Cargando…

Human Placenta-Derived ECM Supports Tri-Lineage Differentiation of Human Induced Pluripotent Stem Cells

Human pluripotent stem cells (hPSCs) hold great promise for future applications in drug discovery and cell therapies. hPSC culture protocols require specific substrates and medium supplements to support cell expansion and lineage specific differentiation. The animal origin of these substrates is a s...

Descripción completa

Detalles Bibliográficos
Autores principales: Murchison, Angela C., Odanga, Justin J., Treadwell, Michelle L., Breathwaite, Erick K., Weaver, Jessica R., Lee, Jung Bok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Stem Cell Research 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691852/
https://www.ncbi.nlm.nih.gov/pubmed/32840229
http://dx.doi.org/10.15283/ijsc20074
_version_ 1783614382145536000
author Murchison, Angela C.
Odanga, Justin J.
Treadwell, Michelle L.
Breathwaite, Erick K.
Weaver, Jessica R.
Lee, Jung Bok
author_facet Murchison, Angela C.
Odanga, Justin J.
Treadwell, Michelle L.
Breathwaite, Erick K.
Weaver, Jessica R.
Lee, Jung Bok
author_sort Murchison, Angela C.
collection PubMed
description Human pluripotent stem cells (hPSCs) hold great promise for future applications in drug discovery and cell therapies. hPSC culture protocols require specific substrates and medium supplements to support cell expansion and lineage specific differentiation. The animal origin of these substrates is a severe limitation when considering the translation of hPSC derivatives to the clinic and in vitro disease modeling. The present study evaluates the use of a human placenta-derived extracellular matrix (ECM) hydrogel, HuGentra(Ⓡ), to support tri-lineage differentiation of human induced pluripotent stem cells (hiPSCs). Lineage-specific embryoid bodies (EBs) were plated onto three separate matrices, and differentiation efficiency was evaluated based on morphology, protein, and gene expression. HuGentra was found to support the differentiation of hiPSCs to all three germ layers: ectodermal, mesodermal, and endodermal lineages. hiPSCs differentiated into neurons, cardiomyocytes, and hepatocytes on HuGentra had similar morphology, protein, and gene expression compared to differentiation on Matrigel or other cell preferred matrices. HuGentra can be considered as a suitable human substrate for hiPSC differentiation.
format Online
Article
Text
id pubmed-7691852
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Korean Society for Stem Cell Research
record_format MEDLINE/PubMed
spelling pubmed-76918522020-12-07 Human Placenta-Derived ECM Supports Tri-Lineage Differentiation of Human Induced Pluripotent Stem Cells Murchison, Angela C. Odanga, Justin J. Treadwell, Michelle L. Breathwaite, Erick K. Weaver, Jessica R. Lee, Jung Bok Int J Stem Cells Brief Report Human pluripotent stem cells (hPSCs) hold great promise for future applications in drug discovery and cell therapies. hPSC culture protocols require specific substrates and medium supplements to support cell expansion and lineage specific differentiation. The animal origin of these substrates is a severe limitation when considering the translation of hPSC derivatives to the clinic and in vitro disease modeling. The present study evaluates the use of a human placenta-derived extracellular matrix (ECM) hydrogel, HuGentra(Ⓡ), to support tri-lineage differentiation of human induced pluripotent stem cells (hiPSCs). Lineage-specific embryoid bodies (EBs) were plated onto three separate matrices, and differentiation efficiency was evaluated based on morphology, protein, and gene expression. HuGentra was found to support the differentiation of hiPSCs to all three germ layers: ectodermal, mesodermal, and endodermal lineages. hiPSCs differentiated into neurons, cardiomyocytes, and hepatocytes on HuGentra had similar morphology, protein, and gene expression compared to differentiation on Matrigel or other cell preferred matrices. HuGentra can be considered as a suitable human substrate for hiPSC differentiation. Korean Society for Stem Cell Research 2020-08-31 /pmc/articles/PMC7691852/ /pubmed/32840229 http://dx.doi.org/10.15283/ijsc20074 Text en Copyright © 2020 by the Korean Society for Stem Cell Research This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Report
Murchison, Angela C.
Odanga, Justin J.
Treadwell, Michelle L.
Breathwaite, Erick K.
Weaver, Jessica R.
Lee, Jung Bok
Human Placenta-Derived ECM Supports Tri-Lineage Differentiation of Human Induced Pluripotent Stem Cells
title Human Placenta-Derived ECM Supports Tri-Lineage Differentiation of Human Induced Pluripotent Stem Cells
title_full Human Placenta-Derived ECM Supports Tri-Lineage Differentiation of Human Induced Pluripotent Stem Cells
title_fullStr Human Placenta-Derived ECM Supports Tri-Lineage Differentiation of Human Induced Pluripotent Stem Cells
title_full_unstemmed Human Placenta-Derived ECM Supports Tri-Lineage Differentiation of Human Induced Pluripotent Stem Cells
title_short Human Placenta-Derived ECM Supports Tri-Lineage Differentiation of Human Induced Pluripotent Stem Cells
title_sort human placenta-derived ecm supports tri-lineage differentiation of human induced pluripotent stem cells
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691852/
https://www.ncbi.nlm.nih.gov/pubmed/32840229
http://dx.doi.org/10.15283/ijsc20074
work_keys_str_mv AT murchisonangelac humanplacentaderivedecmsupportstrilineagedifferentiationofhumaninducedpluripotentstemcells
AT odangajustinj humanplacentaderivedecmsupportstrilineagedifferentiationofhumaninducedpluripotentstemcells
AT treadwellmichellel humanplacentaderivedecmsupportstrilineagedifferentiationofhumaninducedpluripotentstemcells
AT breathwaiteerickk humanplacentaderivedecmsupportstrilineagedifferentiationofhumaninducedpluripotentstemcells
AT weaverjessicar humanplacentaderivedecmsupportstrilineagedifferentiationofhumaninducedpluripotentstemcells
AT leejungbok humanplacentaderivedecmsupportstrilineagedifferentiationofhumaninducedpluripotentstemcells