Vitamin C enhances in vitro and in vivo development of porcine somatic cell nuclear transfer embryos
► Report for the first time that vitamin C has a beneficial effect on the development of porcine SCNT embryos. ► The level of acH4K5 and Oct4 expression at blastocyst-stage was up-regulated after treatment. ► A higher rate of gestation and increased number of piglets born were harvested in the treat...
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Veröffentlicht in: | Biochemical and biophysical research communications 2011-07, Vol.411 (2), p.397-401 |
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Sprache: | eng |
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Zusammenfassung: | ► Report for the first time that vitamin C has a beneficial effect on the development of porcine SCNT embryos. ► The level of acH4K5 and Oct4 expression at blastocyst-stage was up-regulated after treatment. ► A higher rate of gestation and increased number of piglets born were harvested in the treated group.
The reprogramming of differentiated cells into a totipotent embryonic state through somatic cell nuclear transfer (SCNT) is still an inefficient process. Previous studies revealed that the generation of induced pluripotent stem (iPS) cells from mouse and human fibroblasts could be significantly enhanced with vitamin C treatment. Here, we investigated the effects of vitamin C, to our knowledge for the first time, on the in vitro and in vivo development of porcine SCNT embryos. The rate of blastocyst development in SCNT embryos treated with 50μg/mL vitamin C 15h after activation (36.0%) was significantly higher than that of untreated SCNT embryos (11.5%). The enhanced in vitro development rate of vitamin C-treated embryos was associated with an increased acetylation level of histone H4 lysine 5 and higher Oct4, Sox2 and Klf4 expression levels in blastocysts, as determined by real-time PCR. In addition, treatment with vitamin C resulted in an increased pregnancy rate in pigs. These findings suggest that treatment with vitamin C is beneficial for enhancement of the in vitro and in vivo development of porcine SCNT embryos. |
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ISSN: | 0006-291X 1090-2104 |
DOI: | 10.1016/j.bbrc.2011.06.160 |