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Effects of Donor Cell Types on the Development of Bovine Embryos Using Cytoplasm Injection Cloning Technology

Cytoplasm injection cloning technology (CICT) is an efficient technique for evaluating the developmental potential of cloned embryos. In this study, we investigated the effects of donor cell type on the developmental potential and quality of cloned bovine embryos. Adult fibroblasts (AFs) and embryon...

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Published in:International journal of molecular sciences 2021-05, Vol.22 (11), p.5841
Main Authors: Xu, Lianguang, Song, Seok-Hwan, Idrees, Muhammad, Mesalam, Ayman, Joo, Myeong-Don, Sidrat, Tabinda, Wei, Yiran, Lee, Kyeong-Lim, Lu, Wenfa, Kong, Il-Keun
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cited_by cdi_FETCH-LOGICAL-c427t-2659ad59954fd64efe3c9ab4fa97cd76e0920ecdaf73072e6396cfb3e7bf921c3
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container_issue 11
container_start_page 5841
container_title International journal of molecular sciences
container_volume 22
creator Xu, Lianguang
Song, Seok-Hwan
Idrees, Muhammad
Mesalam, Ayman
Joo, Myeong-Don
Sidrat, Tabinda
Wei, Yiran
Lee, Kyeong-Lim
Lu, Wenfa
Kong, Il-Keun
description Cytoplasm injection cloning technology (CICT) is an efficient technique for evaluating the developmental potential of cloned embryos. In this study, we investigated the effects of donor cell type on the developmental potential and quality of cloned bovine embryos. Adult fibroblasts (AFs) and embryonic cells (ECs) were used as donor cells to clone bovine embryos using CICT. We initially used AF cells to develop cloned embryos and then cultured the cloned day-8 blastocysts for 10 days to obtain ECs as donor cells for second embryo cloning. We found that the bovine blastocysts cloned using AF cells had significantly reduced developmental rates, embryo quality, and ratios of inner cell mass (ICM) to the total number of cells compared to those using ECs as donor cells. Furthermore, there were significant differences in the DNA methyltransferase-, histone deacetylation-, apoptosis-, and development-related genes at the blastocyst stage in embryos cloned from AFs compared to those in embryos cloned from ECs. Our results suggest that using ECs as donor cells for nuclear transfer enhances the quantity and quality of cloned embryos. However, further investigation is required in terms of determining pregnancy rates and developing cloned embryos from different donor cell types.
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