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Local mitochondrial replication in the periphery of neurons requires the eEF1A1 protein and thetranslation of nuclear-encoded proteins.
Cardanho-Ramos, Carlos; Simões, Rúben Alves; Wang, Yi-Zhi; Faria-Pereira, Andreia; Bomba-Warczak, Ewa; Craessaerts, Katleen; Spinazzi, Marco; Savas, Jeffrey N; Morais, Vanessa A.
Afiliação
  • Cardanho-Ramos C; Instituto de Medicina Molecular-João Lobo Antunes, Faculdade de Medicina, Universidade de Lisboa, Lisboa, Portugal.
  • Simões RA; Instituto de Medicina Molecular-João Lobo Antunes, Faculdade de Medicina, Universidade de Lisboa, Lisboa, Portugal.
  • Wang YZ; Department of Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.
  • Faria-Pereira A; Instituto de Medicina Molecular-João Lobo Antunes, Faculdade de Medicina, Universidade de Lisboa, Lisboa, Portugal.
  • Bomba-Warczak E; Department of Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.
  • Craessaerts K; VIB Center for Brain and Disease Research and KU Leuven, Department of Neurosciences, Leuven, Belgium.
  • Spinazzi M; Dementia Research Institute, University College London, London, UK.
  • Savas JN; VIB Center for Brain and Disease Research and KU Leuven, Department of Neurosciences, Leuven, Belgium.
  • Morais VA; Dementia Research Institute, University College London, London, UK.
iScience ; 27(4): 109136, 2024 Apr 19.
Article em En | MEDLINE | ID: mdl-38510136
ABSTRACT
In neurons, it is commonly assumed that mitochondrial replication only occurs in the cell body, after which the mitochondria must travel to the neuron's periphery. However, while mitochondrial DNA replication has been observed to occur away from the cell body, the specific mechanisms involved remain elusive. Using EdU-labelling in mouse primary neurons, we developed a tool to determine the mitochondrial replication rate. Taking of advantage of microfluidic devices, we confirmed that mitochondrial replication also occurs locally in the periphery of neurons. To achieve this, mitochondria require de novo nuclear-encoded, but not mitochondrial-encoded protein translation. Following a proteomic screen comparing synaptic with non-synaptic mitochondria, we identified two elongation factors - eEF1A1 and TUFM - that were upregulated in synaptic mitochondria. We found that mitochondrial replication is impaired upon the downregulation of eEF1A1, and this is particularly relevant in the periphery of neurons.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: IScience Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Portugal

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: IScience Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Portugal