Topographic Guidance in Melt-Electrowritten Tubular Scaffolds Enhances Engineered Kidney Tubule Performance
Introduction: To date, tubular tissue engineering relies on large, non-porous tubular scaffolds (Ø > 2 mm) for mechanical self-support, or smaller (Ø 150–500 μm) tubes within bulk hydrogels for studying renal transport phenomena. To advance the engineering of kidney tubules for future implant...
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Format: | Article |
Language: | English |
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Frontiers Media S.A.
2021-01-01
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Series: | Frontiers in Bioengineering and Biotechnology |
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Online Access: | https://www.frontiersin.org/articles/10.3389/fbioe.2020.617364/full |
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doaj-0026f416d5904a9f9f259f6f8910b759 |
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record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Anne Metje van Genderen Katja Jansen Marleen Kristen Marleen Kristen Joost van Duijn Joost van Duijn Yang Li Yang Li Carl C. L. Schuurmans Carl C. L. Schuurmans Jos Malda Jos Malda Jos Malda Tina Vermonden Tina Vermonden Jitske Jansen Rosalinde Masereeuw Rosalinde Masereeuw Miguel Castilho Miguel Castilho Miguel Castilho |
spellingShingle |
Anne Metje van Genderen Katja Jansen Marleen Kristen Marleen Kristen Joost van Duijn Joost van Duijn Yang Li Yang Li Carl C. L. Schuurmans Carl C. L. Schuurmans Jos Malda Jos Malda Jos Malda Tina Vermonden Tina Vermonden Jitske Jansen Rosalinde Masereeuw Rosalinde Masereeuw Miguel Castilho Miguel Castilho Miguel Castilho Topographic Guidance in Melt-Electrowritten Tubular Scaffolds Enhances Engineered Kidney Tubule Performance Frontiers in Bioengineering and Biotechnology tissue engineering melt-electrowriting bioartificial kidney contact guidance 3D culture |
author_facet |
Anne Metje van Genderen Katja Jansen Marleen Kristen Marleen Kristen Joost van Duijn Joost van Duijn Yang Li Yang Li Carl C. L. Schuurmans Carl C. L. Schuurmans Jos Malda Jos Malda Jos Malda Tina Vermonden Tina Vermonden Jitske Jansen Rosalinde Masereeuw Rosalinde Masereeuw Miguel Castilho Miguel Castilho Miguel Castilho |
author_sort |
Anne Metje van Genderen |
title |
Topographic Guidance in Melt-Electrowritten Tubular Scaffolds Enhances Engineered Kidney Tubule Performance |
title_short |
Topographic Guidance in Melt-Electrowritten Tubular Scaffolds Enhances Engineered Kidney Tubule Performance |
title_full |
Topographic Guidance in Melt-Electrowritten Tubular Scaffolds Enhances Engineered Kidney Tubule Performance |
title_fullStr |
Topographic Guidance in Melt-Electrowritten Tubular Scaffolds Enhances Engineered Kidney Tubule Performance |
title_full_unstemmed |
Topographic Guidance in Melt-Electrowritten Tubular Scaffolds Enhances Engineered Kidney Tubule Performance |
title_sort |
topographic guidance in melt-electrowritten tubular scaffolds enhances engineered kidney tubule performance |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Bioengineering and Biotechnology |
issn |
2296-4185 |
publishDate |
2021-01-01 |
description |
Introduction: To date, tubular tissue engineering relies on large, non-porous tubular scaffolds (Ø > 2 mm) for mechanical self-support, or smaller (Ø 150–500 μm) tubes within bulk hydrogels for studying renal transport phenomena. To advance the engineering of kidney tubules for future implantation, constructs should be both self-supportive and yet small-sized and highly porous. Here, we hypothesize that the fabrication of small-sized porous tubular scaffolds with a highly organized fibrous microstructure by means of melt-electrowriting (MEW) allows the development of self-supported kidney proximal tubules with enhanced properties.Materials and Methods: A custom-built melt-electrowriting (MEW) device was used to fabricate tubular fibrous scaffolds with small diameter sizes (Ø = 0.5, 1, 3 mm) and well-defined, porous microarchitectures (rhombus, square, and random). Human umbilical vein endothelial cells (HUVEC) and human conditionally immortalized proximal tubular epithelial cells (ciPTEC) were seeded into the tubular scaffolds and tested for monolayer formation, integrity, and organization, as well as for extracellular matrix (ECM) production and renal transport functionality.Results: Tubular fibrous scaffolds were successfully manufactured by fine control of MEW instrument parameters. A minimum inner diameter of 1 mm and pore sizes of 0.2 mm were achieved and used for subsequent cell experiments. While HUVEC were unable to bridge the pores, ciPTEC formed tight monolayers in all scaffold microarchitectures tested. Well-defined rhombus-shaped pores outperformed and facilitated unidirectional cell orientation, increased collagen type IV deposition, and expression of the renal transporters and differentiation markers organic cation transporter 2 (OCT2) and P-glycoprotein (P-gp).Discussion and Conclusion: Here, we present smaller diameter engineered kidney tubules with microgeometry-directed cell functionality. Due to the well-organized tubular fiber scaffold microstructure, the tubes are mechanically self-supported, and the self-produced ECM constitutes the only barrier between the inner and outer compartment, facilitating rapid and active solute transport. |
topic |
tissue engineering melt-electrowriting bioartificial kidney contact guidance 3D culture |
url |
https://www.frontiersin.org/articles/10.3389/fbioe.2020.617364/full |
work_keys_str_mv |
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doaj-0026f416d5904a9f9f259f6f8910b7592021-01-18T05:27:04ZengFrontiers Media S.A.Frontiers in Bioengineering and Biotechnology2296-41852021-01-01810.3389/fbioe.2020.617364617364Topographic Guidance in Melt-Electrowritten Tubular Scaffolds Enhances Engineered Kidney Tubule PerformanceAnne Metje van Genderen0Katja Jansen1Marleen Kristen2Marleen Kristen3Joost van Duijn4Joost van Duijn5Yang Li6Yang Li7Carl C. L. Schuurmans8Carl C. L. Schuurmans9Jos Malda10Jos Malda11Jos Malda12Tina Vermonden13Tina Vermonden14Jitske Jansen15Rosalinde Masereeuw16Rosalinde Masereeuw17Miguel Castilho18Miguel Castilho19Miguel Castilho20Division of Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Utrecht, NetherlandsDivision of Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Utrecht, NetherlandsDivision of Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Utrecht, NetherlandsDepartment of Orthopaedics, University Medical Center Utrecht, Utrecht University, Utrecht, NetherlandsDepartment of Orthopaedics, University Medical Center Utrecht, Utrecht University, Utrecht, NetherlandsRegenerative Medicine Center Utrecht, University Medical Center Utrecht, Utrecht, NetherlandsDepartment of Orthopaedics, University Medical Center Utrecht, Utrecht University, Utrecht, NetherlandsRegenerative Medicine Center Utrecht, University Medical Center Utrecht, Utrecht, NetherlandsDivision of Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Utrecht, NetherlandsDivision of Pharmaceutics, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Utrecht, NetherlandsDepartment of Orthopaedics, University Medical Center Utrecht, Utrecht University, Utrecht, NetherlandsRegenerative Medicine Center Utrecht, University Medical Center Utrecht, Utrecht, NetherlandsDepartment of Clinical Sciences, Faculty of Veterinary Medicine, Utrecht University, Utrecht, NetherlandsRegenerative Medicine Center Utrecht, University Medical Center Utrecht, Utrecht, NetherlandsDivision of Pharmaceutics, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Utrecht, NetherlandsDepartment of Pathology and Pediatric Nephrology, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, NetherlandsDivision of Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Utrecht, NetherlandsRegenerative Medicine Center Utrecht, University Medical Center Utrecht, Utrecht, NetherlandsDepartment of Orthopaedics, University Medical Center Utrecht, Utrecht University, Utrecht, NetherlandsRegenerative Medicine Center Utrecht, University Medical Center Utrecht, Utrecht, NetherlandsDepartment of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, NetherlandsIntroduction: To date, tubular tissue engineering relies on large, non-porous tubular scaffolds (Ø > 2 mm) for mechanical self-support, or smaller (Ø 150–500 μm) tubes within bulk hydrogels for studying renal transport phenomena. To advance the engineering of kidney tubules for future implantation, constructs should be both self-supportive and yet small-sized and highly porous. Here, we hypothesize that the fabrication of small-sized porous tubular scaffolds with a highly organized fibrous microstructure by means of melt-electrowriting (MEW) allows the development of self-supported kidney proximal tubules with enhanced properties.Materials and Methods: A custom-built melt-electrowriting (MEW) device was used to fabricate tubular fibrous scaffolds with small diameter sizes (Ø = 0.5, 1, 3 mm) and well-defined, porous microarchitectures (rhombus, square, and random). Human umbilical vein endothelial cells (HUVEC) and human conditionally immortalized proximal tubular epithelial cells (ciPTEC) were seeded into the tubular scaffolds and tested for monolayer formation, integrity, and organization, as well as for extracellular matrix (ECM) production and renal transport functionality.Results: Tubular fibrous scaffolds were successfully manufactured by fine control of MEW instrument parameters. A minimum inner diameter of 1 mm and pore sizes of 0.2 mm were achieved and used for subsequent cell experiments. While HUVEC were unable to bridge the pores, ciPTEC formed tight monolayers in all scaffold microarchitectures tested. Well-defined rhombus-shaped pores outperformed and facilitated unidirectional cell orientation, increased collagen type IV deposition, and expression of the renal transporters and differentiation markers organic cation transporter 2 (OCT2) and P-glycoprotein (P-gp).Discussion and Conclusion: Here, we present smaller diameter engineered kidney tubules with microgeometry-directed cell functionality. Due to the well-organized tubular fiber scaffold microstructure, the tubes are mechanically self-supported, and the self-produced ECM constitutes the only barrier between the inner and outer compartment, facilitating rapid and active solute transport.https://www.frontiersin.org/articles/10.3389/fbioe.2020.617364/fulltissue engineeringmelt-electrowritingbioartificial kidneycontact guidance3D culture |