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Suppressing Ferroptosis Decreases the Multiplication of Mycobacterium Marinum in Human Macrophages

https://doi.org/10.2139/ssrn.4352898
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Sixty-three Cases of Mycobacterium marinum Infection
inferredcites →https://doi.org/10.1007/s13238-020-00789-5openalex-extracted
Cystine transporter SLC7A11/xCT in cancer: ferroptosis, nutrient dependency, and cancer therapy
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Autophagy Is a Defense Mechanism Inhibiting BCG and Mycobacterium tuberculosis Survival in Infected Macrophages
inferredcites →https://doi.org/10.1016/j.cell.2012.03.042openalex-extracted
Ferroptosis: An Iron-Dependent Form of Nonapoptotic Cell Death
inferredcites →https://doi.org/10.1016/j.diagmicrobio.2011.07.003openalex-extracted
Outbreak of a cutaneous Mycobacterium marinum infection in Jiangsu Haian, China
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2020.02.027openalex-extracted
Lipid peroxidation and ferroptosis: The role of GSH and GPx4
inferredcites →https://doi.org/10.1016/j.micinf.2004.10.003openalex-extracted
Mycobacterium marinum: the generalization and specialization of a pathogenic mycobacterium
inferredcites →https://doi.org/10.1038/nchembio.2239openalex-extracted
ACSL4 dictates ferroptosis sensitivity by shaping cellular lipid composition
inferredcites →https://doi.org/10.1038/s41419-020-2298-2openalex-extracted
Ferroptosis: past, present and future
inferredcites →https://doi.org/10.1080/10715762.2021.1876856openalex-extracted
Ferroptosis and cardiovascular disease: role of free radical-induced lipid peroxidation
inferredcites →https://doi.org/10.1084/jem.20140857openalex-extracted
T cell lipid peroxidation induces ferroptosis and prevents immunity to infection
inferredcites →https://doi.org/10.1084/jem.20181776openalex-extracted
A major role for ferroptosis in Mycobacterium tuberculosis –induced cell death and tissue necrosis
inferredcites →https://doi.org/10.1086/376628openalex-extracted
Fish Tank Exposure and Cutaneous Infections Due to Mycobacterium marinum: Tuberculin Skin Testing, Treatment, and Prevention
inferredcites →https://doi.org/10.1086/598928openalex-extracted
Sequelae of World War II: An Outbreak of Chronic Cutaneous Nontuberculous Mycobacterial Infection among Satowanese Islanders
inferredcites →https://doi.org/10.1111/imm.12587openalex-extracted
Autophagy is involved in regulating the immune response of dendritic cells to influenza A (H1N1) pdm09 infection
inferredcites →https://doi.org/10.1111/j.1468-3083.2010.03684.xopenalex-extracted
Cutaneous non-tuberculous Mycobacterial infections: a clinical and histopathological study of 17 cases from Lebanon
inferredcites →https://doi.org/10.1126/science.1103966openalex-extracted
Autophagy Defends Cells Against Invading Group A Streptococcus
inferredcites →https://doi.org/10.1126/science.1106036openalex-extracted
Escape of Intracellular Shigella from Autophagy
inferredcites →https://doi.org/10.1164/rccm.200604-571stopenalex-extracted
An Official ATS/IDSA Statement: Diagnosis, Treatment, and Prevention of Nontuberculous Mycobacterial Diseases
inferredcites →https://doi.org/10.1172/jci99490openalex-extracted
Pseudomonas aeruginosa utilizes host polyunsaturated phosphatidylethanolamines to trigger theft-ferroptosis in bronchial epithelium
inferredcites →https://doi.org/10.3389/fimmu.2012.00043openalex-extracted
Autophagosomal Protein Dynamics and Influenza Virus Infection
inferredcites →https://doi.org/10.3390/cancers12010164openalex-extracted
Ferroptosis in Cancer Cell Biology
inferredcites →https://doi.org/10.4161/auto.4450openalex-extracted
Listeria monocytogenesEvades Killing by Autophagy During Colonization of Host Cells
inferredcites →https://doi.org/10.5812/ircmj.10120openalex-extracted
Review of Mycobacterium marinum Infection Reported From Iran and Report of Three New Cases With Sporotrichoid Presentation
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