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Development to term of sheep embryos reconstructed after inner cell mass/trophoblast exchange
P. Loi, C. Galli, G. Lazzari, K. Matsukawa, J. Fulka, F. Goeritz, TB. Hildebrandt,
Language English Country Japan
Document type Journal Article
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J-STAGE (Japan Science & Technology Information Aggregator, Electronic) Freely Available Titles - English
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from 1995
PubMed
29445070
DOI
10.1262/jrd.2017-109
Knihovny.cz E-resources
- MeSH
- Chimera embryology MeSH
- Ectogenesis * MeSH
- Blastocyst Inner Cell Mass cytology MeSH
- Fertilization in Vitro veterinary MeSH
- In Vitro Oocyte Maturation Techniques veterinary MeSH
- Abattoirs MeSH
- Cloning, Organism veterinary MeSH
- Microinjections veterinary MeSH
- Micromanipulation veterinary MeSH
- Animals, Newborn MeSH
- Sheep, Domestic MeSH
- Proof of Concept Study MeSH
- Embryo Transfer veterinary MeSH
- Cattle MeSH
- Feasibility Studies MeSH
- Pregnancy MeSH
- Trophoblasts cytology MeSH
- Fetal Development * MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Cattle MeSH
- Pregnancy MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Geographicals
- Italy MeSH
Here we report in vitro and term development of sheep embryos after the inner cell mass (ICM) from one set of sheep blastocysts were injected into the trophoblast vesicles of another set. We also observed successful in vitro development of chimeric blastocysts made from sheep trophoblast vesicles injected with bovine ICM. First, we dissected ICMs from 35 sheep blastocysts using a stainless steel microblade and injected them into 29 re-expanded sheep trophoblastic vesicles. Of the 25 successfully micromanipulated trophoblastic vesicles, 15 (51.7%) re-expanded normally and showed proper ICM integration. The seven most well reconstructed embryos were transferred for development to term. Three ewes receiving manipulated blastocysts were pregnant at day 45 (42.8%), and all delivered normal offspring (singletons, two females and one male, average weight: 3.54 ± 0.358 kg). Next, we monitored in vitro development of sheep trophoblasts injected with bovine ICMs. Of 17 injected trophoblastic vesicles, 10 (58.8%) re-expanded after 4 h in culture, and four (40%) exhibited integrated bovine ICM. Our results indicate that ICM/trophoblast exchange is feasible, allowing full term development with satisfactory lambing rate. Therefore, ICM exchange is a promising approach for endangered species conservation.
Avantea srl Laboratorio di Tecnologie della Riproduzione Cremona Italy
Institute of Animal Science Prague Czech Republic
Laboratory of Embryology Faculty of Veterinary Medicine University of Teramo 64100 Teramo Italy
Leibniz Institute for Zoo and Wildlife Research Berlin Germany
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