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3D neuronal mitochondrial morphology in axons, dendrites, and somata of the aging mouse hippocampus

The brain’s ability to process complex information relies on the constant supply of energy through aerobic respiration by mitochondria. Neurons contain three anatomically distinct compartments—the soma, dendrites, and projecting axons—which have different energetic and biochemical requirements, as w...

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Detalles Bibliográficos
Autores principales: Faitg, Julie, Lacefield, Clay, Davey, Tracey, White, Kathryn, Laws, Ross, Kosmidis, Stylianos, Reeve, Amy K., Kandel, Eric R., Vincent, Amy E., Picard, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8423436/
https://www.ncbi.nlm.nih.gov/pubmed/34380033
http://dx.doi.org/10.1016/j.celrep.2021.109509
Descripción
Sumario:The brain’s ability to process complex information relies on the constant supply of energy through aerobic respiration by mitochondria. Neurons contain three anatomically distinct compartments—the soma, dendrites, and projecting axons—which have different energetic and biochemical requirements, as well as different mitochondrial morphologies in cultured systems. In this study, we apply quantitative three-dimensional electron microscopy to map mitochondrial network morphology and complexity in the mouse brain. We examine somatic, dendritic, and axonal mitochondria in the dentate gyrus and cornu ammonis 1 (CA1) of the mouse hippocampus, two subregions with distinct principal cell types and functions. We also establish compartment-specific differences in mitochondrial morphology across these cell types between young and old mice, highlighting differences in age-related morphological recalibrations. Overall, these data define the nature of the neuronal mitochondrial network in the mouse hippocampus, providing a foundation to examine the role of mitochondrial morpho-function in the aging brain.