TY - JOUR
T1 - Thermoforming for Small Feature Replication in Melt Electrowritten Membranes to Model Kidney Proximal Tubule
AU - G Valverde, Marta
AU - Stampa Zamorano, Claudia
AU - Kožinec, Dora
AU - Benito Zarza, Laura
AU - van Genderen, Anne Metje
AU - Janssen, Robine
AU - Castilho, Miguel
AU - Hrynevich, Andrei
AU - Vermonden, Tina
AU - Malda, Jos
AU - de Ruijter, Mylene
AU - Masereeuw, Rosalinde
AU - Mihăilă, Silvia M.
N1 - Publisher Copyright:
© 2024 The Author(s). Advanced Healthcare Materials published by Wiley-VCH GmbH.
PY - 2025/1/3
Y1 - 2025/1/3
N2 - A novel approach merging melt electrowriting (MEW) with matched die thermoforming to achieve scaffolds with micron-sized curvatures (200 – 800 µm versus 1000 µm of mandrel printing) for in vitro modeling of the kidney proximal tubule (PT) is proposed. Recent advances in this field emphasize the relevance of accurately replicating the intricate tissue microenvironment, particularly the curvature of the nephrons’ tubular segments. While MEW offers promising capabilities for fabricating highly and porous precise 3D structures mimicking the PT, challenges persist in approximating the diameter of tubular scaffolds to match the actual PT. The thermoformed MEW membranes retain the initial MEW printing design parameters (rhombus geometry, porosity > 45%) while accurately following the imprinted curvature (ratios between 0.67-0.95). PT epithelial cells cultured on these membranes demonstrate the ability to fill in the large pores of the membrane by secreting their own collagen IV-rich extracellular matrix and form an organized, functional, and tight monolayer expressing characteristic PT markers. Besides approximating PT architecture, this setup maximizes the usable surface area for cell culture and molecular readouts. By closely mimicking the structural intricacies of native tissue architecture, this approach enhances the biomimetic fidelity of engineered scaffolds, offering potential applications beyond kidney tissue engineering.
AB - A novel approach merging melt electrowriting (MEW) with matched die thermoforming to achieve scaffolds with micron-sized curvatures (200 – 800 µm versus 1000 µm of mandrel printing) for in vitro modeling of the kidney proximal tubule (PT) is proposed. Recent advances in this field emphasize the relevance of accurately replicating the intricate tissue microenvironment, particularly the curvature of the nephrons’ tubular segments. While MEW offers promising capabilities for fabricating highly and porous precise 3D structures mimicking the PT, challenges persist in approximating the diameter of tubular scaffolds to match the actual PT. The thermoformed MEW membranes retain the initial MEW printing design parameters (rhombus geometry, porosity > 45%) while accurately following the imprinted curvature (ratios between 0.67-0.95). PT epithelial cells cultured on these membranes demonstrate the ability to fill in the large pores of the membrane by secreting their own collagen IV-rich extracellular matrix and form an organized, functional, and tight monolayer expressing characteristic PT markers. Besides approximating PT architecture, this setup maximizes the usable surface area for cell culture and molecular readouts. By closely mimicking the structural intricacies of native tissue architecture, this approach enhances the biomimetic fidelity of engineered scaffolds, offering potential applications beyond kidney tissue engineering.
KW - curvature
KW - kidney tissue engineering
KW - melt electrowriting (MEW)
KW - proximal tubule (PT)
KW - thermoforming
KW - topography
UR - http://www.scopus.com/inward/record.url?scp=85208437744&partnerID=8YFLogxK
U2 - 10.1002/adhm.202401800
DO - 10.1002/adhm.202401800
M3 - Article
C2 - 39511873
AN - SCOPUS:85208437744
SN - 2192-2640
VL - 14
JO - Advanced healthcare materials
JF - Advanced healthcare materials
IS - 1
M1 - 2401800
ER -