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Muscle satellite cell proliferation and association: new insights from myofiber time-lapse imaging
BACKGROUND: As the resident stem cells of skeletal muscle, satellite cells are activated by extracellular cues associated with local damage. Once activated, satellite cells will re-enter the cell cycle to proliferate and supply a population of myoblasts, which will repair or replace damaged myofiber...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3157006/ https://www.ncbi.nlm.nih.gov/pubmed/21798086 http://dx.doi.org/10.1186/2044-5040-1-7 |
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author | Siegel, Ashley L Kuhlmann, Paige K Cornelison, DDW |
author_facet | Siegel, Ashley L Kuhlmann, Paige K Cornelison, DDW |
author_sort | Siegel, Ashley L |
collection | PubMed |
description | BACKGROUND: As the resident stem cells of skeletal muscle, satellite cells are activated by extracellular cues associated with local damage. Once activated, satellite cells will re-enter the cell cycle to proliferate and supply a population of myoblasts, which will repair or replace damaged myofibers by differentiating and fusing either with an existing myofiber or with each other. There is also evidence that the orientation of cell division with respect to the myofiber may indicate or convey asymmetry in the two daughter cells. Our recent studies with time-lapse imaging of myofiber-associated satellite cells in vitro have yielded new data on the timing and orientation of satellite cell divisions, and revealed persistent differences in the behavior of daughter cells from planar versus vertical divisions. RESULTS: We analyzed 244 individual fiber-associated satellite cells in time-lapse video from 24 to 48 hours after myofiber harvest. We found that initial cell division in fiber culture is not synchronous, although presumably all cells were activated by the initial trauma of harvest; that cell cycling time is significantly shorter than previously thought (as short as 4.8 hours, averaging 10 hours between the first and second divisions and eight hours between the second and third); and that timing of subsequent divisions is not strongly correlated with timing of the initial division. Approximately 65% of first and 80% of second cell divisions occur parallel to the axis of the myofiber, whereas the remainder occur outside the plane of the fiber surface (vertical division). We previously demonstrated that daughter cells frequently remain associated with each other after division or reassociate after a brief separation, and that unrelated cells may also associate for significant periods of time. We show in this paper that daughter cells resulting from a vertical division remain associated with one another several times longer than do daughters from a horizontal division. However, the total average time of association between sister cells is not significantly different from the total average time of association between unrelated cells. CONCLUSIONS: These longitudinal characterizations of satellite cell behavior shortly after activation provide new insights into cell proliferation and association as a function of relatedness, and indicate significant and consistent heterogeneity within the population based on these metrics. |
format | Online Article Text |
id | pubmed-3157006 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31570062011-08-17 Muscle satellite cell proliferation and association: new insights from myofiber time-lapse imaging Siegel, Ashley L Kuhlmann, Paige K Cornelison, DDW Skelet Muscle Research BACKGROUND: As the resident stem cells of skeletal muscle, satellite cells are activated by extracellular cues associated with local damage. Once activated, satellite cells will re-enter the cell cycle to proliferate and supply a population of myoblasts, which will repair or replace damaged myofibers by differentiating and fusing either with an existing myofiber or with each other. There is also evidence that the orientation of cell division with respect to the myofiber may indicate or convey asymmetry in the two daughter cells. Our recent studies with time-lapse imaging of myofiber-associated satellite cells in vitro have yielded new data on the timing and orientation of satellite cell divisions, and revealed persistent differences in the behavior of daughter cells from planar versus vertical divisions. RESULTS: We analyzed 244 individual fiber-associated satellite cells in time-lapse video from 24 to 48 hours after myofiber harvest. We found that initial cell division in fiber culture is not synchronous, although presumably all cells were activated by the initial trauma of harvest; that cell cycling time is significantly shorter than previously thought (as short as 4.8 hours, averaging 10 hours between the first and second divisions and eight hours between the second and third); and that timing of subsequent divisions is not strongly correlated with timing of the initial division. Approximately 65% of first and 80% of second cell divisions occur parallel to the axis of the myofiber, whereas the remainder occur outside the plane of the fiber surface (vertical division). We previously demonstrated that daughter cells frequently remain associated with each other after division or reassociate after a brief separation, and that unrelated cells may also associate for significant periods of time. We show in this paper that daughter cells resulting from a vertical division remain associated with one another several times longer than do daughters from a horizontal division. However, the total average time of association between sister cells is not significantly different from the total average time of association between unrelated cells. CONCLUSIONS: These longitudinal characterizations of satellite cell behavior shortly after activation provide new insights into cell proliferation and association as a function of relatedness, and indicate significant and consistent heterogeneity within the population based on these metrics. BioMed Central 2011-02-02 /pmc/articles/PMC3157006/ /pubmed/21798086 http://dx.doi.org/10.1186/2044-5040-1-7 Text en Copyright ©2011 Siegel 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 Siegel, Ashley L Kuhlmann, Paige K Cornelison, DDW Muscle satellite cell proliferation and association: new insights from myofiber time-lapse imaging |
title | Muscle satellite cell proliferation and association: new insights from myofiber time-lapse imaging |
title_full | Muscle satellite cell proliferation and association: new insights from myofiber time-lapse imaging |
title_fullStr | Muscle satellite cell proliferation and association: new insights from myofiber time-lapse imaging |
title_full_unstemmed | Muscle satellite cell proliferation and association: new insights from myofiber time-lapse imaging |
title_short | Muscle satellite cell proliferation and association: new insights from myofiber time-lapse imaging |
title_sort | muscle satellite cell proliferation and association: new insights from myofiber time-lapse imaging |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3157006/ https://www.ncbi.nlm.nih.gov/pubmed/21798086 http://dx.doi.org/10.1186/2044-5040-1-7 |
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