upregulating IRAK-M

Hao Liu, Nana Li, Ge Kuang, Xia Gong, Ting Wang, Jun Hu, Hui Du, Minxuan Zhong, Jiashi Guo, Yao Xie, Yang Xiang, Shengwang Wu, Yiling Yuan, Xinru Yin, Jingyuan Wan, Ke Li

Summary: Protectin D1 (PTD1) improves hepatic steatosis, inflammation and fibrosis in a NASH mouse model by inhibiting the activation of TLR4 downstream signaling pathway, possibly through upregulation of IRAK-M expression, suggesting a potential new treatment for NASH.

FREE RADICAL BIOLOGY AND MEDICINE (2024)