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Cell metabolism sets the differences between subpopulations of satellite cells (SCs)
BACKGROUND: We have recently characterized two distinct populations of Satellite Cells (SCs) that differ in proliferation, regenerative potential, and mitochondrial coupling efficiency and classified these in Low Proliferative Clones (LPC) and High Proliferative Clones (HPC). Herewith, we have inves...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3689622/ https://www.ncbi.nlm.nih.gov/pubmed/23641781 http://dx.doi.org/10.1186/1471-2121-14-24 |
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author | Repele, Andrea Lupi, Ramona Eaton, Simon Urbani, Luca De Coppi, Paolo Campanella, Michelangelo |
author_facet | Repele, Andrea Lupi, Ramona Eaton, Simon Urbani, Luca De Coppi, Paolo Campanella, Michelangelo |
author_sort | Repele, Andrea |
collection | PubMed |
description | BACKGROUND: We have recently characterized two distinct populations of Satellite Cells (SCs) that differ in proliferation, regenerative potential, and mitochondrial coupling efficiency and classified these in Low Proliferative Clones (LPC) and High Proliferative Clones (HPC). Herewith, we have investigated their cell metabolism and individuated features that remark an intrinsic difference in basal physiology but that are retrievable also at the initial phases of their cloning. RESULTS: Indeed, LPC and HPC can be distinguished for mitochondrial membrane potential (ΔΨ(m)) just after isolation from the fiber. This is matched by mitochondrial redox state measured via NAD(+)/NADH analysis and alternative respiratory CO(2) production in cloned cells. All these parameters are accountable for metabolic differences reflected indeed by alternative expression of the glycolytic enzyme 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 (Pfkfb3). Also Ca(2+) handling by mitochondria is different together with the sensitivity to apoptosis triggered via this pathway. Finally, according to the above, we were able to determine which one among the clones represents the suitable stem cell. CONCLUSIONS: These experimental observations report novel physiological features in the cell biology of SCs and refer to an intrinsic heterogeneity within which their stemness may reside. |
format | Online Article Text |
id | pubmed-3689622 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36896222013-06-22 Cell metabolism sets the differences between subpopulations of satellite cells (SCs) Repele, Andrea Lupi, Ramona Eaton, Simon Urbani, Luca De Coppi, Paolo Campanella, Michelangelo BMC Cell Biol Research Article BACKGROUND: We have recently characterized two distinct populations of Satellite Cells (SCs) that differ in proliferation, regenerative potential, and mitochondrial coupling efficiency and classified these in Low Proliferative Clones (LPC) and High Proliferative Clones (HPC). Herewith, we have investigated their cell metabolism and individuated features that remark an intrinsic difference in basal physiology but that are retrievable also at the initial phases of their cloning. RESULTS: Indeed, LPC and HPC can be distinguished for mitochondrial membrane potential (ΔΨ(m)) just after isolation from the fiber. This is matched by mitochondrial redox state measured via NAD(+)/NADH analysis and alternative respiratory CO(2) production in cloned cells. All these parameters are accountable for metabolic differences reflected indeed by alternative expression of the glycolytic enzyme 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 (Pfkfb3). Also Ca(2+) handling by mitochondria is different together with the sensitivity to apoptosis triggered via this pathway. Finally, according to the above, we were able to determine which one among the clones represents the suitable stem cell. CONCLUSIONS: These experimental observations report novel physiological features in the cell biology of SCs and refer to an intrinsic heterogeneity within which their stemness may reside. BioMed Central 2013-05-03 /pmc/articles/PMC3689622/ /pubmed/23641781 http://dx.doi.org/10.1186/1471-2121-14-24 Text en Copyright © 2013 Repele et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Repele, Andrea Lupi, Ramona Eaton, Simon Urbani, Luca De Coppi, Paolo Campanella, Michelangelo Cell metabolism sets the differences between subpopulations of satellite cells (SCs) |
title | Cell metabolism sets the differences between subpopulations of satellite cells (SCs) |
title_full | Cell metabolism sets the differences between subpopulations of satellite cells (SCs) |
title_fullStr | Cell metabolism sets the differences between subpopulations of satellite cells (SCs) |
title_full_unstemmed | Cell metabolism sets the differences between subpopulations of satellite cells (SCs) |
title_short | Cell metabolism sets the differences between subpopulations of satellite cells (SCs) |
title_sort | cell metabolism sets the differences between subpopulations of satellite cells (scs) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3689622/ https://www.ncbi.nlm.nih.gov/pubmed/23641781 http://dx.doi.org/10.1186/1471-2121-14-24 |
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