Jevtić Predrag, Edens Lisa J, Li Xiaoyang, Nguyen Thang, Chen Pan, Levy Daniel L
From the Department of Molecular Biology, University of Wyoming, Laramie, Wyoming 82071.
From the Department of Molecular Biology, University of Wyoming, Laramie, Wyoming 82071
J Biol Chem. 2015 Nov 13;290(46):27557-71. doi: 10.1074/jbc.M115.673798. Epub 2015 Oct 1.
A fundamental question in cell biology concerns the regulation of organelle size. While nuclear size is exquisitely controlled in different cell types, inappropriate nuclear enlargement is used to diagnose and stage cancer. Clarifying the functional significance of nuclear size necessitates an understanding of the mechanisms and proteins that control nuclear size. One structural component implicated in the regulation of nuclear morphology is the nuclear lamina, a meshwork of intermediate lamin filaments that lines the inner nuclear membrane. However, there has not been a systematic investigation of how the level and type of lamin expression influences nuclear size, in part due to difficulties in precisely controlling lamin expression levels in vivo. In this study, we circumvent this limitation by studying nuclei in Xenopus laevis egg and embryo extracts, open biochemical systems that allow for precise manipulation of lamin levels by the addition of recombinant proteins. We find that nuclear growth and size are sensitive to the levels of nuclear lamins, with low and high concentrations increasing and decreasing nuclear size, respectively. Interestingly, each type of lamin that we tested (lamins B1, B2, B3, and A) similarly affected nuclear size whether added alone or in combination, suggesting that total lamin concentration, and not lamin type, is more critical to determining nuclear size. Furthermore, we show that altering lamin levels in vivo, both in Xenopus embryos and mammalian tissue culture cells, also impacts nuclear size. These results have implications for normal development and carcinogenesis where both nuclear size and lamin expression levels change.
细胞生物学中的一个基本问题涉及细胞器大小的调控。虽然在不同细胞类型中细胞核大小受到精确控制,但细胞核的异常增大被用于癌症的诊断和分期。阐明细胞核大小的功能意义需要了解控制细胞核大小的机制和蛋白质。一种与细胞核形态调控有关的结构成分是核纤层,它是内衬于内核膜的中间丝层粘连蛋白组成的网络。然而,尚未有关于层粘连蛋白表达水平和类型如何影响细胞核大小的系统性研究,部分原因是在体内精确控制层粘连蛋白表达水平存在困难。在本研究中,我们通过研究非洲爪蟾卵和胚胎提取物中的细胞核来规避这一限制,这些开放的生化系统允许通过添加重组蛋白精确操纵层粘连蛋白水平。我们发现细胞核的生长和大小对核纤层蛋白的水平敏感,低浓度和高浓度分别会增加和减小细胞核大小。有趣的是,我们测试的每种类型的层粘连蛋白(层粘连蛋白B1、B2、B3和A),无论单独添加还是组合添加,对细胞核大小的影响都相似,这表明决定细胞核大小的更关键因素是层粘连蛋白的总浓度,而非层粘连蛋白的类型。此外,我们表明,在非洲爪蟾胚胎和哺乳动物组织培养细胞中改变体内层粘连蛋白水平,也会影响细胞核大小。这些结果对正常发育和癌变具有启示意义,因为在这些过程中细胞核大小和层粘连蛋白表达水平都会发生变化。