Senescent cultures of human dermal fibroblasts modified phenotype when immobilized in fibrin polymer

Cristian A. Acevedo, Donald I. Brown, Manuel E. Young, Juan G. Reyes

Resultado de la investigación: Contribución a una revistaArtículorevisión exhaustiva

10 Citas (Scopus)

Resumen

One of the limitations in tissue engineering is the restricted ability to expand the number of cells, because somatic cells can duplicate a limited number of times before they lose the ability to divide, leading to a senescent state. Here we report that the interaction of senescent fibroblasts with fibrin polymer can modify the senescent phenotype and partially restore the ability of growth-arrested cells to continue replicating. Primary human dermal fibroblasts were grown to >90% SA/β-Gal (senescence associated β-galactosidase) . The senescent cells were immobilized in fibrin-polymers by mixing fibrinogen and thrombin solutions. Immobilized senescent cell cultures grew, however, their growth arrested after 24 h of immobilization. The percentage of cells with a positive reaction at SA/β-Gal did not decrease significantly after immobilization, but the intensity of the stain decreased. The glycolytic activity in immobilized senescent fibroblast was re-established at pre-senescent levels. In conclusion, fibrin induces changes in the phenotype of senescent human fibroblasts. This simple procedure could complement available tissue-engineering techniques to increase the amount of biomass seeded on a fibrin scaffold, which could be beyond senescence.

Idioma originalInglés
Páginas (desde-hasta)1929-1942
Número de páginas14
PublicaciónJournal of Biomaterials Science, Polymer Edition
Volumen20
N.º13
DOI
EstadoPublicada - 1 sept. 2009
Publicado de forma externa

Huella

Profundice en los temas de investigación de 'Senescent cultures of human dermal fibroblasts modified phenotype when immobilized in fibrin polymer'. En conjunto forman una huella única.

Citar esto