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...
Autores principales: | , , , , , |
---|---|
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 |