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Fabrication of biomimetic placental barrier structures within a microfluidic device utilizing two-photon polymerization

The placenta is a transient organ, essential for development and survival of the unborn fetus. It interfaces the body of the pregnant woman with the unborn child and secures transport of endogenous and exogenous substances. Maternal and fetal blood are thereby separated at any time, by the so-called...

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Autores principales: Mandt, Denise, Gruber, Peter, Markovic, Marica, Tromayer, Maximillian, Rothbauer, Mario, Kratz, Sebastian Rudi Adam, Ali, Syed Faheem, Hoorick, Jasper Van, Holnthoner, Wolfgang, Mühleder, Severin, Dubruel, Peter, Vlierberghe, Sandra Van, Ertl, Peter, Liska, Robert, Ovsianikov, Aleksandr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Whioce Publishing Pte. Ltd. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7581993/
https://www.ncbi.nlm.nih.gov/pubmed/33102920
http://dx.doi.org/10.18063/IJB.v4i2.144
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author Mandt, Denise
Gruber, Peter
Markovic, Marica
Tromayer, Maximillian
Rothbauer, Mario
Kratz, Sebastian Rudi Adam
Ali, Syed Faheem
Hoorick, Jasper Van
Holnthoner, Wolfgang
Mühleder, Severin
Dubruel, Peter
Vlierberghe, Sandra Van
Ertl, Peter
Liska, Robert
Ovsianikov, Aleksandr
author_facet Mandt, Denise
Gruber, Peter
Markovic, Marica
Tromayer, Maximillian
Rothbauer, Mario
Kratz, Sebastian Rudi Adam
Ali, Syed Faheem
Hoorick, Jasper Van
Holnthoner, Wolfgang
Mühleder, Severin
Dubruel, Peter
Vlierberghe, Sandra Van
Ertl, Peter
Liska, Robert
Ovsianikov, Aleksandr
author_sort Mandt, Denise
collection PubMed
description The placenta is a transient organ, essential for development and survival of the unborn fetus. It interfaces the body of the pregnant woman with the unborn child and secures transport of endogenous and exogenous substances. Maternal and fetal blood are thereby separated at any time, by the so-called placental barrier. Current in vitro approaches fail to model this multifaceted structure, therefore research in the field of placental biology is particularly challenging. The present study aimed at establishing a novel model, simulating placental transport and its implications on development, in a versatile but reproducible way. The basal membrane was replicated using a gelatin-based material, closely mimicking the composition and properties of the natural extracellular matrix. The microstructure was produced by using a high-resolution 3D printing method – the two-photon polymerization (2PP). In order to structure gelatin by 2PP, its primary amines and carboxylic acids are modified with methacrylamides and methacrylates (GelMOD-AEMA), respectively. High-resolution structures in the range of a few micrometers were produced within the intersection of a customized microfluidic device, separating the x-shaped chamber into two isolated cell culture compartments. Human umbilical-vein endothelial cells (HUVEC) seeded on one side of this membrane simulate the fetal compartment while human choriocarcinoma cells, isolated from placental tissue (BeWo B30) mimic the maternal syncytium. This barrier model in combination with native flow profiles can be used to mimic the microenvironment of the placenta, investigating different pharmaceutical, clinical and biological scenarios. As proof-of-principle, this bioengineered placental barrier was used for the investigation of transcellular transport processes. While high molecular weight substances did not permeate, smaller molecules in the size of glucose were able to diffuse through the barrier in a time-depended manner. We envision to apply this bioengineered placental barrier for pathophysiological research, where altered nutrient transport is associated with health risks for the fetus.
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spelling pubmed-75819932020-10-23 Fabrication of biomimetic placental barrier structures within a microfluidic device utilizing two-photon polymerization Mandt, Denise Gruber, Peter Markovic, Marica Tromayer, Maximillian Rothbauer, Mario Kratz, Sebastian Rudi Adam Ali, Syed Faheem Hoorick, Jasper Van Holnthoner, Wolfgang Mühleder, Severin Dubruel, Peter Vlierberghe, Sandra Van Ertl, Peter Liska, Robert Ovsianikov, Aleksandr Int J Bioprint Research Article The placenta is a transient organ, essential for development and survival of the unborn fetus. It interfaces the body of the pregnant woman with the unborn child and secures transport of endogenous and exogenous substances. Maternal and fetal blood are thereby separated at any time, by the so-called placental barrier. Current in vitro approaches fail to model this multifaceted structure, therefore research in the field of placental biology is particularly challenging. The present study aimed at establishing a novel model, simulating placental transport and its implications on development, in a versatile but reproducible way. The basal membrane was replicated using a gelatin-based material, closely mimicking the composition and properties of the natural extracellular matrix. The microstructure was produced by using a high-resolution 3D printing method – the two-photon polymerization (2PP). In order to structure gelatin by 2PP, its primary amines and carboxylic acids are modified with methacrylamides and methacrylates (GelMOD-AEMA), respectively. High-resolution structures in the range of a few micrometers were produced within the intersection of a customized microfluidic device, separating the x-shaped chamber into two isolated cell culture compartments. Human umbilical-vein endothelial cells (HUVEC) seeded on one side of this membrane simulate the fetal compartment while human choriocarcinoma cells, isolated from placental tissue (BeWo B30) mimic the maternal syncytium. This barrier model in combination with native flow profiles can be used to mimic the microenvironment of the placenta, investigating different pharmaceutical, clinical and biological scenarios. As proof-of-principle, this bioengineered placental barrier was used for the investigation of transcellular transport processes. While high molecular weight substances did not permeate, smaller molecules in the size of glucose were able to diffuse through the barrier in a time-depended manner. We envision to apply this bioengineered placental barrier for pathophysiological research, where altered nutrient transport is associated with health risks for the fetus. Whioce Publishing Pte. Ltd. 2018-07-03 /pmc/articles/PMC7581993/ /pubmed/33102920 http://dx.doi.org/10.18063/IJB.v4i2.144 Text en Copyright: © 2018 Mandt D, et al. http://creativecommons.org/licenses/cc-by-nc/4.0/ This is an open-access article distributed under the terms of the Attribution-NonCommercial 4.0 International 4.0 (CC BY-NC 4.0), which permits all non-commercial use, distribution, and reproduction in any medium provided the original work is properly cited.
spellingShingle Research Article
Mandt, Denise
Gruber, Peter
Markovic, Marica
Tromayer, Maximillian
Rothbauer, Mario
Kratz, Sebastian Rudi Adam
Ali, Syed Faheem
Hoorick, Jasper Van
Holnthoner, Wolfgang
Mühleder, Severin
Dubruel, Peter
Vlierberghe, Sandra Van
Ertl, Peter
Liska, Robert
Ovsianikov, Aleksandr
Fabrication of biomimetic placental barrier structures within a microfluidic device utilizing two-photon polymerization
title Fabrication of biomimetic placental barrier structures within a microfluidic device utilizing two-photon polymerization
title_full Fabrication of biomimetic placental barrier structures within a microfluidic device utilizing two-photon polymerization
title_fullStr Fabrication of biomimetic placental barrier structures within a microfluidic device utilizing two-photon polymerization
title_full_unstemmed Fabrication of biomimetic placental barrier structures within a microfluidic device utilizing two-photon polymerization
title_short Fabrication of biomimetic placental barrier structures within a microfluidic device utilizing two-photon polymerization
title_sort fabrication of biomimetic placental barrier structures within a microfluidic device utilizing two-photon polymerization
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7581993/
https://www.ncbi.nlm.nih.gov/pubmed/33102920
http://dx.doi.org/10.18063/IJB.v4i2.144
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