Cargando…
Epithelial differentiation of human adipose-derived stem cells (hASCs) undergoing three-dimensional (3D) cultivation with collagen sponge scaffold (CSS) via an indirect co-culture strategy
BACKGROUND: Three-dimensional (3D) cultivation with biomaterials was proposed to facilitate stem cell epithelial differentiation for wound healing. However, whether human adipose-derived stem cells (hASCs) on collagen sponge scaffold (CSS) better differentiate to keratinocytes remains unclear. METHO...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7110797/ https://www.ncbi.nlm.nih.gov/pubmed/32234069 http://dx.doi.org/10.1186/s13287-020-01645-3 |
_version_ | 1783513138433359872 |
---|---|
author | Li, Minxiong Ma, Jun Gao, Yanbin Dong, Mengru Zheng, Zijun Li, Yuchen Tan, Rongwei She, Zhending Yang, Lei |
author_facet | Li, Minxiong Ma, Jun Gao, Yanbin Dong, Mengru Zheng, Zijun Li, Yuchen Tan, Rongwei She, Zhending Yang, Lei |
author_sort | Li, Minxiong |
collection | PubMed |
description | BACKGROUND: Three-dimensional (3D) cultivation with biomaterials was proposed to facilitate stem cell epithelial differentiation for wound healing. However, whether human adipose-derived stem cells (hASCs) on collagen sponge scaffold (CSS) better differentiate to keratinocytes remains unclear. METHODS: 3D cultivation with CSS on hASC epidermal differentiation co-cultured with HaCaT cells at air-liquid interface (ALI) was compared with two-dimensional (2D) form and cultivation without “co-culture” or “ALI.” Cellular morphology, cell adhesion, and growth condition were evaluated, followed by the protein and gene expression of keratin 14 (K14, keratinocyte specific marker). RESULTS: Typical cobblestone morphology of keratinocytes was remarkably observed in co-cultured hASCs at ALI, but those seeded on the CSS exhibited more keratinocyte-like cells under an invert microscope and scanning electron microscope. Desired cell adhesion and proliferation were confirmed in 3D differentiation groups by rhodamine-labeled phalloidin staining, consistent with H&E staining. Compared with those cultured in 2D culture system or without “ALI,” immunofluorescence staining and gene expression analysis revealed hASCs co-cultured over CSS expressed K14 at higher levels at day 15. CONCLUSIONS: CSS is positive to promote epithelial differentiation of hASCs, which will foster a deeper understanding of artificial dermis in skin wound healing and regeneration. |
format | Online Article Text |
id | pubmed-7110797 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-71107972020-04-07 Epithelial differentiation of human adipose-derived stem cells (hASCs) undergoing three-dimensional (3D) cultivation with collagen sponge scaffold (CSS) via an indirect co-culture strategy Li, Minxiong Ma, Jun Gao, Yanbin Dong, Mengru Zheng, Zijun Li, Yuchen Tan, Rongwei She, Zhending Yang, Lei Stem Cell Res Ther Research BACKGROUND: Three-dimensional (3D) cultivation with biomaterials was proposed to facilitate stem cell epithelial differentiation for wound healing. However, whether human adipose-derived stem cells (hASCs) on collagen sponge scaffold (CSS) better differentiate to keratinocytes remains unclear. METHODS: 3D cultivation with CSS on hASC epidermal differentiation co-cultured with HaCaT cells at air-liquid interface (ALI) was compared with two-dimensional (2D) form and cultivation without “co-culture” or “ALI.” Cellular morphology, cell adhesion, and growth condition were evaluated, followed by the protein and gene expression of keratin 14 (K14, keratinocyte specific marker). RESULTS: Typical cobblestone morphology of keratinocytes was remarkably observed in co-cultured hASCs at ALI, but those seeded on the CSS exhibited more keratinocyte-like cells under an invert microscope and scanning electron microscope. Desired cell adhesion and proliferation were confirmed in 3D differentiation groups by rhodamine-labeled phalloidin staining, consistent with H&E staining. Compared with those cultured in 2D culture system or without “ALI,” immunofluorescence staining and gene expression analysis revealed hASCs co-cultured over CSS expressed K14 at higher levels at day 15. CONCLUSIONS: CSS is positive to promote epithelial differentiation of hASCs, which will foster a deeper understanding of artificial dermis in skin wound healing and regeneration. BioMed Central 2020-03-31 /pmc/articles/PMC7110797/ /pubmed/32234069 http://dx.doi.org/10.1186/s13287-020-01645-3 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Li, Minxiong Ma, Jun Gao, Yanbin Dong, Mengru Zheng, Zijun Li, Yuchen Tan, Rongwei She, Zhending Yang, Lei Epithelial differentiation of human adipose-derived stem cells (hASCs) undergoing three-dimensional (3D) cultivation with collagen sponge scaffold (CSS) via an indirect co-culture strategy |
title | Epithelial differentiation of human adipose-derived stem cells (hASCs) undergoing three-dimensional (3D) cultivation with collagen sponge scaffold (CSS) via an indirect co-culture strategy |
title_full | Epithelial differentiation of human adipose-derived stem cells (hASCs) undergoing three-dimensional (3D) cultivation with collagen sponge scaffold (CSS) via an indirect co-culture strategy |
title_fullStr | Epithelial differentiation of human adipose-derived stem cells (hASCs) undergoing three-dimensional (3D) cultivation with collagen sponge scaffold (CSS) via an indirect co-culture strategy |
title_full_unstemmed | Epithelial differentiation of human adipose-derived stem cells (hASCs) undergoing three-dimensional (3D) cultivation with collagen sponge scaffold (CSS) via an indirect co-culture strategy |
title_short | Epithelial differentiation of human adipose-derived stem cells (hASCs) undergoing three-dimensional (3D) cultivation with collagen sponge scaffold (CSS) via an indirect co-culture strategy |
title_sort | epithelial differentiation of human adipose-derived stem cells (hascs) undergoing three-dimensional (3d) cultivation with collagen sponge scaffold (css) via an indirect co-culture strategy |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7110797/ https://www.ncbi.nlm.nih.gov/pubmed/32234069 http://dx.doi.org/10.1186/s13287-020-01645-3 |
work_keys_str_mv | AT liminxiong epithelialdifferentiationofhumanadiposederivedstemcellshascsundergoingthreedimensional3dcultivationwithcollagenspongescaffoldcssviaanindirectcoculturestrategy AT majun epithelialdifferentiationofhumanadiposederivedstemcellshascsundergoingthreedimensional3dcultivationwithcollagenspongescaffoldcssviaanindirectcoculturestrategy AT gaoyanbin epithelialdifferentiationofhumanadiposederivedstemcellshascsundergoingthreedimensional3dcultivationwithcollagenspongescaffoldcssviaanindirectcoculturestrategy AT dongmengru epithelialdifferentiationofhumanadiposederivedstemcellshascsundergoingthreedimensional3dcultivationwithcollagenspongescaffoldcssviaanindirectcoculturestrategy AT zhengzijun epithelialdifferentiationofhumanadiposederivedstemcellshascsundergoingthreedimensional3dcultivationwithcollagenspongescaffoldcssviaanindirectcoculturestrategy AT liyuchen epithelialdifferentiationofhumanadiposederivedstemcellshascsundergoingthreedimensional3dcultivationwithcollagenspongescaffoldcssviaanindirectcoculturestrategy AT tanrongwei epithelialdifferentiationofhumanadiposederivedstemcellshascsundergoingthreedimensional3dcultivationwithcollagenspongescaffoldcssviaanindirectcoculturestrategy AT shezhending epithelialdifferentiationofhumanadiposederivedstemcellshascsundergoingthreedimensional3dcultivationwithcollagenspongescaffoldcssviaanindirectcoculturestrategy AT yanglei epithelialdifferentiationofhumanadiposederivedstemcellshascsundergoingthreedimensional3dcultivationwithcollagenspongescaffoldcssviaanindirectcoculturestrategy |