Pulpbow: A Method to Study the Vasculogenic Potential of Mesenchymal Stem Cells from the Dental Pulp

Understanding how Mesenchymal Stem Cells (MSCs) form blood vessels is critical for creating mechanism-based approaches for the therapeutic use of these cells. In addition, understanding the determinants and factors involved in lineage hierarchy is fundamental to creating accurate and reliable techni...

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Autores principales: Andrea Mantesso, Zhaocheng Zhang, Kristy A. Warner, Alexandra E. Herzog, Ajai J. Pulianmackal, Jacques E. Nör
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Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:2f73ad61635447c5924ac54b3b1591722021-11-25T17:07:15ZPulpbow: A Method to Study the Vasculogenic Potential of Mesenchymal Stem Cells from the Dental Pulp10.3390/cells101128042073-4409https://doaj.org/article/2f73ad61635447c5924ac54b3b1591722021-10-01T00:00:00Zhttps://www.mdpi.com/2073-4409/10/11/2804https://doaj.org/toc/2073-4409Understanding how Mesenchymal Stem Cells (MSCs) form blood vessels is critical for creating mechanism-based approaches for the therapeutic use of these cells. In addition, understanding the determinants and factors involved in lineage hierarchy is fundamental to creating accurate and reliable techniques for the study of stem cells in tissue engineering and repair. Dental Pulp Stem Cells (DPSC) from permanent teeth and Stem cells from Human Exfoliated Deciduous teeth (SHED) are particularly interesting sources for tissue engineering as they are easily accessible and expandable. Previously, we have shown that DPSCs and SHEDs can differentiate into endothelial cells and form functional blood vessels through vasculogenesis. Here, we described how we created the “pulpbow” (pulp + rainbow), a multicolor tag experimental model that is stable, permanent, unique to each cell and passed through generations. We used the pulpbow to understand how dental pulp stem cells contributed to blood vessel formation in 3D models in in vitro and ex vivo live cell tracking, and in vivo transplantation assays. Simultaneous tracking of cells during sprout formation revealed that no single multicolor-tagged cell was more prone to vasculogenesis. During this process, there was intense cell motility with minimal proliferation in early time points. In later stages, when the availability of undifferentiated cells around the forming sprout decreased, there was local clonal proliferation mediated by proximity. These results unveiled that the vasculogenesis process mediated by dental pulp stem cells is dynamic and proximity to the sprouting area is critical for cell fate decisions.Andrea MantessoZhaocheng ZhangKristy A. WarnerAlexandra E. HerzogAjai J. PulianmackalJacques E. NörMDPI AGarticlevasculogenesisangiogenesistissue regenerationendothelial cellscell fatestemnessBiology (General)QH301-705.5ENCells, Vol 10, Iss 2804, p 2804 (2021)
institution DOAJ
collection DOAJ
language EN
topic vasculogenesis
angiogenesis
tissue regeneration
endothelial cells
cell fate
stemness
Biology (General)
QH301-705.5
spellingShingle vasculogenesis
angiogenesis
tissue regeneration
endothelial cells
cell fate
stemness
Biology (General)
QH301-705.5
Andrea Mantesso
Zhaocheng Zhang
Kristy A. Warner
Alexandra E. Herzog
Ajai J. Pulianmackal
Jacques E. Nör
Pulpbow: A Method to Study the Vasculogenic Potential of Mesenchymal Stem Cells from the Dental Pulp
description Understanding how Mesenchymal Stem Cells (MSCs) form blood vessels is critical for creating mechanism-based approaches for the therapeutic use of these cells. In addition, understanding the determinants and factors involved in lineage hierarchy is fundamental to creating accurate and reliable techniques for the study of stem cells in tissue engineering and repair. Dental Pulp Stem Cells (DPSC) from permanent teeth and Stem cells from Human Exfoliated Deciduous teeth (SHED) are particularly interesting sources for tissue engineering as they are easily accessible and expandable. Previously, we have shown that DPSCs and SHEDs can differentiate into endothelial cells and form functional blood vessels through vasculogenesis. Here, we described how we created the “pulpbow” (pulp + rainbow), a multicolor tag experimental model that is stable, permanent, unique to each cell and passed through generations. We used the pulpbow to understand how dental pulp stem cells contributed to blood vessel formation in 3D models in in vitro and ex vivo live cell tracking, and in vivo transplantation assays. Simultaneous tracking of cells during sprout formation revealed that no single multicolor-tagged cell was more prone to vasculogenesis. During this process, there was intense cell motility with minimal proliferation in early time points. In later stages, when the availability of undifferentiated cells around the forming sprout decreased, there was local clonal proliferation mediated by proximity. These results unveiled that the vasculogenesis process mediated by dental pulp stem cells is dynamic and proximity to the sprouting area is critical for cell fate decisions.
format article
author Andrea Mantesso
Zhaocheng Zhang
Kristy A. Warner
Alexandra E. Herzog
Ajai J. Pulianmackal
Jacques E. Nör
author_facet Andrea Mantesso
Zhaocheng Zhang
Kristy A. Warner
Alexandra E. Herzog
Ajai J. Pulianmackal
Jacques E. Nör
author_sort Andrea Mantesso
title Pulpbow: A Method to Study the Vasculogenic Potential of Mesenchymal Stem Cells from the Dental Pulp
title_short Pulpbow: A Method to Study the Vasculogenic Potential of Mesenchymal Stem Cells from the Dental Pulp
title_full Pulpbow: A Method to Study the Vasculogenic Potential of Mesenchymal Stem Cells from the Dental Pulp
title_fullStr Pulpbow: A Method to Study the Vasculogenic Potential of Mesenchymal Stem Cells from the Dental Pulp
title_full_unstemmed Pulpbow: A Method to Study the Vasculogenic Potential of Mesenchymal Stem Cells from the Dental Pulp
title_sort pulpbow: a method to study the vasculogenic potential of mesenchymal stem cells from the dental pulp
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/2f73ad61635447c5924ac54b3b159172
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