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Hamid, Omar A; Eltaher, Hoda M; Sottile, Virginie; Yang, Jing
3D bioprinting of a stem cell-laden, multi-material tubular composite: An approach for spinal cord repair Journal Article
In: Mater. Sci. Eng. C Mater. Biol. Appl., vol. 120, no. 111707, pp. 111707, 2021.
Abstract | Tags: 3D printing, Embryoid body (EB), Gradient, Hydrogels, Nerve regeneration, Neural differentiation, Polycaprolactone
@article{Hamid2021-mr,
title = {3D bioprinting of a stem cell-laden, multi-material tubular
composite: An approach for spinal cord repair},
author = {Omar A Hamid and Hoda M Eltaher and Virginie Sottile and Jing Yang},
year = {2021},
date = {2021-01-01},
journal = {Mater. Sci. Eng. C Mater. Biol. Appl.},
volume = {120},
number = {111707},
pages = {111707},
publisher = {Elsevier BV},
abstract = {Development of a biomimetic tubular scaffold capable of
recreating developmental neurogenesis using pluripotent stem
cells offers a novel strategy for the repair of spinal cord
tissues. Recent advances in 3D printing technology have
facilitated biofabrication of complex biomimetic environments by
precisely controlling the 3D arrangement of various acellular
and cellular components (biomaterials, cells and growth
factors). Here, we present a 3D printing method to fabricate a
complex, patterned and embryoid body (EB)-laden tubular scaffold
composed of polycaprolactone (PCL) and hydrogel (alginate or
gelatine methacrylate (GelMA)). Our results revealed 3D printing
of a strong, macro-porous PCL/hydrogel tubular scaffold with a
high capacity to control the porosity of the PCL scaffold,
wherein the maximum porosity in the PCL wall was 15%. The
method was equally employed to create spatiotemporal protein
concentration within the scaffold, demonstrating its ability to
generate linear and opposite gradients of model molecules
(fluorescein isothiocyanate-conjugated bovine serum albumin
(FITC-BSA) and rhodamine). 3D bioprinting of EBs-laden GelMA was
introduced as a novel 3D printing strategy to incorporate EBs in
a hydrogel matrix. Cell viability and proliferation were
measured post-printing. Following the bioprinting of EBs-laden
5% GelMA hydrogel, neural differentiation of EBs was induced
using 1 μM retinoic acid (RA). The differentiated EBs
contained βIII-tubulin positive neurons displaying axonal
extensions and cells migration. Finally, 3D bioprinting of
EBs-laden PCL/GelMA tubular scaffold successfully supported EBs
neural differentiation and patterning in response to co-printing
with 1 μM RA. 3D printing of a complex heterogeneous tubular
scaffold that can encapsulate EBs, spatially controlled protein
concentration and promote neuronal patterning will help in
developing more biomimetic scaffolds capable of replicating the
neural patterning which occurs during neural tube development.},
keywords = {3D printing, Embryoid body (EB), Gradient, Hydrogels, Nerve regeneration, Neural differentiation, Polycaprolactone},
pubstate = {published},
tppubtype = {article}
}
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