Resumen de Cell viability evaluation of transdifferentiated endothelial-like cells by quantitative electronprobe X-ray microanalysis for tissue engineering

Manuel Vico, Alejandro Rodríguez Morata, Ingrid Garzón Bello, Fernando Campos Sánchez, B.D. Jaimes-Parra, Barbara Pérez-Köhle, María Julia Araceli Buján Varela, Miguel Alaminos Mingorance, María del Carmen Sánchez Quevedo

• Development of an efficient vascular substitute by tissue engineering is strongly dependent on endothelial cell viability. The aim of this study was to evaluate cell viability of transdifferentiated endotheliallike cells (Tr-ELC) by using for the first time electron probe X-ray microanalysis (EPXMA), not only to accurately analyze cell viability by quantifying the intracellular ionic concentrations, but also to establish their possible use in vascular tissue engineering protocols.

  Human umbilical cord Wharton�s jelly stem cells (HWJSC) and endothelial cells from the human umbilical vein (HUVEC) were isolated and cultured.

  Transdifferentiation from HWJSC to the endothelial phenotype was induced.

  EPXMA was carried out to analyze HUVEC, HWJSC and Tr-ELC cells by using a scanning electron microscope equipped with an EDAX DX-4 microanalytical system and a solid-state backscattered electron detector. To determine total ion content, the peak-to-local-background (P/B) ratio method was used with reference to standards composed of dextran containing known amounts of inorganic salts.

  Our results revealed a high K/Na ratio in Tr-ELC (9.41), in association with the maintenance of the intracellular levels of chlorine, phosphorous and magnesium and an increase of calcium (p=0.031) and sulfur (p=0.022) as compared to HWJSC. Calcium levels were similar for HUVEC and Tr-ELC. These results ensure that transdifferentiated cells are highly viable and resemble the phenotypic and microanalytical profile of endothelial cells.

  Tr-ELC induced from HWJSC may fulfill the requirements for use in tissue engineering protocols applied to the vascular system at the viability and microanalytical levels.