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Neuronal cell-based high-throughput screen for enhancers of mitochondrial function reveals luteolin as a modulator of mitochondria-endoplasmic reticulum coupling.
Naia, Luana; Pinho, Catarina M; Dentoni, Giacomo; Liu, Jianping; Leal, Nuno Santos; Ferreira, Duarte M S; Schreiner, Bernadette; Filadi, Riccardo; Fão, Lígia; Connolly, Niamh M C; Forsell, Pontus; Nordvall, Gunnar; Shimozawa, Makoto; Greotti, Elisa; Basso, Emy; Theurey, Pierre; Gioran, Anna; Joselin, Alvin; Arsenian-Henriksson, Marie; Nilsson, Per; Rego, A Cristina; Ruas, Jorge L; Park, David; Bano, Daniele; Pizzo, Paola; Prehn, Jochen H M; Ankarcrona, Maria.
Afiliación
  • Naia L; Center for Alzheimer Research, Division of Neurogeriatrics, Department of Neurobiology Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden.
  • Pinho CM; Center for Alzheimer Research, Division of Neurogeriatrics, Department of Neurobiology Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden.
  • Dentoni G; Center for Alzheimer Research, Division of Neurogeriatrics, Department of Neurobiology Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden.
  • Liu J; Department of Medicine-Huddinge, Karolinska Institutet, Stockholm, Sweden.
  • Leal NS; Center for Alzheimer Research, Division of Neurogeriatrics, Department of Neurobiology Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden.
  • Ferreira DMS; Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
  • Schreiner B; Center for Alzheimer Research, Division of Neurogeriatrics, Department of Neurobiology Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden.
  • Filadi R; Department of Biomedical Sciences, University of Padua, Padua, Italy.
  • Fão L; Neuroscience Institute, National Research Council (CNR), 35131, Padua, Italy.
  • Connolly NMC; CNC-Center for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal.
  • Forsell P; Royal College of Surgeons in Ireland, Department of Physiology & Medical Physics Department, Dublin, Ireland.
  • Nordvall G; AlzeCure Pharma AB, Huddinge, Sweden.
  • Shimozawa M; AlzeCure Pharma AB, Huddinge, Sweden.
  • Greotti E; Center for Alzheimer Research, Division of Neurogeriatrics, Department of Neurobiology Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden.
  • Basso E; Department of Biomedical Sciences, University of Padua, Padua, Italy.
  • Theurey P; Neuroscience Institute, National Research Council (CNR), 35131, Padua, Italy.
  • Gioran A; Department of Biomedical Sciences, University of Padua, Padua, Italy.
  • Joselin A; Neuroscience Institute, National Research Council (CNR), 35131, Padua, Italy.
  • Arsenian-Henriksson M; Department of Biomedical Sciences, University of Padua, Padua, Italy.
  • Nilsson P; German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.
  • Rego AC; Department of Clinical Neurosciences, Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, Canada.
  • Ruas JL; Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
  • Park D; Center for Alzheimer Research, Division of Neurogeriatrics, Department of Neurobiology Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden.
  • Bano D; CNC-Center for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal.
  • Pizzo P; Faculty of Medicine, Institute of Biochemistry, University of Coimbra, Coimbra, Portugal.
  • Prehn JHM; Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
  • Ankarcrona M; Department of Clinical Neurosciences, Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, Canada.
BMC Biol ; 19(1): 57, 2021 03 24.
Article en En | MEDLINE | ID: mdl-33761951
BACKGROUND: Mitochondrial dysfunction is a common feature of aging, neurodegeneration, and metabolic diseases. Hence, mitotherapeutics may be valuable disease modifiers for a large number of conditions. In this study, we have set up a large-scale screening platform for mitochondrial-based modulators with promising therapeutic potential. RESULTS: Using differentiated human neuroblastoma cells, we screened 1200 FDA-approved compounds and identified 61 molecules that significantly increased cellular ATP without any cytotoxic effect. Following dose response curve-dependent selection, we identified the flavonoid luteolin as a primary hit. Further validation in neuronal models indicated that luteolin increased mitochondrial respiration in primary neurons, despite not affecting mitochondrial mass, structure, or mitochondria-derived reactive oxygen species. However, we found that luteolin increased contacts between mitochondria and endoplasmic reticulum (ER), contributing to increased mitochondrial calcium (Ca2+) and Ca2+-dependent pyruvate dehydrogenase activity. This signaling pathway likely contributed to the observed effect of luteolin on enhanced mitochondrial complexes I and II activities. Importantly, we observed that increased mitochondrial functions were dependent on the activity of ER Ca2+-releasing channels inositol 1,4,5-trisphosphate receptors (IP3Rs) both in neurons and in isolated synaptosomes. Additionally, luteolin treatment improved mitochondrial and locomotory activities in primary neurons and Caenorhabditis elegans expressing an expanded polyglutamine tract of the huntingtin protein. CONCLUSION: We provide a new screening platform for drug discovery validated in vitro and ex vivo. In addition, we describe a novel mechanism through which luteolin modulates mitochondrial activity in neuronal models with potential therapeutic validity for treatment of a variety of human diseases.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Luteolina / Retículo Endoplásmico / Mitocondrias / Neuronas Límite: Animals / Humans Idioma: En Revista: BMC Biol Asunto de la revista: BIOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Suecia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Luteolina / Retículo Endoplásmico / Mitocondrias / Neuronas Límite: Animals / Humans Idioma: En Revista: BMC Biol Asunto de la revista: BIOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Suecia
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