Utilize este identificador para referenciar este registo:
https://hdl.handle.net/10316/103784
Título: | Neuronal cell-based high-throughput screen for enhancers of mitochondrial function reveals luteolin as a modulator of mitochondria-endoplasmic reticulum coupling | Autor: | Naia, Luana Carvalho 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 |
Palavras-chave: | High-throughput screen; Mitochondria; Luteolin; Mitochondria-ER contacts; Mitochondrial calcium | Data: | 24-Mar-2021 | Editora: | Springer Nature | Projeto: | Marie Skłodowska-Curie | Título da revista, periódico, livro ou evento: | BMC Biology | Volume: | 19 | Número: | 1 | Resumo: | 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. | URI: | https://hdl.handle.net/10316/103784 | ISSN: | 1741-7007 | DOI: | 10.1186/s12915-021-00979-5 | Direitos: | openAccess |
Aparece nas coleções: | I&D CNC - Artigos em Revistas Internacionais FMUC Medicina - Artigos em Revistas Internacionais |
Ficheiros deste registo:
Ficheiro | Descrição | Tamanho | Formato | |
---|---|---|---|---|
s12915-021-00979-5.pdf | 6.96 MB | Adobe PDF | Ver/Abrir |
Citações SCOPUSTM
26
Visto em 4/nov/2024
Citações WEB OF SCIENCETM
23
Visto em 2/nov/2024
Visualizações de página
102
Visto em 5/nov/2024
Downloads
45
Visto em 5/nov/2024
Google ScholarTM
Verificar
Altmetric
Altmetric
Este registo está protegido por Licença Creative Commons