4 research outputs found
Development of stromal differentiation patterns in heterotypical models of artificial corneas generated by tissue engineering
Supported Ministry of Science and Innovation (Instituto de Salud
Carlos III), grants FIS PI20/0317 and ICI21/00010 (NANOULCOR).
Supported by grant CSyF PI-0086-2020 from Consejería de Salud y
Familias, Junta de Andalucía, Spain and grant B-CTS-504-UGR20
(Programa Operativo FEDER Andalucía 2014-2020, University of
Granada and Consejería de Transformación Económica, Industria,
Conocimiento y Universidades). Cofinanced by the European
Regional Development Fund (ERDF) through the “Una manera de
hacer Europa” program.The Supplementary Material for this article can be found online
at: https://www.frontiersin.org/articles/10.3389/fbioe.2023.1124995/
full#supplementary-material
SUPPLEMENTARY FIGURE S1
Immunofluorescence analysis of the OAC and HAC tissues kept ex vivo and
grafted in vivo and control native human corneas (H) and rabbit corneas (R)
using an anti-human mitochondria primary antibody. Scale bar: 50 μm
(applicable to all images).Purpose: We carried out a histological characterization analysis of the stromal
layer of human heterotypic cornea substitutes generated with extra-corneal cells
to determine their putative usefulness in tissue engineering.
Methods: Human bioartificial corneas were generated using nanostructured
fibrin-agarose biomaterials with corneal stromal cells immersed within. To
generate heterotypical corneas, umbilical cord Wharton’s jelly stem cells
(HWJSC) were cultured on the surface of the stromal substitutes to obtain an
epithelial-like layer. These bioartificial corneas were compared with control native
human corneas and with orthotypical corneas generated with human corneal
epithelial cells on top of the stromal substitute. Both the corneal stroma and the
basement membrane were analyzed using histological, histochemical and
immunohistochemical methods in samples kept in culture and grafted in vivo
for 12 months in the rabbit cornea.
Results: Our results showed that the stroma of the bioartificial corneas kept ex vivo
showed very low levels of fibrillar and non-fibrillar components of the tissue
extracellular matrix. However, in vivo implantation resulted in a significant increase
of the contents of collagen, proteoglycans, decorin, keratocan and lumican in the
corneal stroma, showing higher levels of maturation and spatial organization of
these components. Heterotypical corneas grafted in vivo for 12 months showed
significantly higher contents of collagen fibers, proteoglycans and keratocan.
When the basement membrane was analyzed, we found that all corneas
grafted in vivo showed intense PAS signal and higher contents of nidogen-1,
although the levels found in human native corneas was not reached, and a
rudimentary basement membrane was observed using transmission electron
microscopy. At the epithelial level, HWJSC used to generate an epithelial-like
layer in ex vivo corneas were mostly negative for p63, whereas orthotypical
corneas and heterotypical corneas grafted in vivo were positive. Conclusion: These results support the possibility of generating bioengineered
artificial corneas using non-corneal HWJSC. Although heterotypical corneas
were not completely biomimetic to the native human corneas, especially ex
vivo, in vivo grafted corneas demonstrated to be highly biocompatible, and the
animal cornea became properly differentiated at the stroma and basement
membrane compartments. These findings open the door to the future clinical
use of these bioartificial corneas.Ministry of Science and Innovation (Instituto de Salud Carlos III)
FIS PI20/0317
ICI21/00010Junta de Andalucia
PI-0086-2020University of Granada and Consejeria de Transformacion Economica, Industria, Conocimiento y Universidades)
B-CTS-504-UGR20European Commissio
Electrochemical and In Situ Spectroscopic Evidences toward Empowering Ruthenium-Based Chalcogenides as Solid Acid Fuel Cell Cathodes
A low-cost Ru-based chalcogenide
catalyst has been used as a cathode
catalyst in solid acid fuel cells (SAFC). With sequential addition
of Se and Mo on Ru/C in a controlled manner, the resulting physical
and electrochemical properties have been discussed in detail. The
oxygen reduction reaction (ORR) in the presence of phosphoric acid
has been performed to appraise the tolerance of the catalyst in the
presence of phosphate anions. Considering the phosphate-rich environment
during cell operation, this study is especially relevant for designing
catalysts for s. In order to estimate the coverage of phosphate anions
on active sites, a semiquantitative analysis of the corresponding
Tafel plots has been done. Electrochemical, thermogravimetric, and
in situ X-ray absorption spectroscopic experiments have been performed
to get a deeper perception of the catalyst–electrolyte interface
and account for the high stability of the chalcogenide catalyst at
room temperature as well as at elevated temperature. Steady-state
polarization curves in SAFC have been collected for over 120 h using
the chalcogenide catalyst operating at 250 °C
Additional file 3: of Conceptions of learning factors in postgraduate health sciences master students: a comparative study with non-health science students and between genders
Table S3. Average ± standard deviation scores assigned to each item and to each factor for male and female students and p values of the statistical comparisons between genders for the students of each program using ANOVA (“P value” columns). Statistically significant p values are highlighted with asterisks (*). (PDF 375 kb
Additional file 1: of Conceptions of learning factors in postgraduate health sciences master students: a comparative study with non-health science students and between genders
Table S1. Factor number 7 related to “Learning as acquisition of professional competences” (PROF) added to the Conceptions of Learning Inventory (COLI) originally developed by Purdie and Hattie. (PDF 174 kb