Prolonged mechanical stretch initiates intracellular calcium oscillations in human mesenchymal stem cells.

Mesenchymal stem cells (MSCs) are a promising candidate for cell-based therapy in regenerative medicine. These stem cells can interact with their mechanical microenvironment to control their functions. External mechanical cues can be perceived and transmitted into intracellular calcium dynamics to r...

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Main Authors: Tae-Jin Kim, Jie Sun, Shaoying Lu, Ying-Xin Qi, Yingxiao Wang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4203723?pdf=render
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spelling doaj-e8d12e149c944af69fc83874a3c4adbc2020-11-25T01:30:59ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-01910e10937810.1371/journal.pone.0109378Prolonged mechanical stretch initiates intracellular calcium oscillations in human mesenchymal stem cells.Tae-Jin KimJie SunShaoying LuYing-Xin QiYingxiao WangMesenchymal stem cells (MSCs) are a promising candidate for cell-based therapy in regenerative medicine. These stem cells can interact with their mechanical microenvironment to control their functions. External mechanical cues can be perceived and transmitted into intracellular calcium dynamics to regulate various cellular processes. Recent studies indicate that human MSCs (hMSCs) exhibit a heterogeneous nature with a subset of hMSCs lacking spontaneous calcium oscillations. In this study, we studied whether and how external mechanical tension can be applied to trigger and restore the intracellular calcium oscillation in these hMSCs lacking spontaneous activities. Utilizing the fluorescence resonance energy transfer (FRET) based calcium biosensor, we found that this subpopulation of hMSCs can respond to a prolonged mechanical stretch (PMS). Further results revealed that the triggering of calcium oscillations in these cells is dependent on the calcium influx across the plasma membrane, as well as on both cytoskeletal supports, myosin light chain kinase (MLCK)-driven actomyosin contractility, and phospholipase C (PLC) activity. Thus, our report confirmed that mechanical tension can govern the intracellular calcium oscillation in hMSCs, possibly via the control of the calcium permeability of channels at the plasma membrane. Our results also provide novel mechanistic insights into how hMSCs sense mechanical environment to regulate cellular functions.http://europepmc.org/articles/PMC4203723?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Tae-Jin Kim
Jie Sun
Shaoying Lu
Ying-Xin Qi
Yingxiao Wang
spellingShingle Tae-Jin Kim
Jie Sun
Shaoying Lu
Ying-Xin Qi
Yingxiao Wang
Prolonged mechanical stretch initiates intracellular calcium oscillations in human mesenchymal stem cells.
PLoS ONE
author_facet Tae-Jin Kim
Jie Sun
Shaoying Lu
Ying-Xin Qi
Yingxiao Wang
author_sort Tae-Jin Kim
title Prolonged mechanical stretch initiates intracellular calcium oscillations in human mesenchymal stem cells.
title_short Prolonged mechanical stretch initiates intracellular calcium oscillations in human mesenchymal stem cells.
title_full Prolonged mechanical stretch initiates intracellular calcium oscillations in human mesenchymal stem cells.
title_fullStr Prolonged mechanical stretch initiates intracellular calcium oscillations in human mesenchymal stem cells.
title_full_unstemmed Prolonged mechanical stretch initiates intracellular calcium oscillations in human mesenchymal stem cells.
title_sort prolonged mechanical stretch initiates intracellular calcium oscillations in human mesenchymal stem cells.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Mesenchymal stem cells (MSCs) are a promising candidate for cell-based therapy in regenerative medicine. These stem cells can interact with their mechanical microenvironment to control their functions. External mechanical cues can be perceived and transmitted into intracellular calcium dynamics to regulate various cellular processes. Recent studies indicate that human MSCs (hMSCs) exhibit a heterogeneous nature with a subset of hMSCs lacking spontaneous calcium oscillations. In this study, we studied whether and how external mechanical tension can be applied to trigger and restore the intracellular calcium oscillation in these hMSCs lacking spontaneous activities. Utilizing the fluorescence resonance energy transfer (FRET) based calcium biosensor, we found that this subpopulation of hMSCs can respond to a prolonged mechanical stretch (PMS). Further results revealed that the triggering of calcium oscillations in these cells is dependent on the calcium influx across the plasma membrane, as well as on both cytoskeletal supports, myosin light chain kinase (MLCK)-driven actomyosin contractility, and phospholipase C (PLC) activity. Thus, our report confirmed that mechanical tension can govern the intracellular calcium oscillation in hMSCs, possibly via the control of the calcium permeability of channels at the plasma membrane. Our results also provide novel mechanistic insights into how hMSCs sense mechanical environment to regulate cellular functions.
url http://europepmc.org/articles/PMC4203723?pdf=render
work_keys_str_mv AT taejinkim prolongedmechanicalstretchinitiatesintracellularcalciumoscillationsinhumanmesenchymalstemcells
AT jiesun prolongedmechanicalstretchinitiatesintracellularcalciumoscillationsinhumanmesenchymalstemcells
AT shaoyinglu prolongedmechanicalstretchinitiatesintracellularcalciumoscillationsinhumanmesenchymalstemcells
AT yingxinqi prolongedmechanicalstretchinitiatesintracellularcalciumoscillationsinhumanmesenchymalstemcells
AT yingxiaowang prolongedmechanicalstretchinitiatesintracellularcalciumoscillationsinhumanmesenchymalstemcells
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