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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Main Authors: Anne Metje van Genderen, Katja Jansen, Marleen Kristen, Joost van Duijn, Yang Li, Carl C. L. Schuurmans, Jos Malda, Tina Vermonden, Jitske Jansen, Rosalinde Masereeuw, Miguel Castilho
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-01-01
Series:Frontiers in Bioengineering and Biotechnology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fbioe.2020.617364/full
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language English
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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
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spelling 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