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X-WR-CALNAME:Bordeaux Neurocampus
X-ORIGINAL-URL:https://www.bordeaux-neurocampus.fr
X-WR-CALDESC:Évènements pour Bordeaux Neurocampus
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DTSTART:20260329T010000
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DTSTART;TZID=Europe/Paris:20260318T113000
DTEND;TZID=Europe/Paris:20260318T113000
DTSTAMP:20260406T052318
CREATED:20260218T130530Z
LAST-MODIFIED:20260316T143012Z
UID:194544-1773833400-1773833400@www.bordeaux-neurocampus.fr
SUMMARY:Seminar - Anthonny Grillo
DESCRIPTION:Venue: Centre Broca \n\nAnthonny S. Grillo\nDepartment of Chemistry – Chair\, Biochemistry Division\nUniv. Cincinnati\, USA\nhttps://www.grillolabuc.com/ \nTitle \nA mitochondrial Complex I deficiency induces iron accumulation and tau aggregation. \nAbstract \nMitochondrial bioenergetic deficiencies are one of the earliest features of most age-related diseases such as Alzheimer’s disease\, Parkinson’s disease\, and ALS. Despite its pervasive recognition as a hallmark of these neurodegenerative diseases\, there remains an urgent need to understand the multivariate influences mitochondrial dysfunction has on the molecular determinants that elicit biologic decline. We and others hypothesize age-related reductions in the Electron Transport Chain\nactivity cause metabolic O2 imbalances or iron accumulation that is associated with neuroinflammation in dementia and movement disorders. We discovered mice missing mitochondrial Complex I show O2-dependent accumulation of tau\, and that housing mice in low oxygen environments can prevent tau pathogenicity. Further\, Complex I deficiencies induce the\naccumulation and misregulation of iron to drive inflammation. Collectively\, this work suggests mitochondrial Complex I deficiencies may induce the pathogenic accumulation of proteins or metals involved in tauopathies with Parkinsonism-like features such as Progressive Supranuclear Palsy. \nBiography: \nDr. Grillo was born in Michigan\, USA before obtaining a B.S. in Biochemistry and a B.S. in Chemistry from the University of Michigan. He began graduate studies in Marty Burke’s Lab at the University of Illinois at Urbana-Champaign as an NSF Predoctoral Fellow (NSF GRFP) and obtained his Ph.D. with a focus on Chemical Biology in 2017. His thesis centered on the discovery\, development\, and mechanistic understanding of small molecules that mimic protein function to restore physiology to protein-deficient organisms\, thereby acting as prostheses on the molecular scale. As an NRSA Postdoctoral Fellow and Alzheimer’s Disease Research Center Trainee in Matt Kaeberlein’s Lab at the University of Washington\, Dr. Grillo elucidated the role of protein kinase C in promoting neuroinflammation in mice missing Complex I of the Electron Transport Chain and probed the etiology of mitochondrial dysfunction in tauopathies and movement disorders. He joined the University of Cincinnati Department of Chemistry (Biochemistry Division) in 2022 as an Assistant Professor. Interdisciplinary research in the Grillo Lab centers on revealing how mitochondrial dysfunction alters micronutrient metabolism (e.g. metals\, branched chain amino\nacids\, oxygen\, vitamins\, etc.) to elicit neurodegeneration in movement disorders and other neurometabolic diseases. \n  \n
URL:https://www.bordeaux-neurocampus.fr/event/seminar-anthonny-grillo/
CATEGORIES:A la une,Pour les scientifiques,Séminaire Impromptu
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