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- W4387060954 abstract "One challenge that needs to be addressed in animal embryo production is to create the appropriate in vitro culture to improve the blastocyst rate and produce high-quality embryos. Buffalo Mesenchymal Stem Cells (MSCs) were derived from Wharton’s jelly and expanded in vitro. Conditioned media (secretome) was collected from well-characterized WJMSCs at 3rd passage. Similarly, buffalo Uterine Epithelial Cells (UECs) were derived from nongravid uteri and expanded in vitro. The secretome was collected from a well-characterized first passage UECs monolayer primed with steroid hormones (progesterone 3.14ng/ml and estradiol-17β 5 31pg/ml). Culture media was replaced with non-serum media, and the media was collected after 72h. Day 4 IVF-derived embryos were cultured in three groups: in regular mSOF media (Group I), mSOF replaced with 50% CM derived from MSCs (Group II), and mSOF replaced with 50% CM from steroid-treated UECs (Group III). Blastocyst rates were evaluated on day 09 post IVF. The blastocyst rate in group II was significantly higher (p < 0.05) than the control group, which was further enhanced in group III. In vitro co-culture of embryos with the secretome derived from mesenchymal stem cells or steroid-treated UECs improved the blastocyst rate. UECs and their secretions are essential to establish uterine receptivity and to mimic the internal in vivo environment." @default.
- W4387060954 created "2023-09-27" @default.
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- W4387060954 date "2023-09-12" @default.
- W4387060954 modified "2023-09-27" @default.
- W4387060954 title "Elucidating the Impact of Secretome Derived from Mesenchymal Stem Cell and Uterine Epithelial Cells During <i>In Vitro</i> Blastocyst Production in Buffalo" @default.
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- W4387060954 doi "https://doi.org/10.18311/jer/2023/34992" @default.
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