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An Engineered Infected Epidermis Model for In Vitro Study of the Skin’s Pro-Inflammatory Response

Wound infection is a major clinical challenge that can significantly delay the healing process, can create pain, and requires prolonged hospital stays. Pre-clinical research to evaluate new drugs normally involves animals. However, ethical concerns, cost, and the challenges associated with interspec...

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Autores principales: Jahanshahi, Maryam, Hamdi, David, Godau, Brent, Samiei, Ehsan, Sanchez-Lafuente, Carla Liria, Neale, Katie J., Hadisi, Zhina, Dabiri, Seyed Mohammad Hossein, Pagan, Erik, Christie, Brian R., Akbari, Mohsen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074829/
https://www.ncbi.nlm.nih.gov/pubmed/32102205
http://dx.doi.org/10.3390/mi11020227
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author Jahanshahi, Maryam
Hamdi, David
Godau, Brent
Samiei, Ehsan
Sanchez-Lafuente, Carla Liria
Neale, Katie J.
Hadisi, Zhina
Dabiri, Seyed Mohammad Hossein
Pagan, Erik
Christie, Brian R.
Akbari, Mohsen
author_facet Jahanshahi, Maryam
Hamdi, David
Godau, Brent
Samiei, Ehsan
Sanchez-Lafuente, Carla Liria
Neale, Katie J.
Hadisi, Zhina
Dabiri, Seyed Mohammad Hossein
Pagan, Erik
Christie, Brian R.
Akbari, Mohsen
author_sort Jahanshahi, Maryam
collection PubMed
description Wound infection is a major clinical challenge that can significantly delay the healing process, can create pain, and requires prolonged hospital stays. Pre-clinical research to evaluate new drugs normally involves animals. However, ethical concerns, cost, and the challenges associated with interspecies variation remain major obstacles. Tissue engineering enables the development of in vitro human skin models for drug testing. However, existing engineered skin models are representative of healthy human skin and its normal functions. This paper presents a functional infected epidermis model that consists of a multilayer epidermis structure formed at an air-liquid interface on a hydrogel matrix and a three-dimensionally (3D) printed vascular-like network. The function of the engineered epidermis is evaluated by the expression of the terminal differentiation marker, filaggrin, and the barrier function of the epidermis model using the electrical resistance and permeability across the epidermal layer. The results showed that the multilayer structure enhances the electrical resistance by 40% and decreased the drug permeation by 16.9% in the epidermis model compared to the monolayer cell culture on gelatin. We infect the model with Escherichia coli to study the inflammatory response of keratinocytes by measuring the expression level of pro-inflammatory cytokines (interleukin 1 beta and tumor necrosis factor alpha). After 24 h of exposure to Escherichia coli, the level of IL-1β and TNF-α in control samples were 125 ± 78 and 920 ± 187 pg/mL respectively, while in infected samples, they were 1429 ± 101 and 2155.5 ± 279 pg/mL respectively. However, in ciprofloxacin-treated samples the levels of IL-1β and TNF-α without significant difference with respect to the control reached to 246 ± 87 and 1141.5 ± 97 pg/mL respectively. The robust fabrication procedure and functionality of this model suggest that the model has great potential for modeling wound infections and drug testing.
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spelling pubmed-70748292020-03-20 An Engineered Infected Epidermis Model for In Vitro Study of the Skin’s Pro-Inflammatory Response Jahanshahi, Maryam Hamdi, David Godau, Brent Samiei, Ehsan Sanchez-Lafuente, Carla Liria Neale, Katie J. Hadisi, Zhina Dabiri, Seyed Mohammad Hossein Pagan, Erik Christie, Brian R. Akbari, Mohsen Micromachines (Basel) Article Wound infection is a major clinical challenge that can significantly delay the healing process, can create pain, and requires prolonged hospital stays. Pre-clinical research to evaluate new drugs normally involves animals. However, ethical concerns, cost, and the challenges associated with interspecies variation remain major obstacles. Tissue engineering enables the development of in vitro human skin models for drug testing. However, existing engineered skin models are representative of healthy human skin and its normal functions. This paper presents a functional infected epidermis model that consists of a multilayer epidermis structure formed at an air-liquid interface on a hydrogel matrix and a three-dimensionally (3D) printed vascular-like network. The function of the engineered epidermis is evaluated by the expression of the terminal differentiation marker, filaggrin, and the barrier function of the epidermis model using the electrical resistance and permeability across the epidermal layer. The results showed that the multilayer structure enhances the electrical resistance by 40% and decreased the drug permeation by 16.9% in the epidermis model compared to the monolayer cell culture on gelatin. We infect the model with Escherichia coli to study the inflammatory response of keratinocytes by measuring the expression level of pro-inflammatory cytokines (interleukin 1 beta and tumor necrosis factor alpha). After 24 h of exposure to Escherichia coli, the level of IL-1β and TNF-α in control samples were 125 ± 78 and 920 ± 187 pg/mL respectively, while in infected samples, they were 1429 ± 101 and 2155.5 ± 279 pg/mL respectively. However, in ciprofloxacin-treated samples the levels of IL-1β and TNF-α without significant difference with respect to the control reached to 246 ± 87 and 1141.5 ± 97 pg/mL respectively. The robust fabrication procedure and functionality of this model suggest that the model has great potential for modeling wound infections and drug testing. MDPI 2020-02-23 /pmc/articles/PMC7074829/ /pubmed/32102205 http://dx.doi.org/10.3390/mi11020227 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
Jahanshahi, Maryam
Hamdi, David
Godau, Brent
Samiei, Ehsan
Sanchez-Lafuente, Carla Liria
Neale, Katie J.
Hadisi, Zhina
Dabiri, Seyed Mohammad Hossein
Pagan, Erik
Christie, Brian R.
Akbari, Mohsen
An Engineered Infected Epidermis Model for In Vitro Study of the Skin’s Pro-Inflammatory Response
title An Engineered Infected Epidermis Model for In Vitro Study of the Skin’s Pro-Inflammatory Response
title_full An Engineered Infected Epidermis Model for In Vitro Study of the Skin’s Pro-Inflammatory Response
title_fullStr An Engineered Infected Epidermis Model for In Vitro Study of the Skin’s Pro-Inflammatory Response
title_full_unstemmed An Engineered Infected Epidermis Model for In Vitro Study of the Skin’s Pro-Inflammatory Response
title_short An Engineered Infected Epidermis Model for In Vitro Study of the Skin’s Pro-Inflammatory Response
title_sort engineered infected epidermis model for in vitro study of the skin’s pro-inflammatory response
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074829/
https://www.ncbi.nlm.nih.gov/pubmed/32102205
http://dx.doi.org/10.3390/mi11020227
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