| Literature DB >> 28481448 |
Jung Kyu Choi1, Rami El Assal1, Nicholas Ng2, Elizabeth Ginsburg2, Richard L Maas3, Raymond M Anchan2, Utkan Demirci1,4.
Abstract
The ability to cryopreserve human oocytes has significant potential for fertility preservation. Current cryopreservation methods still suffer from the use of conventional cryoprotectants, such as dimethyl sulphoxide (DMSO), causing loss of viability and function. Such injuries result from the toxicity and high concentration of cryoprotectants, as well as mechanical damage of cells due to ice crystal formation during the cooling and rewarming processes. Here we report the preservation of human oocytes following vitrification using an innovative bio-inspired cryoprotectant integrated with a minimum volume vitrification approach. The results demonstrate that the recovered human oocytes maintained viability following vitrification and rewarming. Moreover, when this approach was used to vitrify mouse oocytes, the recovered oocytes preserved their viability and function following vitrification and rewarming. This bio-inspired approach substitutes DMSO, a well-known toxic cryoprotectant, with ectoine, a non-toxic naturally occurring solute. The bio-inspired vitrification approach has the potential to improve fertility preservation for women undergoing cancer treatment and endangered mammal species.Entities:
Keywords: bio-inspired material; ectoine; human oocyte; low level of cryoprotectants; naturally inspired; vitrification
Mesh:
Year: 2017 PMID: 28481448 PMCID: PMC5766438 DOI: 10.1002/term.2439
Source DB: PubMed Journal: J Tissue Eng Regen Med ISSN: 1932-6254 Impact factor: 3.963