NDA@SZTAKI

Vitrification of biopsied mouse embryos

Baranyai, B.

BodĂł, Sz.

Dinnyés, A.

GĂłcza, Elen

Akadémiai Kiadó

2005

info:eu-repo/date/embargoEnd/2025-01-31

SV Veterinary science / állatorvostudomány

Solid surface vitrification (SSV) was compared with in-straw vitrification for cryopreservation of biopsied mouse embryos. Eight-cell stage embryos were zona drilled and one blastomere was removed. Developed morulae or blastocysts were vitrified in microdrop (35% EG + 5% PVP + 0.4 M trehalose) or in straw (7.0 M EG + 0.5 M sucrose). Following recovery, embryos were cultivated in vi tro or transferred into recipients. Cryopreservation had an effect not only on the survival of biopsied embryos but also on their subsequent development in vitro. Cryosurvival of biopsied morulae vitrified in straw was significantly inferior to SSV. The post-warm development of biopsied and non-biopsied morulae was delayed on Day 3.5 and 4.5 in both vitrification groups. A delay in development was observed on Day 5.5 among vitrified non-biopsied blastocysts. The percentage of pups born from biopsied morulae or blastocysts following cryopreservation did not differ from that of the control. No significant differences could be detected between methods within and between embryonic stages in terms of birth rate. The birth rate of biopsied embryos vitrified in straw was significantly lower compared to the non-biopsied embryos. The novel cryopreservation protocol of SSV proved to be effective for cryopreservation of morula- and blastocyst-stage biopsied embryos.

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Article

PeerReviewed

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text

http://real.mtak.hu/48900/1/avet.53.2005.1.10.pdf

Baranyai, B. and Bodó, Sz. and Dinnyés, A. and Gócza, Elen (2005) Vitrification of biopsied mouse embryos. Acta Veterinaria Hungarica, 53 (1). pp. 103-112. ISSN 0236-6290

http://real.mtak.hu/48900/

http://dx.doi.org/10.1556/AVet.53.2005.1.10

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