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Endothelial Cells Promote Osteogenesis by Establishing a Functional and Metabolic Coupling With Human Mesenchymal Stem Cells
Bone formation involves a complex crosstalk between endothelial cells (EC) and osteodifferentiating stem cells. This functional interplay is greatly mediated by the paracrine and autocrine action of soluble factors released at the vasculature-bone interface. This study elucidates the molecular and f...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8787057/ https://www.ncbi.nlm.nih.gov/pubmed/35087424 http://dx.doi.org/10.3389/fphys.2021.813547 |
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author | Petrillo, Sara Genova, Tullio Chinigò, Giorgia Roato, Ilaria Scarpellino, Giorgia Kopecka, Joanna Altruda, Fiorella Tolosano, Emanuela Riganti, Chiara Mussano, Federico Munaron, Luca |
author_facet | Petrillo, Sara Genova, Tullio Chinigò, Giorgia Roato, Ilaria Scarpellino, Giorgia Kopecka, Joanna Altruda, Fiorella Tolosano, Emanuela Riganti, Chiara Mussano, Federico Munaron, Luca |
author_sort | Petrillo, Sara |
collection | PubMed |
description | Bone formation involves a complex crosstalk between endothelial cells (EC) and osteodifferentiating stem cells. This functional interplay is greatly mediated by the paracrine and autocrine action of soluble factors released at the vasculature-bone interface. This study elucidates the molecular and functional responses triggered by this intimate interaction. In this study, we showed that human dermal microvascular endothelial cells (HMEC) induced the expression of pro-angiogenic factors in stem cells from human exfoliated deciduous teeth (SHED) and sustain their osteo-differentiation at the same time. In contrast, osteodifferentiating SHED increased EC recruitment and promoted the formation of complex vascular networks. Moreover, HMEC enhanced anaerobic glycolysis in proliferating SHED without compromising their ability to undergo the oxidative metabolic shift required for adequate osteo-differentiation. Taken together, these findings provide novel insights into the molecular mechanism underlying the synergistic cooperation between EC and stem cells during bone tissue renewal. |
format | Online Article Text |
id | pubmed-8787057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87870572022-01-26 Endothelial Cells Promote Osteogenesis by Establishing a Functional and Metabolic Coupling With Human Mesenchymal Stem Cells Petrillo, Sara Genova, Tullio Chinigò, Giorgia Roato, Ilaria Scarpellino, Giorgia Kopecka, Joanna Altruda, Fiorella Tolosano, Emanuela Riganti, Chiara Mussano, Federico Munaron, Luca Front Physiol Physiology Bone formation involves a complex crosstalk between endothelial cells (EC) and osteodifferentiating stem cells. This functional interplay is greatly mediated by the paracrine and autocrine action of soluble factors released at the vasculature-bone interface. This study elucidates the molecular and functional responses triggered by this intimate interaction. In this study, we showed that human dermal microvascular endothelial cells (HMEC) induced the expression of pro-angiogenic factors in stem cells from human exfoliated deciduous teeth (SHED) and sustain their osteo-differentiation at the same time. In contrast, osteodifferentiating SHED increased EC recruitment and promoted the formation of complex vascular networks. Moreover, HMEC enhanced anaerobic glycolysis in proliferating SHED without compromising their ability to undergo the oxidative metabolic shift required for adequate osteo-differentiation. Taken together, these findings provide novel insights into the molecular mechanism underlying the synergistic cooperation between EC and stem cells during bone tissue renewal. Frontiers Media S.A. 2022-01-11 /pmc/articles/PMC8787057/ /pubmed/35087424 http://dx.doi.org/10.3389/fphys.2021.813547 Text en Copyright © 2022 Petrillo, Genova, Chinigò, Roato, Scarpellino, Kopecka, Altruda, Tolosano, Riganti, Mussano and Munaron. 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 | Physiology Petrillo, Sara Genova, Tullio Chinigò, Giorgia Roato, Ilaria Scarpellino, Giorgia Kopecka, Joanna Altruda, Fiorella Tolosano, Emanuela Riganti, Chiara Mussano, Federico Munaron, Luca Endothelial Cells Promote Osteogenesis by Establishing a Functional and Metabolic Coupling With Human Mesenchymal Stem Cells |
title | Endothelial Cells Promote Osteogenesis by Establishing a Functional and Metabolic Coupling With Human Mesenchymal Stem Cells |
title_full | Endothelial Cells Promote Osteogenesis by Establishing a Functional and Metabolic Coupling With Human Mesenchymal Stem Cells |
title_fullStr | Endothelial Cells Promote Osteogenesis by Establishing a Functional and Metabolic Coupling With Human Mesenchymal Stem Cells |
title_full_unstemmed | Endothelial Cells Promote Osteogenesis by Establishing a Functional and Metabolic Coupling With Human Mesenchymal Stem Cells |
title_short | Endothelial Cells Promote Osteogenesis by Establishing a Functional and Metabolic Coupling With Human Mesenchymal Stem Cells |
title_sort | endothelial cells promote osteogenesis by establishing a functional and metabolic coupling with human mesenchymal stem cells |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8787057/ https://www.ncbi.nlm.nih.gov/pubmed/35087424 http://dx.doi.org/10.3389/fphys.2021.813547 |
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