Cargando…
Low Intensity Vibrations Augment Mesenchymal Stem Cell Proliferation and Differentiation Capacity during in vitro Expansion
A primary component of exercise, mechanical signals, when applied in the form of low intensity vibration (LIV), increases mesenchymal stem cell (MSC) osteogenesis and proliferation. While it is generally accepted that exercise effectively combats the deleterious effects of aging in the musculoskelet...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7286897/ https://www.ncbi.nlm.nih.gov/pubmed/32523117 http://dx.doi.org/10.1038/s41598-020-66055-0 |
_version_ | 1783544953281970176 |
---|---|
author | Bas, Guniz Loisate, Stacie Hudon, Stephanie F. Woods, Kali Hayden, Eric J. Pu, Xinzhu Beard, Richard Oxford, Julia T. Uzer, Gunes |
author_facet | Bas, Guniz Loisate, Stacie Hudon, Stephanie F. Woods, Kali Hayden, Eric J. Pu, Xinzhu Beard, Richard Oxford, Julia T. Uzer, Gunes |
author_sort | Bas, Guniz |
collection | PubMed |
description | A primary component of exercise, mechanical signals, when applied in the form of low intensity vibration (LIV), increases mesenchymal stem cell (MSC) osteogenesis and proliferation. While it is generally accepted that exercise effectively combats the deleterious effects of aging in the musculoskeletal system, how long-term exercise affects stem cell aging, which is typified by reduced proliferative and differentiative capacity, is not well explored. As a first step in understanding the effect of long-term application of mechanical signals on stem cell function, we investigated the effect of LIV during in vitro expansion of MSCs. Primary MSCs were subjected to either a control or to a twice-daily LIV regimen for up to sixty cell passages (P60) under in vitro cell expansion conditions. LIV effects were assessed at both early passage (EP) and late passage (LP). At the end of the experiment, P60 cultures exposed to LIV maintained a 28% increase of cell doubling and a 39% reduction in senescence-associated β-galactosidase activity (p < 0.01) but no changes in telomere lengths and p16(INK4a) levels were observed. Prolonged culture-associated decreases in osteogenic and adipogenic capacity were partially protected by LIV in both EP and LP groups (p < 0.05). Mass spectroscopy of late passage MSC indicated a synergistic decrease of actin and microtubule cytoskeleton-associated proteins in both control and LIV groups while LIV induced a recovery of proteins associated with oxidative reductase activity. In summary, our findings show that the application of long-term mechanical challenge (+LIV) during in vitro expansion of MSCs for sixty passages significantly alters MSC proliferation, differentiation and structure. This suggests LIV as a potential tool to investigate the role of physical activity during aging. |
format | Online Article Text |
id | pubmed-7286897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72868972020-06-15 Low Intensity Vibrations Augment Mesenchymal Stem Cell Proliferation and Differentiation Capacity during in vitro Expansion Bas, Guniz Loisate, Stacie Hudon, Stephanie F. Woods, Kali Hayden, Eric J. Pu, Xinzhu Beard, Richard Oxford, Julia T. Uzer, Gunes Sci Rep Article A primary component of exercise, mechanical signals, when applied in the form of low intensity vibration (LIV), increases mesenchymal stem cell (MSC) osteogenesis and proliferation. While it is generally accepted that exercise effectively combats the deleterious effects of aging in the musculoskeletal system, how long-term exercise affects stem cell aging, which is typified by reduced proliferative and differentiative capacity, is not well explored. As a first step in understanding the effect of long-term application of mechanical signals on stem cell function, we investigated the effect of LIV during in vitro expansion of MSCs. Primary MSCs were subjected to either a control or to a twice-daily LIV regimen for up to sixty cell passages (P60) under in vitro cell expansion conditions. LIV effects were assessed at both early passage (EP) and late passage (LP). At the end of the experiment, P60 cultures exposed to LIV maintained a 28% increase of cell doubling and a 39% reduction in senescence-associated β-galactosidase activity (p < 0.01) but no changes in telomere lengths and p16(INK4a) levels were observed. Prolonged culture-associated decreases in osteogenic and adipogenic capacity were partially protected by LIV in both EP and LP groups (p < 0.05). Mass spectroscopy of late passage MSC indicated a synergistic decrease of actin and microtubule cytoskeleton-associated proteins in both control and LIV groups while LIV induced a recovery of proteins associated with oxidative reductase activity. In summary, our findings show that the application of long-term mechanical challenge (+LIV) during in vitro expansion of MSCs for sixty passages significantly alters MSC proliferation, differentiation and structure. This suggests LIV as a potential tool to investigate the role of physical activity during aging. Nature Publishing Group UK 2020-06-10 /pmc/articles/PMC7286897/ /pubmed/32523117 http://dx.doi.org/10.1038/s41598-020-66055-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Bas, Guniz Loisate, Stacie Hudon, Stephanie F. Woods, Kali Hayden, Eric J. Pu, Xinzhu Beard, Richard Oxford, Julia T. Uzer, Gunes Low Intensity Vibrations Augment Mesenchymal Stem Cell Proliferation and Differentiation Capacity during in vitro Expansion |
title | Low Intensity Vibrations Augment Mesenchymal Stem Cell Proliferation and Differentiation Capacity during in vitro Expansion |
title_full | Low Intensity Vibrations Augment Mesenchymal Stem Cell Proliferation and Differentiation Capacity during in vitro Expansion |
title_fullStr | Low Intensity Vibrations Augment Mesenchymal Stem Cell Proliferation and Differentiation Capacity during in vitro Expansion |
title_full_unstemmed | Low Intensity Vibrations Augment Mesenchymal Stem Cell Proliferation and Differentiation Capacity during in vitro Expansion |
title_short | Low Intensity Vibrations Augment Mesenchymal Stem Cell Proliferation and Differentiation Capacity during in vitro Expansion |
title_sort | low intensity vibrations augment mesenchymal stem cell proliferation and differentiation capacity during in vitro expansion |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7286897/ https://www.ncbi.nlm.nih.gov/pubmed/32523117 http://dx.doi.org/10.1038/s41598-020-66055-0 |
work_keys_str_mv | AT basguniz lowintensityvibrationsaugmentmesenchymalstemcellproliferationanddifferentiationcapacityduringinvitroexpansion AT loisatestacie lowintensityvibrationsaugmentmesenchymalstemcellproliferationanddifferentiationcapacityduringinvitroexpansion AT hudonstephanief lowintensityvibrationsaugmentmesenchymalstemcellproliferationanddifferentiationcapacityduringinvitroexpansion AT woodskali lowintensityvibrationsaugmentmesenchymalstemcellproliferationanddifferentiationcapacityduringinvitroexpansion AT haydenericj lowintensityvibrationsaugmentmesenchymalstemcellproliferationanddifferentiationcapacityduringinvitroexpansion AT puxinzhu lowintensityvibrationsaugmentmesenchymalstemcellproliferationanddifferentiationcapacityduringinvitroexpansion AT beardrichard lowintensityvibrationsaugmentmesenchymalstemcellproliferationanddifferentiationcapacityduringinvitroexpansion AT oxfordjuliat lowintensityvibrationsaugmentmesenchymalstemcellproliferationanddifferentiationcapacityduringinvitroexpansion AT uzergunes lowintensityvibrationsaugmentmesenchymalstemcellproliferationanddifferentiationcapacityduringinvitroexpansion |