Histological Profiling of the Human Umbilical Cord: A Potential Alternative Cell Source in Tissue Engineering
Metadatos
Mostrar el registro completo del ítemAutor
Blanco Elices, Cristina; Chato Astrain, Jesús; Sánchez Porras, David; Carriel Araya, Víctor; Fernández Valadés, Ricardo; Sánchez Quevedo, María Del Carmen; Alaminos Mingorance, Miguel; Garzón Bello, Ingrid JohannaEditorial
MDPI
Materia
Umbilical cord MSC Vascular differentiation
Fecha
2022-04-18Referencia bibliográfica
Blanco-Elices, C... [et al.]. Histological Profiling of the Human Umbilical Cord: A Potential Alternative Cell Source in Tissue Engineering. J. Pers. Med. 2022, 12, 648. [https://doi.org/10.3390/jpm12040648]
Patrocinador
Spanish Plan Nacional de Investigacion Cientifica, Desarrollo e Innovacion Tecnologica (I+D+i) of the Spanish Ministry of Science and Innovation (Instituto de Salud Carlos III) FIS PI21/0980 FIS PI18/0331 FIS PI18/0332 FIS PI20/0317 FIS PI20/318 ICI19-00024; European Commission; Junta de Andalucia PE-0395-2019; University of Granada B-CTS-450-UGR20 CTS-498-UGR18; Consejeria de Transformacion Economica, Industria, Conocimiento y Universidades; Junta de Andalucia; European Commission Junta de Andalucia P18-RT-5059Resumen
The embryonic development of the human umbilical cord (hUC) is complex, and different
regions can be identified in this structure. The aim of this work is to characterize the hUC at in situ and
ex vivo levels to stablish their potential use in vascular regeneration. Human umbilical cords were
obtained and histologically prepared for in the situ analysis of four hUC regions (intervascular—IV,
perivascular—PV, subaminoblastic—SAM, and Wharton’s jelly—WH), and primary cell cultures of
mesenchymal stem cells (hUC-MSC) isolated from each region were obtained. The results confirmed
the heterogeneity of the hUC, with the IV and PV zones tending to show the higher in situ expression
of several components of the extracellular matrix (collagens, proteoglycans, and glycosaminoglycans),
vimentin, and MSC markers (especially CD73), although isolation and ex vivo culture resulted in a
homogeneous cell profile. Three vascular markers were positive in situ, especially vWF, followed
by CD34 and CD31, and isolation and culture revealed that the region associated with the highest
expression of vascular markers was IV, followed by PV. These results confirm the heterogeneity of
the hUC and the need for selecting cells from specific regions of the hUC for particular applications
in tissue engineering.