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Development and Characterization of Alkaline Phosphatase-Positive Human Umbilical Cord Perivascular Cells
Human umbilical cord perivascular cells (HUCPVCs), harvested from human umbilical cord perivascular tissue, show potential for future use as an alternative to mesenchymal stromal cells. Here, we present the results for the characterization of the properties alkaline phosphatase-positive HUCPVCs (ALP...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8616437/ https://www.ncbi.nlm.nih.gov/pubmed/34831233 http://dx.doi.org/10.3390/cells10113011 |
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author | Nonoyama, Shun Karakida, Takeo Chiba-Ohkuma, Risako Yamamoto, Ryuji Ujiie, Yuko Nagano, Takatoshi Yamakoshi, Yasuo Gomi, Kazuhiro |
author_facet | Nonoyama, Shun Karakida, Takeo Chiba-Ohkuma, Risako Yamamoto, Ryuji Ujiie, Yuko Nagano, Takatoshi Yamakoshi, Yasuo Gomi, Kazuhiro |
author_sort | Nonoyama, Shun |
collection | PubMed |
description | Human umbilical cord perivascular cells (HUCPVCs), harvested from human umbilical cord perivascular tissue, show potential for future use as an alternative to mesenchymal stromal cells. Here, we present the results for the characterization of the properties alkaline phosphatase-positive HUCPVCs (ALP(+)-HUCPVCs). These ALP(+)-HUCPVCs were created from HUCPVCs in this study by culturing in the presence of activated vitamin D3, an inhibitor of bone morphogenetic protein signaling and transforming growth factor-beta1 (TGF-β1). The morphological characteristics, cell proliferation, gene expression, and mineralization-inducing ability of ALP(+)-HUCPVCs were investigated at the morphological, biological, and genetic levels. ALP(+)-HUCPVCs possess high ALP gene expression and activity in cells and a slow rate of cell growth. The morphology of ALP(+)-HUCPVCs is fibroblast-like, with an increase in actin filaments containing alpha-smooth muscle actin. In addition to ALP expression, the gene expression levels of type I collagen, osteopontin, elastin, fibrillin-1, and cluster of differentiation 90 are increased in ALP(+)-HUCPVCs. ALP(+)-HUCPVCs do not have the ability to induce mineralization nodules, which may be due to the restriction of phosphate uptake into matrix vesicles. Moreover, ALP(+)-HUCPVCs may produce anti-mineralization substances. We conclude that ALP(+)-HUCPVCs induced from HUCPVCs by a TGF-β1 stimulation possess myofibroblast-like properties that have little mineralization-inducing ability. |
format | Online Article Text |
id | pubmed-8616437 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86164372021-11-26 Development and Characterization of Alkaline Phosphatase-Positive Human Umbilical Cord Perivascular Cells Nonoyama, Shun Karakida, Takeo Chiba-Ohkuma, Risako Yamamoto, Ryuji Ujiie, Yuko Nagano, Takatoshi Yamakoshi, Yasuo Gomi, Kazuhiro Cells Article Human umbilical cord perivascular cells (HUCPVCs), harvested from human umbilical cord perivascular tissue, show potential for future use as an alternative to mesenchymal stromal cells. Here, we present the results for the characterization of the properties alkaline phosphatase-positive HUCPVCs (ALP(+)-HUCPVCs). These ALP(+)-HUCPVCs were created from HUCPVCs in this study by culturing in the presence of activated vitamin D3, an inhibitor of bone morphogenetic protein signaling and transforming growth factor-beta1 (TGF-β1). The morphological characteristics, cell proliferation, gene expression, and mineralization-inducing ability of ALP(+)-HUCPVCs were investigated at the morphological, biological, and genetic levels. ALP(+)-HUCPVCs possess high ALP gene expression and activity in cells and a slow rate of cell growth. The morphology of ALP(+)-HUCPVCs is fibroblast-like, with an increase in actin filaments containing alpha-smooth muscle actin. In addition to ALP expression, the gene expression levels of type I collagen, osteopontin, elastin, fibrillin-1, and cluster of differentiation 90 are increased in ALP(+)-HUCPVCs. ALP(+)-HUCPVCs do not have the ability to induce mineralization nodules, which may be due to the restriction of phosphate uptake into matrix vesicles. Moreover, ALP(+)-HUCPVCs may produce anti-mineralization substances. We conclude that ALP(+)-HUCPVCs induced from HUCPVCs by a TGF-β1 stimulation possess myofibroblast-like properties that have little mineralization-inducing ability. MDPI 2021-11-04 /pmc/articles/PMC8616437/ /pubmed/34831233 http://dx.doi.org/10.3390/cells10113011 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Nonoyama, Shun Karakida, Takeo Chiba-Ohkuma, Risako Yamamoto, Ryuji Ujiie, Yuko Nagano, Takatoshi Yamakoshi, Yasuo Gomi, Kazuhiro Development and Characterization of Alkaline Phosphatase-Positive Human Umbilical Cord Perivascular Cells |
title | Development and Characterization of Alkaline Phosphatase-Positive Human Umbilical Cord Perivascular Cells |
title_full | Development and Characterization of Alkaline Phosphatase-Positive Human Umbilical Cord Perivascular Cells |
title_fullStr | Development and Characterization of Alkaline Phosphatase-Positive Human Umbilical Cord Perivascular Cells |
title_full_unstemmed | Development and Characterization of Alkaline Phosphatase-Positive Human Umbilical Cord Perivascular Cells |
title_short | Development and Characterization of Alkaline Phosphatase-Positive Human Umbilical Cord Perivascular Cells |
title_sort | development and characterization of alkaline phosphatase-positive human umbilical cord perivascular cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8616437/ https://www.ncbi.nlm.nih.gov/pubmed/34831233 http://dx.doi.org/10.3390/cells10113011 |
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