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Microscopy‐guided laser ablation for the creation of complex skin models with folliculoid appendages

Engineering complex tissues requires the use of advanced biofabrication techniques that allow the replication of the tissue's 3D microenvironment, architecture and cellular interactions. In the case of skin, the most successful strategies to introduce the complexity of hair follicle (HF) append...

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Autores principales: Abreu, Carla M., Gasperini, Luca, Lago, Manuela E. L., Reis, Rui L., Marques, Alexandra P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8126819/
https://www.ncbi.nlm.nih.gov/pubmed/34027085
http://dx.doi.org/10.1002/btm2.10195
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author Abreu, Carla M.
Gasperini, Luca
Lago, Manuela E. L.
Reis, Rui L.
Marques, Alexandra P.
author_facet Abreu, Carla M.
Gasperini, Luca
Lago, Manuela E. L.
Reis, Rui L.
Marques, Alexandra P.
author_sort Abreu, Carla M.
collection PubMed
description Engineering complex tissues requires the use of advanced biofabrication techniques that allow the replication of the tissue's 3D microenvironment, architecture and cellular interactions. In the case of skin, the most successful strategies to introduce the complexity of hair follicle (HF) appendages have highlighted the importance of facilitating direct interaction between dermal papilla (DP) cells and keratinocytes (KCs) in organotypic skin models. In this work, we took advantage of microscopy‐guided laser ablation (MGLA) to microfabricate a fibroblast‐populated collagen hydrogel and create a subcompartment that guides the migration of KCs and lead their interaction with DP cells to recreate follicular structures. Upon definition of the processing parameters (laser incidence area and power), MGLA was used to create 3D microchannels from the surface of a standard organotypic human skin model up to the aggregates containing DP cells and KCs, previously incorporated into the dermal‐like fibroblast‐collagen layer. Analysis of the constructs showed that the fabricated microfeatures successfully guided the fusion between epidermal and aggregates keratinocytes, which differentiated into follicular‐like structures within the organotypic human skin model, increasing its functionality. In summary, we demonstrate the fabrication of a highly structured 3D hydrogel‐based construct using MGLA to attain a complex skin model bearing folliculoid structures, highlighting its potential use as an in vitro platform to study the mechanisms controlling HF development or for the screening of bioactive substances.
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spelling pubmed-81268192021-05-21 Microscopy‐guided laser ablation for the creation of complex skin models with folliculoid appendages Abreu, Carla M. Gasperini, Luca Lago, Manuela E. L. Reis, Rui L. Marques, Alexandra P. Bioeng Transl Med Rapid Communication Engineering complex tissues requires the use of advanced biofabrication techniques that allow the replication of the tissue's 3D microenvironment, architecture and cellular interactions. In the case of skin, the most successful strategies to introduce the complexity of hair follicle (HF) appendages have highlighted the importance of facilitating direct interaction between dermal papilla (DP) cells and keratinocytes (KCs) in organotypic skin models. In this work, we took advantage of microscopy‐guided laser ablation (MGLA) to microfabricate a fibroblast‐populated collagen hydrogel and create a subcompartment that guides the migration of KCs and lead their interaction with DP cells to recreate follicular structures. Upon definition of the processing parameters (laser incidence area and power), MGLA was used to create 3D microchannels from the surface of a standard organotypic human skin model up to the aggregates containing DP cells and KCs, previously incorporated into the dermal‐like fibroblast‐collagen layer. Analysis of the constructs showed that the fabricated microfeatures successfully guided the fusion between epidermal and aggregates keratinocytes, which differentiated into follicular‐like structures within the organotypic human skin model, increasing its functionality. In summary, we demonstrate the fabrication of a highly structured 3D hydrogel‐based construct using MGLA to attain a complex skin model bearing folliculoid structures, highlighting its potential use as an in vitro platform to study the mechanisms controlling HF development or for the screening of bioactive substances. John Wiley & Sons, Inc. 2020-12-15 /pmc/articles/PMC8126819/ /pubmed/34027085 http://dx.doi.org/10.1002/btm2.10195 Text en © 2020 The Authors. Bioengineering & Translational Medicine published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Rapid Communication
Abreu, Carla M.
Gasperini, Luca
Lago, Manuela E. L.
Reis, Rui L.
Marques, Alexandra P.
Microscopy‐guided laser ablation for the creation of complex skin models with folliculoid appendages
title Microscopy‐guided laser ablation for the creation of complex skin models with folliculoid appendages
title_full Microscopy‐guided laser ablation for the creation of complex skin models with folliculoid appendages
title_fullStr Microscopy‐guided laser ablation for the creation of complex skin models with folliculoid appendages
title_full_unstemmed Microscopy‐guided laser ablation for the creation of complex skin models with folliculoid appendages
title_short Microscopy‐guided laser ablation for the creation of complex skin models with folliculoid appendages
title_sort microscopy‐guided laser ablation for the creation of complex skin models with folliculoid appendages
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8126819/
https://www.ncbi.nlm.nih.gov/pubmed/34027085
http://dx.doi.org/10.1002/btm2.10195
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