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Mitochondrial reactive oxygen species and inflammation: Molecular mechanisms,diseases and promising therapies
Institution:1. Department of Physical Therapy, Faculty of Health Sciences, Ariel University, Ariel, Israel;2. Åstrand Laboratory, The Swedish School of Sport and Health Sciences, GIH, Stockholm, Sweden;3. Department of Neurology, The Agnes Ginges Center for Human Neurogenetics, Hadassah – Hebrew University Medical Center, Jerusalem, Israel;1. Lowell Observatory, Flagstaff, AZ, United States of America;2. NASA Goddard Space Flight Center, Greenbelt, MD, United States of America;3. Southwest Research Institute, Boulder, CO, United States of America;4. Planetary Science Institute, Tucson, AZ, United States of America;5. Brigham Young University, Provo, UT, United States of America;6. Gemini Observatory/AURA, Santiago, Chile
Abstract:Over the last few decades, many different groups have been engaged in studies of new roles for mitochondria, particularly the coupling of alterations in the redox pathway with the inflammatory responses involved in different diseases, including Alzheimer’s disease, Parkinson's disease, atherosclerosis, cerebral cavernous malformations, cystic fibrosis and cancer. Mitochondrial dysfunction is important in these pathological conditions, suggesting a pivotal role for mitochondria in the coordination of pro-inflammatory signaling from the cytosol and signaling from other subcellular organelles. In this regard, mitochondrial reactive oxygen species are emerging as perfect liaisons that can trigger the assembly and successive activation of large caspase-1- activating complexes known as inflammasomes. This review offers a glimpse into the mechanisms by which inflammasomes are activated by mitochondrial mechanisms, including reactive oxygen species production and mitochondrial Ca2+ uptake, and the roles they can play in several inflammatory pathologies.
Keywords:Mitochondrial dysfunction  Inflammatory response  ROS  Inflammasome  Inflammation-related diseases
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