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首页> 外文期刊>Molecular reproduction and development >Proliferative characteristics and chromosomal stability of bovine donor cells for nuclear transfer.
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Proliferative characteristics and chromosomal stability of bovine donor cells for nuclear transfer.

机译:牛供体细胞核扩散的增殖特性和染色体稳定性。

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摘要

Few studies have characterized donor cell lines in terms of proliferative capacity and chromosomal stability. Abnormal phosphorylation patterns of the histones during metaphase could lead to abnormal chromosome segregation and extensive chromosome loss during mitosis. Suboptimal culture conditions may lead to abnormal histone H3 phosphorylation patterns, ultimately inducing missegregation and loss of chromosomes. The objective of the present study was to determine proliferative characteristics, chromosomal stability, and level of histone phosphorylation in cell lines established by explants and enzymatic dissociation. Proliferative characteristics, percentage of aneuploid cells, and relative levels of phosphorylated histone H3 (ser10) were determined at different population doublings (PD) by cell counting, karyotyping, and flow cytometry, respectively. The level of aneuploidies was high and remained elevated throughout the study independent of the technique used to establish the primary culture. Some cell lines had up to 50% of aneuploid cells during early passages. Multinucleated cells and abnormal spindle configurations were observed after prolonged time in culture (60 and 41%, respectively). An increase in the relative level of phosphorylated histone occurred after extended time in culture (55.7 during early passages vs. 102.6 at late passages). These data demonstrate the importance of determining chromosome content and the selection of healthy cell lines to decrease the percentage of aneuploid reconstructed embryos and increase the efficiency of nuclear transfer (NT).
机译:很少有研究以供体细胞系的增殖能力和染色体稳定性为特征。组蛋白在中期的异常磷酸化模式可能导致有丝分裂期间异常的染色体分离和广泛的染色体丢失。欠佳的培养条件可能会导致异常的组蛋白H3磷酸化模式,最终导致染色体的错误聚集和丢失。本研究的目的是确定外植体和酶解建立的细胞系的增殖特性,染色体稳定性和组蛋白磷酸化水平。通过细胞计数,核型分析和流式细胞术分别在不同的群体倍增率(PD)下确定增殖特征,非整倍体细胞百分比和磷酸化组蛋白H3(ser10)的相对水平。非整倍性水平很高,并且在整个研究过程中一直保持升高,而与用于建立原代培养的技术无关。在早期传代过程中,某些细胞系的非整倍体细胞高达50%。长时间培养后观察到多核细胞和纺锤体结构异常(分别为60%和41%)。延长培养时间后,磷酸化组蛋白的相对水平增加(早期传代时为55.7,晚期传代时为102.6)。这些数据证明了确定染色体含量和选择健康细胞系以降低非整倍体重建胚胎的百分比并提高核移植效率的重要性。

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