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Evaluating mitochondrial length, volume, and cristae ultrastructure in rare mouse adult stem cell populations

Since changes in mitochondrial morphology regulate key functions of stem cells, it is important to assess their structure under physiological and pathophysiological conditions. Here, we present techniques optimized in rare adult muscle stem cells (MuSCs). For evaluating mitochondrial length and volu...

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Detalles Bibliográficos
Autores principales: Triolo, Matthew, Wade, Steven, Baker, Nicole, Khacho, Mireille
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9943866/
https://www.ncbi.nlm.nih.gov/pubmed/36853728
http://dx.doi.org/10.1016/j.xpro.2023.102107
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author Triolo, Matthew
Wade, Steven
Baker, Nicole
Khacho, Mireille
author_facet Triolo, Matthew
Wade, Steven
Baker, Nicole
Khacho, Mireille
author_sort Triolo, Matthew
collection PubMed
description Since changes in mitochondrial morphology regulate key functions of stem cells, it is important to assess their structure under physiological and pathophysiological conditions. Here, we present techniques optimized in rare adult muscle stem cells (MuSCs). For evaluating mitochondrial length and volume within a compact cytoplasmic area in MuSCs on intact myofibers, we describe steps for mitochondrial staining, imaging, and quantification. For evaluating mitochondrial ultrastructure in small cell numbers, we describe steps for agarose embedding and quantification by TEM. For complete details on generation and use of this protocol, please refer to Baker et al. (2022).(1)
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spelling pubmed-99438662023-02-23 Evaluating mitochondrial length, volume, and cristae ultrastructure in rare mouse adult stem cell populations Triolo, Matthew Wade, Steven Baker, Nicole Khacho, Mireille STAR Protoc Protocol Since changes in mitochondrial morphology regulate key functions of stem cells, it is important to assess their structure under physiological and pathophysiological conditions. Here, we present techniques optimized in rare adult muscle stem cells (MuSCs). For evaluating mitochondrial length and volume within a compact cytoplasmic area in MuSCs on intact myofibers, we describe steps for mitochondrial staining, imaging, and quantification. For evaluating mitochondrial ultrastructure in small cell numbers, we describe steps for agarose embedding and quantification by TEM. For complete details on generation and use of this protocol, please refer to Baker et al. (2022).(1) Elsevier 2023-02-09 /pmc/articles/PMC9943866/ /pubmed/36853728 http://dx.doi.org/10.1016/j.xpro.2023.102107 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Triolo, Matthew
Wade, Steven
Baker, Nicole
Khacho, Mireille
Evaluating mitochondrial length, volume, and cristae ultrastructure in rare mouse adult stem cell populations
title Evaluating mitochondrial length, volume, and cristae ultrastructure in rare mouse adult stem cell populations
title_full Evaluating mitochondrial length, volume, and cristae ultrastructure in rare mouse adult stem cell populations
title_fullStr Evaluating mitochondrial length, volume, and cristae ultrastructure in rare mouse adult stem cell populations
title_full_unstemmed Evaluating mitochondrial length, volume, and cristae ultrastructure in rare mouse adult stem cell populations
title_short Evaluating mitochondrial length, volume, and cristae ultrastructure in rare mouse adult stem cell populations
title_sort evaluating mitochondrial length, volume, and cristae ultrastructure in rare mouse adult stem cell populations
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9943866/
https://www.ncbi.nlm.nih.gov/pubmed/36853728
http://dx.doi.org/10.1016/j.xpro.2023.102107
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