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<title>Biocasting of an elastin-like recombinamer and collagen bi-layered model of the tunica adventitia and external elastic lamina of the vascular wall</title>
<creator>González Pérez, Miguel</creator>
<creator>Camasão, Dimitria Bonizol</creator>
<creator>Mantovani, Diego</creator>
<creator>Alonso Rodrigo, Matilde</creator>
<creator>Rodríguez Cabello, José Carlos</creator>
<description>Producción Científica</description>
<description>The development of techniques for fabricating vascular wall models will foster the development of preventive&#xd;
and therapeutic therapies for treating cardiovascular diseases. However, the physical and biological&#xd;
complexity of vascular tissue represents a major challenge, especially for the design and the production&#xd;
of off-the-shelf biomimetic vascular replicas. Herein, we report the development of a biocasting&#xd;
technique that can be used to replicate the tunica adventitia and the external elastic lamina of the vascular&#xd;
wall. Type I collagen embedded with neonatal human dermal fibroblast (HDFn) and an elastic click crosslinkable,&#xd;
cell-adhesive and protease-sensitive elastin-like recombinamer (ELR) hydrogel were investigated&#xd;
as readily accessible and tunable layers to the envisaged model. Mechanical characterization confirmed&#xd;
that the viscous and elastic attributes predominated in the collagen and ELR layers, respectively. In vitro&#xd;
maturation confirmed that the collagen and ELR provided a favorable environment for the HDFn viability,&#xd;
while histology revealed the wavy and homogenous morphology of the ELR and collagen layer respectively,&#xd;
the cell polarization towards the cell-attachment sites encoded on the ELR, and the enhanced&#xd;
expression of glycosaminoglycan-rich extracellular matrix and differentiation of the embedded HDFn into&#xd;
myofibroblasts. As a complementary assay, 30% by weight of the collagen layer was substituted with the&#xd;
ELR. This model proved the possibility to tune the composition and confirm the versatile character of the&#xd;
technology developed, while revealing no significant differences with respect to the original construct.&#xd;
On-demand modification of the model dimensions, number and composition of the layers, as well as the&#xd;
type and density of the seeded cells, can be further envisioned, thus suggesting that this bi-layered model&#xd;
may be a promising platform for the fabrication of biomimetic vascular wall models.</description>
<date>2021-08-12</date>
<date>2021-08-12</date>
<date>2021</date>
<type>info:eu-repo/semantics/article</type>
<identifier>Biomater. Sci., 2021, 9, 3860–3874</identifier>
<identifier>2047-4830</identifier>
<identifier>https://uvadoc.uva.es/handle/10324/47857</identifier>
<identifier>10.1039/d0bm02197k</identifier>
<identifier>3860</identifier>
<identifier>10</identifier>
<identifier>3874</identifier>
<identifier>Biomaterials Science</identifier>
<identifier>9</identifier>
<identifier>2047-4849</identifier>
<language>spa</language>
<relation>http//:rsc.li/biomaterials-science</relation>
<rights>info:eu-repo/semantics/openAccess</rights>
<publisher>The Royal Society of Chemistry</publisher>
</thesis></metadata></record></GetRecord></OAI-PMH>