TY - JOUR
T1 - A Cell Pre-Wrapping Seeding Technique for Hydrogel-Based Tubular Organ-On-A-Chip
AU - Nie, Jing
AU - Lou, Sha
AU - Pollet, Andreas M.A.O.
AU - van Vegchel, Manon
AU - Bouten, Carlijn V.C.
AU - den Toonder, Jaap M.J.
PY - 2024/8/14
Y1 - 2024/8/14
N2 - Organ-on-a-chip (OOC) models based on microfluidic technology are increasingly used to obtain mechanistic insight into (patho)physiological processes in humans, and they hold great promise for application in drug development and regenerative medicine. Despite significant progress in OOC development, several limitations of conventional microfluidic devices pose challenges. First, most microfluidic systems have rectangular cross sections and flat walls, and therefore tubular/ curved structures, like blood vessels and nephrons, are not well represented. Second, polymers used as base materials for microfluidic devices are much stiffer than in vivo extracellular matrix (ECM). Finally, in current cell seeding methods, challenges exist regarding precise control over cell seeding location, unreachable spaces due to flow resistances, and restricted dimensions/geometries. To address these limitations, an alternative cell seeding technique and a corresponding workflow is introduced to create circular cross-sectioned tubular OOC models by pre-wrapping cells around sacrificial fiber templates. As a proof of concept, a perfusable renal proximal tubule-on-a-chip is demonstrated with a diameter as small as 50 µm, cellular tubular structures with branches and curvature, and a preliminary vascular-renal tubule interaction model. The cell pre-wrapping seeding technique promises to enable the construction of diverse physiological/pathological models, providing tubular OOC systems for mechanistic investigations and drug development.
AB - Organ-on-a-chip (OOC) models based on microfluidic technology are increasingly used to obtain mechanistic insight into (patho)physiological processes in humans, and they hold great promise for application in drug development and regenerative medicine. Despite significant progress in OOC development, several limitations of conventional microfluidic devices pose challenges. First, most microfluidic systems have rectangular cross sections and flat walls, and therefore tubular/ curved structures, like blood vessels and nephrons, are not well represented. Second, polymers used as base materials for microfluidic devices are much stiffer than in vivo extracellular matrix (ECM). Finally, in current cell seeding methods, challenges exist regarding precise control over cell seeding location, unreachable spaces due to flow resistances, and restricted dimensions/geometries. To address these limitations, an alternative cell seeding technique and a corresponding workflow is introduced to create circular cross-sectioned tubular OOC models by pre-wrapping cells around sacrificial fiber templates. As a proof of concept, a perfusable renal proximal tubule-on-a-chip is demonstrated with a diameter as small as 50 µm, cellular tubular structures with branches and curvature, and a preliminary vascular-renal tubule interaction model. The cell pre-wrapping seeding technique promises to enable the construction of diverse physiological/pathological models, providing tubular OOC systems for mechanistic investigations and drug development.
KW - cell pre-wrapping seeding
KW - hydrogel
KW - renal proximal tubule
KW - sacrificial template
KW - tubular organ-on-a-chip
KW - Tissue Engineering/methods
KW - Humans
KW - Hydrogels/chemistry
KW - Rats
KW - Lab-On-A-Chip Devices
KW - Animals
KW - Microphysiological Systems
KW - Equipment Design/methods
UR - http://www.scopus.com/inward/record.url?scp=85195789026&partnerID=8YFLogxK
U2 - 10.1002/advs.202400970
DO - 10.1002/advs.202400970
M3 - Article
C2 - 38872259
AN - SCOPUS:85195789026
SN - 2198-3844
VL - 11
JO - Advanced Science
JF - Advanced Science
IS - 30
M1 - 2400970
ER -