Liu Zhonghua, Schatten Heide, Hao Yanhong, Lai Liangxue, Wax David, Samuel Melissa, Zhong Zhi-Sheng, Sun Qing-Yuan, Prather Randall S
Department of Animal Science, University of Missouri-Columbia, Columbia, MO 65211, USA.
Front Biosci. 2006 May 1;11:1945-57. doi: 10.2741/1937.
The Nuclear Mitotic Apparatus (NuMA) protein is a multifunctional protein that is localized to the nucleus in interphase and to the poles of the mitotic apparatus during mitosis. In unfertilized porcine oocytes, NuMA is localized to the meiotic spindle. NuMA is removed along with the meiotic spindle during the enucleation process before reconstructing the egg by introducing the donor cell nucleus to produce cloned embryos. Questions have been raised regarding the source for NuMA in cloned embryos, as the enucleated oocyte does not contain detectable NuMA in the cytoplasm. To determine the source of NuMA in porcine nuclear transfer (NT) embryos, we conducted an immunofluorescence microscopy study with antibodies against NuMA to investigate the appearance and distribution of NuMA before and after reconstructing NT embryos with porcine skin fibroblasts. We used donor cells from a confluent culture with all cells in interphase. For comparative studies, we also determined the immunofluorescence pattern of NuMA, gamma-tubulin, and alpha-tubulin in porcine fibroblasts, parthenogenetic embryos and in vitro fertilized (IVF) embryos. Results show that NuMA was localized in nuclei of 33.5% (163/456) of the serum-deprived fibroblasts used as donor cells. No NuMA staining was detected in enucleated pig oocytes. Immediately after nuclear transfer, NuMA staining was absent in all donor cell fibroblast nuclei (0 h) but staining was detected by 6 h within the reconstructed eggs, at which time the transferred somatic cell nucleus swelled in most cells (19/27) and became a pronucleus-like structure. NuMA was localized exclusively within the pronucleus-like structures (15/27). At 25 h, NuMA was detected inside the nucleus (16/25) either in one-cell or in 2-cell stage embryos. Interestingly, in parthenogenetic embryos, NuMA staining was not detected in all 42 eggs examined at 1 h, and evident NuMA staining was only detected inside a few (4/51 at 6 h; 6/48 at 25 h) of the nuclei. In IVF embryos, NuMA was detected within the nucleus at 6 h (5/20) and 25 h (13/16). These results show that the donor cell nucleus contains NuMA that is contributed to the reconstructed embryo and possibly activated by mechanisms in the oocyte's cytoplast.
核有丝分裂器(NuMA)蛋白是一种多功能蛋白,在间期定位于细胞核,在有丝分裂期间定位于有丝分裂器的两极。在未受精的猪卵母细胞中,NuMA定位于减数分裂纺锤体。在通过引入供体细胞核对卵子进行重构以产生克隆胚胎之前的去核过程中,NuMA会随着减数分裂纺锤体一起被去除。由于去核卵母细胞的细胞质中不含可检测到的NuMA,因此关于克隆胚胎中NuMA的来源引发了一些问题。为了确定猪核移植(NT)胚胎中NuMA的来源,我们使用抗NuMA抗体进行了免疫荧光显微镜研究,以调查在用猪皮肤成纤维细胞重构NT胚胎前后NuMA的出现和分布情况。我们使用来自汇合培养物且所有细胞都处于间期的供体细胞。为了进行比较研究,我们还确定了猪成纤维细胞、孤雌生殖胚胎和体外受精(IVF)胚胎中NuMA、γ-微管蛋白和α-微管蛋白的免疫荧光模式。结果显示,NuMA定位于用作供体细胞的33.5%(163/456)的血清饥饿成纤维细胞的细胞核中。在去核的猪卵母细胞中未检测到NuMA染色。核移植后立即,所有供体细胞成纤维细胞核(0小时)均未检测到NuMA染色,但在重构卵内6小时时检测到染色,此时大多数细胞(19/27)中转移的体细胞核肿胀并变成原核样结构。NuMA仅定位于原核样结构内(15/27)。在25小时时,在单细胞或二细胞期胚胎的细胞核内检测到NuMA(16/25)。有趣的是,在孤雌生殖胚胎中,在1小时检查的所有42个卵中均未检测到NuMA染色,仅在少数细胞核内(6小时时4/51;25小时时6/48)检测到明显的NuMA染色。在IVF胚胎中,在6小时(5/20)和25小时(13/16)时在细胞核内检测到NuMA。这些结果表明,供体细胞的细胞核含有NuMA,其被贡献给重构胚胎并可能由卵母细胞细胞质中的机制激活。