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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
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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 |
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author | Faitg, Julie Lacefield, Clay Davey, Tracey White, Kathryn Laws, Ross Kosmidis, Stylianos Reeve, Amy K. Kandel, Eric R. Vincent, Amy E. Picard, Martin |
author_facet | Faitg, Julie Lacefield, Clay Davey, Tracey White, Kathryn Laws, Ross Kosmidis, Stylianos Reeve, Amy K. Kandel, Eric R. Vincent, Amy E. Picard, Martin |
author_sort | Faitg, Julie |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8423436 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
spelling | pubmed-84234362021-09-07 3D neuronal mitochondrial morphology in axons, dendrites, and somata of the aging mouse hippocampus Faitg, Julie Lacefield, Clay Davey, Tracey White, Kathryn Laws, Ross Kosmidis, Stylianos Reeve, Amy K. Kandel, Eric R. Vincent, Amy E. Picard, Martin Cell Rep Article 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. 2021-08-10 /pmc/articles/PMC8423436/ /pubmed/34380033 http://dx.doi.org/10.1016/j.celrep.2021.109509 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY 4.0 license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Article Faitg, Julie Lacefield, Clay Davey, Tracey White, Kathryn Laws, Ross Kosmidis, Stylianos Reeve, Amy K. Kandel, Eric R. Vincent, Amy E. Picard, Martin 3D neuronal mitochondrial morphology in axons, dendrites, and somata of the aging mouse hippocampus |
title | 3D neuronal mitochondrial morphology in axons, dendrites, and somata
of the aging mouse hippocampus |
title_full | 3D neuronal mitochondrial morphology in axons, dendrites, and somata
of the aging mouse hippocampus |
title_fullStr | 3D neuronal mitochondrial morphology in axons, dendrites, and somata
of the aging mouse hippocampus |
title_full_unstemmed | 3D neuronal mitochondrial morphology in axons, dendrites, and somata
of the aging mouse hippocampus |
title_short | 3D neuronal mitochondrial morphology in axons, dendrites, and somata
of the aging mouse hippocampus |
title_sort | 3d neuronal mitochondrial morphology in axons, dendrites, and somata
of the aging mouse hippocampus |
topic | Article |
url | 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 |
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