posted on 2023-03-23, 19:09authored byRosa F. Monteiro, Syeda M. Bakht, Manuel Gomez-Florit, Fernanda C. Stievani, Ana L. G. Alves, Rui L. Reis, Manuela E. Gomes, Rui M. A. Domingues
Tendinopathies are poorly understood diseases for which
treatment
remains challenging. Relevant in vitro models to
study human tendon physiology and pathophysiology are therefore highly
needed. Here we propose the automated 3D writing of tendon microphysiological
systems (MPSs) embedded in a biomimetic fibrillar support platform
based on cellulose nanocrystals (CNCs) self-assembly. Tendon decellularized
extracellular matrix (dECM) was used to formulate bioinks that closely
recapitulate the biochemical signature of tendon niche. A monoculture
system recreating the cellular patterns and phenotype of the tendon
core was first developed and characterized. This system was then incorporated
with a vascular compartment to study the crosstalk between the two
cell populations. The combined biophysical and biochemical cues of
the printed pattern and dECM hydrogel were revealed to be effective
in inducing human-adipose-derived stem cells (hASCs) differentiation
toward the tenogenic lineage. In the multicellular system, chemotactic
effects promoted endothelial cells migration toward the direction
of the tendon core compartment, while the established cellular crosstalk
boosted hASCs tenogenesis, emulating the tendon development stages.
Overall, the proposed concept is a promising strategy for the automated
fabrication of humanized organotypic tendon-on-chip models that will
be a valuable new tool for the study of tendon physiology and pathogenesis
mechanisms and for testing new tendinopathy treatments.