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Between Fate Choice and Self-Renewal—Heterogeneity of Adult Neural Crest-Derived Stem Cells

Stem cells of the neural crest (NC) vitally participate to embryonic development, but also remain in distinct niches as quiescent neural crest-derived stem cell (NCSC) pools into adulthood. Although NCSC-populations share a high capacity for self-renewal and differentiation resulting in promising pr...

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Autores principales: Höving, Anna L., Windmöller, Beatrice A., Knabbe, Cornelius, Kaltschmidt, Barbara, Kaltschmidt, Christian, Greiner, Johannes F. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8060484/
https://www.ncbi.nlm.nih.gov/pubmed/33898464
http://dx.doi.org/10.3389/fcell.2021.662754
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author Höving, Anna L.
Windmöller, Beatrice A.
Knabbe, Cornelius
Kaltschmidt, Barbara
Kaltschmidt, Christian
Greiner, Johannes F. W.
author_facet Höving, Anna L.
Windmöller, Beatrice A.
Knabbe, Cornelius
Kaltschmidt, Barbara
Kaltschmidt, Christian
Greiner, Johannes F. W.
author_sort Höving, Anna L.
collection PubMed
description Stem cells of the neural crest (NC) vitally participate to embryonic development, but also remain in distinct niches as quiescent neural crest-derived stem cell (NCSC) pools into adulthood. Although NCSC-populations share a high capacity for self-renewal and differentiation resulting in promising preclinical applications within the last two decades, inter- and intrapopulational differences exist in terms of their expression signatures and regenerative capability. Differentiation and self-renewal of stem cells in developmental and regenerative contexts are partially regulated by the niche or culture condition and further influenced by single cell decision processes, making cell-to-cell variation and heterogeneity critical for understanding adult stem cell populations. The present review summarizes current knowledge of the cellular heterogeneity within NCSC-populations located in distinct craniofacial and trunk niches including the nasal cavity, olfactory bulb, oral tissues or skin. We shed light on the impact of intrapopulational heterogeneity on fate specifications and plasticity of NCSCs in their niches in vivo as well as during in vitro culture. We further discuss underlying molecular regulators determining fate specifications of NCSCs, suggesting a regulatory network including NF-κB and NC-related transcription factors like SLUG and SOX9 accompanied by Wnt- and MAPK-signaling to orchestrate NCSC stemness and differentiation. In summary, adult NCSCs show a broad heterogeneity on the level of the donor and the donors’ sex, the cell population and the single stem cell directly impacting their differentiation capability and fate choices in vivo and in vitro. The findings discussed here emphasize heterogeneity of NCSCs as a crucial parameter for understanding their role in tissue homeostasis and regeneration and for improving their applicability in regenerative medicine.
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spelling pubmed-80604842021-04-23 Between Fate Choice and Self-Renewal—Heterogeneity of Adult Neural Crest-Derived Stem Cells Höving, Anna L. Windmöller, Beatrice A. Knabbe, Cornelius Kaltschmidt, Barbara Kaltschmidt, Christian Greiner, Johannes F. W. Front Cell Dev Biol Cell and Developmental Biology Stem cells of the neural crest (NC) vitally participate to embryonic development, but also remain in distinct niches as quiescent neural crest-derived stem cell (NCSC) pools into adulthood. Although NCSC-populations share a high capacity for self-renewal and differentiation resulting in promising preclinical applications within the last two decades, inter- and intrapopulational differences exist in terms of their expression signatures and regenerative capability. Differentiation and self-renewal of stem cells in developmental and regenerative contexts are partially regulated by the niche or culture condition and further influenced by single cell decision processes, making cell-to-cell variation and heterogeneity critical for understanding adult stem cell populations. The present review summarizes current knowledge of the cellular heterogeneity within NCSC-populations located in distinct craniofacial and trunk niches including the nasal cavity, olfactory bulb, oral tissues or skin. We shed light on the impact of intrapopulational heterogeneity on fate specifications and plasticity of NCSCs in their niches in vivo as well as during in vitro culture. We further discuss underlying molecular regulators determining fate specifications of NCSCs, suggesting a regulatory network including NF-κB and NC-related transcription factors like SLUG and SOX9 accompanied by Wnt- and MAPK-signaling to orchestrate NCSC stemness and differentiation. In summary, adult NCSCs show a broad heterogeneity on the level of the donor and the donors’ sex, the cell population and the single stem cell directly impacting their differentiation capability and fate choices in vivo and in vitro. The findings discussed here emphasize heterogeneity of NCSCs as a crucial parameter for understanding their role in tissue homeostasis and regeneration and for improving their applicability in regenerative medicine. Frontiers Media S.A. 2021-04-08 /pmc/articles/PMC8060484/ /pubmed/33898464 http://dx.doi.org/10.3389/fcell.2021.662754 Text en Copyright © 2021 Höving, Windmöller, Knabbe, Kaltschmidt, Kaltschmidt and Greiner. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Höving, Anna L.
Windmöller, Beatrice A.
Knabbe, Cornelius
Kaltschmidt, Barbara
Kaltschmidt, Christian
Greiner, Johannes F. W.
Between Fate Choice and Self-Renewal—Heterogeneity of Adult Neural Crest-Derived Stem Cells
title Between Fate Choice and Self-Renewal—Heterogeneity of Adult Neural Crest-Derived Stem Cells
title_full Between Fate Choice and Self-Renewal—Heterogeneity of Adult Neural Crest-Derived Stem Cells
title_fullStr Between Fate Choice and Self-Renewal—Heterogeneity of Adult Neural Crest-Derived Stem Cells
title_full_unstemmed Between Fate Choice and Self-Renewal—Heterogeneity of Adult Neural Crest-Derived Stem Cells
title_short Between Fate Choice and Self-Renewal—Heterogeneity of Adult Neural Crest-Derived Stem Cells
title_sort between fate choice and self-renewal—heterogeneity of adult neural crest-derived stem cells
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8060484/
https://www.ncbi.nlm.nih.gov/pubmed/33898464
http://dx.doi.org/10.3389/fcell.2021.662754
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