Protection of the muscle stem cell state from premature differentiation

The extraordinary capacity of regeneration exists in just certain species and tissue types. Invertebrates, the cells that regenerate tissues are called stem cells. During adulthood, damaged muscle tissue regenerates through Satellite stem cells that re-enter the cell cycle from a quiescent state, gi...

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Main Author: Berti, Federica
Other Authors: Dietrich, Susanne ; Guille, Matthew John ; Schubert, Frank
Published: University of Portsmouth 2016
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Online Access:https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.714168
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spelling ndltd-bl.uk-oai-ethos.bl.uk-7141682018-09-05T03:32:40ZProtection of the muscle stem cell state from premature differentiationBerti, FedericaDietrich, Susanne ; Guille, Matthew John ; Schubert, Frank2016The extraordinary capacity of regeneration exists in just certain species and tissue types. Invertebrates, the cells that regenerate tissues are called stem cells. During adulthood, damaged muscle tissue regenerates through Satellite stem cells that re-enter the cell cycle from a quiescent state, giving rise to new muscle tissue. During development, newly forming organisms build tissues through proliferating stem cells that renew the stem cell pool whilst generating myogenic stem cells which will eventually differentiate into muscle cells. For many years the Myogenic Regulatory Factors (Mrf) genes have been considered to be the main genes driving this proliferation in adult and fetal stages. Mrf genes have been shown to be capable of inducing non-myogenic cells to enter the myogenic lineage in vitro, but their role and capabilities in vivo have been less well characterised. Here we show, using the developing chicken model, that Mrf genes and related genes are not capable of prematurely upregulating terminal muscle differentiation before HH20. MyoD and other combinations of gene misexpression were however shown to be capable of inducing Myosin upregulation between HH20 and HH24 indicating the existence of a time-frame dependent protection of premature development. These results indicate that the Mrf genes have a reduced proficiency for inducing differentiation in vivo compared with in vitro likely due to the presence of currently unidentified additional factors. Our results demonstrate that the current understanding of the signals and cues of muscle stem cell differentiation are still insufficient to exploit the regenerative capabilities of muscle tissues towards regenerative therapies. The possible additional factors required for muscle stem cell differentiation are also discussed.616.02University of Portsmouthhttps://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.714168https://researchportal.port.ac.uk/portal/en/theses/protection-of-the-muscle-stem-cell-state-from-premature-differentiation(6886509a-35fa-43b1-8971-7cb2dcaa7da3).htmlElectronic Thesis or Dissertation
collection NDLTD
sources NDLTD
topic 616.02
spellingShingle 616.02
Berti, Federica
Protection of the muscle stem cell state from premature differentiation
description The extraordinary capacity of regeneration exists in just certain species and tissue types. Invertebrates, the cells that regenerate tissues are called stem cells. During adulthood, damaged muscle tissue regenerates through Satellite stem cells that re-enter the cell cycle from a quiescent state, giving rise to new muscle tissue. During development, newly forming organisms build tissues through proliferating stem cells that renew the stem cell pool whilst generating myogenic stem cells which will eventually differentiate into muscle cells. For many years the Myogenic Regulatory Factors (Mrf) genes have been considered to be the main genes driving this proliferation in adult and fetal stages. Mrf genes have been shown to be capable of inducing non-myogenic cells to enter the myogenic lineage in vitro, but their role and capabilities in vivo have been less well characterised. Here we show, using the developing chicken model, that Mrf genes and related genes are not capable of prematurely upregulating terminal muscle differentiation before HH20. MyoD and other combinations of gene misexpression were however shown to be capable of inducing Myosin upregulation between HH20 and HH24 indicating the existence of a time-frame dependent protection of premature development. These results indicate that the Mrf genes have a reduced proficiency for inducing differentiation in vivo compared with in vitro likely due to the presence of currently unidentified additional factors. Our results demonstrate that the current understanding of the signals and cues of muscle stem cell differentiation are still insufficient to exploit the regenerative capabilities of muscle tissues towards regenerative therapies. The possible additional factors required for muscle stem cell differentiation are also discussed.
author2 Dietrich, Susanne ; Guille, Matthew John ; Schubert, Frank
author_facet Dietrich, Susanne ; Guille, Matthew John ; Schubert, Frank
Berti, Federica
author Berti, Federica
author_sort Berti, Federica
title Protection of the muscle stem cell state from premature differentiation
title_short Protection of the muscle stem cell state from premature differentiation
title_full Protection of the muscle stem cell state from premature differentiation
title_fullStr Protection of the muscle stem cell state from premature differentiation
title_full_unstemmed Protection of the muscle stem cell state from premature differentiation
title_sort protection of the muscle stem cell state from premature differentiation
publisher University of Portsmouth
publishDate 2016
url https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.714168
work_keys_str_mv AT bertifederica protectionofthemusclestemcellstatefromprematuredifferentiation
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