TY - JOUR
T1 - Renal proximal tubule-on-a-chip in PDMS
T2 - fabrication, functionalization, and RPTEC:HUVEC co-culture evaluation
AU - Guimaraes, Ana Paula Pereira
AU - Calori, Italo Rodrigo
AU - Stilhano, Roberta Sessa
AU - Tedesco, Antonio Claudio
N1 - Publisher Copyright:
© 2024 IOP Publishing Ltd.
PY - 2024/4/1
Y1 - 2024/4/1
N2 - ‘On-a-chip’ technology advances the development of physiologically relevant organ-mimicking architecture by integrating human cells into three-dimensional microfluidic devices. This method also establishes discrete functional units, faciliting focused research on specific organ components. In this study, we detail the development and assessment of a convoluted renal proximal tubule-on-a-chip (PT-on-a-chip). This platform involves co-culturing Renal Proximal Tubule Epithelial Cells (RPTEC) and Human Umbilical Vein Endothelial Cells (HUVEC) within a polydimethylsiloxane microfluidic device, crafted through a combination of 3D printing and molding techniques. Our PT-on-a-chip significantly reduced high glucose level, exhibited albumin uptake, and simulated tubulopathy induced by amphotericin B. Remarkably, the RPTEC:HUVEC co-culture exhibited efficient cell adhesion within 30 min on microchannels functionalized with plasma, 3-aminopropyltriethoxysilane, and type-I collagen. This approach significantly reduced the required incubation time for medium perfusion. In comparison, alternative methods such as plasma and plasma plus polyvinyl alcohol were only effective in promoting cell attachment to flat surfaces. The PT-on-a-chip holds great promise as a valuable tool for assessing the nephrotoxic potential of new drug candidates, enhancing our understanding of drug interactions with co-cultured renal cells, and reducing the need for animal experimentation, promoting the safe and ethical development of new pharmaceuticals.
AB - ‘On-a-chip’ technology advances the development of physiologically relevant organ-mimicking architecture by integrating human cells into three-dimensional microfluidic devices. This method also establishes discrete functional units, faciliting focused research on specific organ components. In this study, we detail the development and assessment of a convoluted renal proximal tubule-on-a-chip (PT-on-a-chip). This platform involves co-culturing Renal Proximal Tubule Epithelial Cells (RPTEC) and Human Umbilical Vein Endothelial Cells (HUVEC) within a polydimethylsiloxane microfluidic device, crafted through a combination of 3D printing and molding techniques. Our PT-on-a-chip significantly reduced high glucose level, exhibited albumin uptake, and simulated tubulopathy induced by amphotericin B. Remarkably, the RPTEC:HUVEC co-culture exhibited efficient cell adhesion within 30 min on microchannels functionalized with plasma, 3-aminopropyltriethoxysilane, and type-I collagen. This approach significantly reduced the required incubation time for medium perfusion. In comparison, alternative methods such as plasma and plasma plus polyvinyl alcohol were only effective in promoting cell attachment to flat surfaces. The PT-on-a-chip holds great promise as a valuable tool for assessing the nephrotoxic potential of new drug candidates, enhancing our understanding of drug interactions with co-cultured renal cells, and reducing the need for animal experimentation, promoting the safe and ethical development of new pharmaceuticals.
KW - 3D printing
KW - kidney
KW - organ-on-chip
KW - PDMS
KW - renal tubule
UR - http://www.scopus.com/inward/record.url?scp=85187203879&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85187203879&partnerID=8YFLogxK
U2 - 10.1088/1758-5090/ad2d2f
DO - 10.1088/1758-5090/ad2d2f
M3 - Article
C2 - 38408383
AN - SCOPUS:85187203879
SN - 1758-5082
VL - 16
JO - Biofabrication
JF - Biofabrication
IS - 2
M1 - 025024
ER -