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猪粒细胞巨噬细胞集落刺激因子可改善克隆猪胚胎的体外发育。

Porcine granulocyte-macrophage colony-stimulating factor improves the in vitro development of cloned porcine embryos.

作者信息

Kwak Seong-Sung, Cheong Seung-A, Jeon Yubyeol, Hyun Sang-Hwan

机构信息

Laboratory of Veterinary Embryology and Biotechnology, College of Veterinary Medicine, Chungbuk National University, Cheongju 361-763, Republic of Korea.

出版信息

J Vet Med Sci. 2012 Sep;74(9):1095-102. doi: 10.1292/jvms.12-0050. Epub 2012 Apr 24.

Abstract

We examined the effects of porcine granulocyte-macrophage colony-stimulating factor (pGM-CSF) on the in vitro development of porcine embryos produced by somatic cell nuclear transfer (SCNT) for the first time. We evaluated the effects of pGM-CSF on SCNT-derived blastocyst formation and investigated gene expression. A total of 522 cloned embryos in 6 replicates were treated with 10 ng/ml pGM-CSF during in vitro culture (IVC). This treatment significantly (P<0.05) increased blastocyst formation and total cell number in blastocysts compared with the control (12.3% and 41.4 vs. 9.0% and 34.7, respectively). However, there was no effect on cleavage rate. The numbers of cells in the inner cell mass and trophectoderm were significantly higher in the pGM-CSF treatment group (6.0 and 43.0, respectively) compared with the control (4.4 and 31.9, respectively). Treatment with 10 ng/ml pGM-CSF significantly increased POU5F1 and Cdx2 mRNA expression in blastocysts. In addition, Bcl-2, Dnmt1 and proliferating cell nuclear antigen (PCNA) mRNA expression were upregulated in blastocysts in the pGM-CSF supplemented group compared with the control. These results suggest that pGM-CSF improves the quality and developmental viability of porcine SCNT embryos by regulating transcription factor expression.

摘要

我们首次研究了猪粒细胞巨噬细胞集落刺激因子(pGM-CSF)对体细胞核移植(SCNT)产生的猪胚胎体外发育的影响。我们评估了pGM-CSF对SCNT来源的囊胚形成的影响,并研究了基因表达。在体外培养(IVC)期间,对6个重复组中的总共522个克隆胚胎用10 ng/ml pGM-CSF进行处理。与对照组相比,这种处理显著(P<0.05)提高了囊胚形成率和囊胚中的总细胞数(分别为12.3%和41.4,而对照组分别为9.0%和34.7)。然而,对卵裂率没有影响。与对照组(分别为4.4和31.9)相比,pGM-CSF处理组的内细胞团和滋养外胚层中的细胞数显著更高(分别为6.0和43.0)。用10 ng/ml pGM-CSF处理显著增加了囊胚中POU5F1和Cdx2 mRNA的表达。此外,与对照组相比,补充pGM-CSF的组中囊胚的Bcl-2、Dnmt1和增殖细胞核抗原(PCNA)mRNA表达上调。这些结果表明,pGM-CSF通过调节转录因子表达来提高猪SCNT胚胎的质量和发育活力。

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