Cargando…
Topography-Mediated Myotube and Endothelial Alignment, Differentiation, and Extracellular Matrix Organization for Skeletal Muscle Engineering
Understanding the response of endothelial cells to aligned myotubes is important to create an appropriate environment for tissue-engineered vascularized skeletal muscle. Part of the native tissue environment is the extracellular matrix (ECM). The ECM is a supportive scaffold for cells and allows cel...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7564871/ https://www.ncbi.nlm.nih.gov/pubmed/32872193 http://dx.doi.org/10.3390/polym12091948 |
_version_ | 1783595812373135360 |
---|---|
author | Almonacid Suarez, Ana Maria Brinker, Marja G. L. Brouwer, Linda A. van der Ham, Iris Harmsen, Martin C. van Rijn, Patrick |
author_facet | Almonacid Suarez, Ana Maria Brinker, Marja G. L. Brouwer, Linda A. van der Ham, Iris Harmsen, Martin C. van Rijn, Patrick |
author_sort | Almonacid Suarez, Ana Maria |
collection | PubMed |
description | Understanding the response of endothelial cells to aligned myotubes is important to create an appropriate environment for tissue-engineered vascularized skeletal muscle. Part of the native tissue environment is the extracellular matrix (ECM). The ECM is a supportive scaffold for cells and allows cellular processes such as proliferation, differentiation, and migration. Interstitial matrix and basal membrane both comprise proteinaceous and polysaccharide components for strength, architecture, and volume retention. Virtually all cells are anchored to their basal lamina. One of the physical factors that affects cell behavior is topography, which plays an important role on cell alignment. We tested the hypothesis that topography-driven aligned human myotubes promote and support vascular network formation as a prelude to in vitro engineered vascularized skeletal muscle. Therefore, we used a PDMS-based topography substrate to investigate the influence of pre-aligned myotubes on the network formation of microvascular endothelial cells. The aligned myotubes produced a network of collagen fibers and laminin. This network supported early stages of endothelial network formation. |
format | Online Article Text |
id | pubmed-7564871 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75648712020-10-26 Topography-Mediated Myotube and Endothelial Alignment, Differentiation, and Extracellular Matrix Organization for Skeletal Muscle Engineering Almonacid Suarez, Ana Maria Brinker, Marja G. L. Brouwer, Linda A. van der Ham, Iris Harmsen, Martin C. van Rijn, Patrick Polymers (Basel) Article Understanding the response of endothelial cells to aligned myotubes is important to create an appropriate environment for tissue-engineered vascularized skeletal muscle. Part of the native tissue environment is the extracellular matrix (ECM). The ECM is a supportive scaffold for cells and allows cellular processes such as proliferation, differentiation, and migration. Interstitial matrix and basal membrane both comprise proteinaceous and polysaccharide components for strength, architecture, and volume retention. Virtually all cells are anchored to their basal lamina. One of the physical factors that affects cell behavior is topography, which plays an important role on cell alignment. We tested the hypothesis that topography-driven aligned human myotubes promote and support vascular network formation as a prelude to in vitro engineered vascularized skeletal muscle. Therefore, we used a PDMS-based topography substrate to investigate the influence of pre-aligned myotubes on the network formation of microvascular endothelial cells. The aligned myotubes produced a network of collagen fibers and laminin. This network supported early stages of endothelial network formation. MDPI 2020-08-28 /pmc/articles/PMC7564871/ /pubmed/32872193 http://dx.doi.org/10.3390/polym12091948 Text en © 2020 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 Almonacid Suarez, Ana Maria Brinker, Marja G. L. Brouwer, Linda A. van der Ham, Iris Harmsen, Martin C. van Rijn, Patrick Topography-Mediated Myotube and Endothelial Alignment, Differentiation, and Extracellular Matrix Organization for Skeletal Muscle Engineering |
title | Topography-Mediated Myotube and Endothelial Alignment, Differentiation, and Extracellular Matrix Organization for Skeletal Muscle Engineering |
title_full | Topography-Mediated Myotube and Endothelial Alignment, Differentiation, and Extracellular Matrix Organization for Skeletal Muscle Engineering |
title_fullStr | Topography-Mediated Myotube and Endothelial Alignment, Differentiation, and Extracellular Matrix Organization for Skeletal Muscle Engineering |
title_full_unstemmed | Topography-Mediated Myotube and Endothelial Alignment, Differentiation, and Extracellular Matrix Organization for Skeletal Muscle Engineering |
title_short | Topography-Mediated Myotube and Endothelial Alignment, Differentiation, and Extracellular Matrix Organization for Skeletal Muscle Engineering |
title_sort | topography-mediated myotube and endothelial alignment, differentiation, and extracellular matrix organization for skeletal muscle engineering |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7564871/ https://www.ncbi.nlm.nih.gov/pubmed/32872193 http://dx.doi.org/10.3390/polym12091948 |
work_keys_str_mv | AT almonacidsuarezanamaria topographymediatedmyotubeandendothelialalignmentdifferentiationandextracellularmatrixorganizationforskeletalmuscleengineering AT brinkermarjagl topographymediatedmyotubeandendothelialalignmentdifferentiationandextracellularmatrixorganizationforskeletalmuscleengineering AT brouwerlindaa topographymediatedmyotubeandendothelialalignmentdifferentiationandextracellularmatrixorganizationforskeletalmuscleengineering AT vanderhamiris topographymediatedmyotubeandendothelialalignmentdifferentiationandextracellularmatrixorganizationforskeletalmuscleengineering AT harmsenmartinc topographymediatedmyotubeandendothelialalignmentdifferentiationandextracellularmatrixorganizationforskeletalmuscleengineering AT vanrijnpatrick topographymediatedmyotubeandendothelialalignmentdifferentiationandextracellularmatrixorganizationforskeletalmuscleengineering |