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Cryopreservation and Laser Nanowarming of Zebrafish Embryos Followed by Hatching and Spawning
Author(s) -
Khosla Kanav,
Kangas Joseph,
Liu Yilin,
Zhan Li,
Daly Jonathan,
Hagedorn Mary,
Bischof John
Publication year - 2020
Publication title -
advanced biosystems
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.153
H-Index - 18
ISSN - 2366-7478
DOI - 10.1002/adbi.202000138
Subject(s) - hatching , cryopreservation , biology , embryo , zebrafish , perivitelline space , andrology , vitrification , yolk , aquaculture , human fertilization , fishery , embryogenesis , fish <actinopterygii> , zoology , anatomy , oocyte , zona pellucida , biochemistry , medicine , gene
This study shows for the first time the ability to rewarm cryopreserved zebrafish embryos that grow into adult fish capable of breeding normally. The protocol employs a single injection of cryoprotective agents (CPAs) and gold nanorods (GNRs) into the yolk and immersion in a precooling bath to dehydrate the perivitelline space. Then embryos are encapsulated within CPA and GNR droplets, plunged into liquid nitrogen, cryogenically stabilized, and rewarmed by a laser pulse. Postlaser nanowarming, embryos ( n  = 282) exhibit intact structure by 1 h (40%), continued development after 3 h (22%), movement after 24 h (11%), hatching after 48 h (9%), and swimming after Day 5 (3%). Finally, from fish that survives till Day 5, two larvae are grown to adulthood and spawned, yielding survival comparable to an unfrozen control. Future efforts will focus on improving the survival to adulthood and developing methods to cryopreserve large numbers of embryos for research, aquaculture, and biodiversity preservation.

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