Generation and ex vivo characterization of a full-thickness substitute of the human urethra by tissue engineering
Metadatos
Mostrar el registro completo del ítemAutor
Sanchez-Porras, David; Etayo-Escanilla, Miguel; Moreno-Delgado, José-Andrés; Lozano-Martí, María del Mar; Bermejo-Casares, Fabiola; Alaminos-Mingorance, Miguel; Chato-Astrain, Jesús; Campos-Sánchez, Fernando; Sánchez-Quevedo, M. Carmen; Fernández-Valadés, RicardoEditorial
Wiley Periodicals LLC
Materia
Endothelium Fibrin-agarose biomaterial Human urethra
Fecha
2025-09-16Referencia bibliográfica
Sánchez-Porras D, Etayo-Escanilla M, Moreno-Delgado J-A, et al. Generation and ex vivo characterization of a full-thickness substitute of the human urethra by tissue engineering. Bioeng Transl Med. 2025;e70049. doi:10.1002/btm2.70049
Patrocinador
Spanish Ministry of Science and Innovation - Instituto de Salud Carlos III (Grant/Award Number: FIS PI22/00059); European Regional Development Fund (FEDER/ERDF)Resumen
Tissue engineering may offer efficient alternatives for the surgical repair of severe
conditions affecting the human urethra. However, development of tubular fullthickness substitutes is challenging. In this work, we have generated and evaluated
ex vivo a novel full-thickness human urethra substitute (FHUS) containing its three
main layers: the urethral mucosa (UM), the spongy layer (SP), and the tunica albuginea (AL). Results first showed that the generation of a FHUS significantly improved
the biomechanical properties of this artificial tissue as compared to the individual
layers, although the resistance of the native urethra was not reached. At the structural level, we found that FHUS shared important histological similarities with the
native urethra. Analysis of the individual layers showed that UM had a stratified epithelium that expressed several epithelial markers, including cytokeratins CK7 and
CK14, uroplakin 1b, and the intercellular junction proteins desmoplakin, tight junction
protein 1, and claudin. At the stromal level, UM tended to increase the presence of
collagen fibers and versican with time. The SP layer displayed abundant CD31 and
CD34-positive blood vessels, but small amounts of collagen and proteoglycans. The
AL layer showed scattered smooth muscle cells expressing α-smooth muscle actin,
smoothelin, and desmin cell markers, and contained low amounts of collagen and proteoglycans. Analysis of the basement membrane components collagen IV and laminin
revealed their progressive development with time, especially collagen IV. These
results confirm the possibility of developing a partially biomimetic full-thickness substitute of human urethra that might have potential clinical usefulness for the clinical
repair of severe urethral lesions.





