Abstract
Pluripotent human embryonic stem cells (hESCs) have an unlimited capacity for self-renewal and, in culture, to maintain their pluripotent capacity to differentiate into cell types from all three germ layers. Hundreds of stem cell lines have been derived worldwide from blastocysts of fresh and cryopreserved supernumerary embryos as well as from morula. Human embryonic stem cells hold tremendous promise as not only a tool for understanding disease, toxicology, and drug discovery but also as a basis for cell-based therapies for a wide range of human diseases including Parkinson’s and other neurodegenerative diseases, diabetes and gene, cardiac, and vascular therapy, and tissue engineering. The adoption of the vitrification method as the predominant cryopreservation method for hESCs is largely due to the definitive success of oocyte and embryo vitrification in the world. The vitrification protocols were very similar, all derived from the Kuwayama’s work developed for bovine ova and embryos and modified by Reubinoff for application to hESCs. Nowadays there are methods allowing an increase in the quantity of hESCs preserved at any one time, being big steps for a closer commercial scale-up. While the process is routine for hematopoietic stem cells and largely worked out for mesenchymal stem cells, at least for autologous use, now it is time to explore hESCs.
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Thanks to DVM Sergio Morado for his language assistance.
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Dalvit, G.C. (2015). Vitrification of Human Embryonic Stem Cells. In: Allahbadia, G., Kuwayama, M., Gandhi, G. (eds) Vitrification in Assisted Reproduction. Springer, New Delhi. https://doi.org/10.1007/978-81-322-1527-1_11
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DOI: https://doi.org/10.1007/978-81-322-1527-1_11
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