Biozentrum, University of Basel, Klingelbergstrasse 50-70, CH-4056 Basel, Switzerland.
Biozentrum, University of Basel, Klingelbergstrasse 50-70, CH-4056 Basel, Switzerland.
Curr Opin Cell Biol. 2014 Dec;31:84-91. doi: 10.1016/j.ceb.2014.09.005. Epub 2014 Sep 28.
Asymmetric cell division (ACD) is a mechanism to generate cellular diversity and used by prokaryotes and eukaryotes alike. Stem cells in particular rely on ACD to self-renew the stem cell while simultaneously generating a differentiating sibling. It is well established that the differential partitioning of cell fate determinants in the form of RNA and proteins between sibling cells induces changes in cell behavior and fate. Recently, insight into molecular mechanisms has been gained that could explain how centrosomes and centrosome-associated structures such as histones, chromosomes or the primary cilium, segregate asymmetrically. Similarly, many cell types also generate physical asymmetry in the form of sibling cell size differences. Emerging data suggests that spindle-induced cleavage furrow positioning through regulated spindle placement and spindle geometry is insufficient to explain all occurrence of cell-size asymmetry. Instead, asymmetric membrane extension based on asymmetric Myosin localization and cortical remodeling could be a driving force for the generation of physical asymmetry.
不对称细胞分裂(ACD)是一种产生细胞多样性的机制,原核生物和真核生物都有使用。干细胞特别依赖 ACD 来自我更新干细胞,同时产生一个分化的姊妹细胞。已经证实,以 RNA 和蛋白质形式存在的细胞命运决定因素在姊妹细胞之间的差异分配会引起细胞行为和命运的变化。最近,人们对分子机制有了深入的了解,这些机制可以解释中心体和中心体相关结构(如组蛋白、染色体或初级纤毛)如何不对称地分离。同样,许多细胞类型也以姊妹细胞大小差异的形式产生物理不对称性。新出现的数据表明,通过调节纺锤体位置和纺锤体几何形状来诱导分裂沟定位,不足以解释所有细胞大小不对称的发生。相反,基于不对称肌球蛋白定位和皮质重塑的不对称细胞膜延伸可能是产生物理不对称性的驱动力。
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