Cargando…

Milieu for Endothelial Differentiation of Human Adipose-Derived Stem Cells

Human adipose-derived stem cells (hASCs) have been shown to differentiate down many lineages including endothelial lineage. We hypothesized that hASCs would more efficiently differentiate toward the endothelial lineage when formed as three-dimensional (3D) spheroids and with the addition of vascular...

Descripción completa

Detalles Bibliográficos
Autores principales: Clark, Kendra, Janorkar, Amol V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316606/
https://www.ncbi.nlm.nih.gov/pubmed/30282912
http://dx.doi.org/10.3390/bioengineering5040082
_version_ 1783384569441943552
author Clark, Kendra
Janorkar, Amol V.
author_facet Clark, Kendra
Janorkar, Amol V.
author_sort Clark, Kendra
collection PubMed
description Human adipose-derived stem cells (hASCs) have been shown to differentiate down many lineages including endothelial lineage. We hypothesized that hASCs would more efficiently differentiate toward the endothelial lineage when formed as three-dimensional (3D) spheroids and with the addition of vascular endothelial growth factor (VEGF). Three conditions were tested: uncoated tissue culture polystyrene (TCPS) surfaces that induced a 2D monolayer formation; elastin-like polypeptide (ELP)-collagen composite hydrogel scaffolds that induced encapsulated 3D spheroid culture; and ELP-polyethyleneimine-coated TCPS surfaces that induced 3D spheroid formation in scaffold-free condition. Cells were exposed to endothelial differentiation medium containing no additional VEGF or 20 and 50 ng/mL of VEGF for 7 days and assayed for viability and endothelial differentiation markers. While endothelial differentiation media supported endothelial differentiation of hASCs, our 3D spheroid cultures augmented this differentiation and produced more von Willebrand factor than 2D cultures. Likewise, 3D cultures were able to uptake LDL, whereas the 2D cultures were not. Higher concentrations of VEGF further enhanced differentiation. Establishing angiogenesis is a key factor in regenerative medicine. Future studies aim to elucidate how to produce physiological changes such as neoangiogenesis and sprouting of vessels which may enhance the survival of regenerated tissues.
format Online
Article
Text
id pubmed-6316606
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-63166062019-01-10 Milieu for Endothelial Differentiation of Human Adipose-Derived Stem Cells Clark, Kendra Janorkar, Amol V. Bioengineering (Basel) Article Human adipose-derived stem cells (hASCs) have been shown to differentiate down many lineages including endothelial lineage. We hypothesized that hASCs would more efficiently differentiate toward the endothelial lineage when formed as three-dimensional (3D) spheroids and with the addition of vascular endothelial growth factor (VEGF). Three conditions were tested: uncoated tissue culture polystyrene (TCPS) surfaces that induced a 2D monolayer formation; elastin-like polypeptide (ELP)-collagen composite hydrogel scaffolds that induced encapsulated 3D spheroid culture; and ELP-polyethyleneimine-coated TCPS surfaces that induced 3D spheroid formation in scaffold-free condition. Cells were exposed to endothelial differentiation medium containing no additional VEGF or 20 and 50 ng/mL of VEGF for 7 days and assayed for viability and endothelial differentiation markers. While endothelial differentiation media supported endothelial differentiation of hASCs, our 3D spheroid cultures augmented this differentiation and produced more von Willebrand factor than 2D cultures. Likewise, 3D cultures were able to uptake LDL, whereas the 2D cultures were not. Higher concentrations of VEGF further enhanced differentiation. Establishing angiogenesis is a key factor in regenerative medicine. Future studies aim to elucidate how to produce physiological changes such as neoangiogenesis and sprouting of vessels which may enhance the survival of regenerated tissues. MDPI 2018-10-03 /pmc/articles/PMC6316606/ /pubmed/30282912 http://dx.doi.org/10.3390/bioengineering5040082 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Clark, Kendra
Janorkar, Amol V.
Milieu for Endothelial Differentiation of Human Adipose-Derived Stem Cells
title Milieu for Endothelial Differentiation of Human Adipose-Derived Stem Cells
title_full Milieu for Endothelial Differentiation of Human Adipose-Derived Stem Cells
title_fullStr Milieu for Endothelial Differentiation of Human Adipose-Derived Stem Cells
title_full_unstemmed Milieu for Endothelial Differentiation of Human Adipose-Derived Stem Cells
title_short Milieu for Endothelial Differentiation of Human Adipose-Derived Stem Cells
title_sort milieu for endothelial differentiation of human adipose-derived stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316606/
https://www.ncbi.nlm.nih.gov/pubmed/30282912
http://dx.doi.org/10.3390/bioengineering5040082
work_keys_str_mv AT clarkkendra milieuforendothelialdifferentiationofhumanadiposederivedstemcells
AT janorkaramolv milieuforendothelialdifferentiationofhumanadiposederivedstemcells