Departamento de Física Atómica, Molecular y Nuclear and Departamento de Química Física I, Universidad Complutense, Avenida Complutense s/n, Madrid, Spain.
PLoS One. 2013 Aug 21;8(8):e69750. doi: 10.1371/journal.pone.0069750. eCollection 2013.
During symmetric division cells undergo large constriction deformations at a stable midcell site. Using a variational approach, we investigate the mechanical route for symmetric constriction by computing the bending energy of deformed vesicles with rotational symmetry. Forces required for constriction are explicitly computed at constant area and constant volume, and their values are found to be determined by cell size and bending modulus. For cell-sized vesicles, considering typical bending modulus of [Formula: see text], we calculate constriction forces in the range [Formula: see text]. The instability of symmetrical constriction is shown and quantified with a characteristic coefficient of the order of [Formula: see text], thus evidencing that cells need a robust mechanism to stabilize constriction at midcell.
在对称分裂过程中,细胞在稳定的细胞中部经历大的收缩变形。我们使用变分方法,通过计算具有旋转对称性的变形囊泡的弯曲能量,研究对称收缩的力学途径。在恒面积和恒体积的条件下,明确计算了收缩所需的力,并且发现它们的值由细胞大小和弯曲模量决定。对于细胞大小的囊泡,考虑到典型的弯曲模量[Formula: see text],我们计算出的收缩力范围为[Formula: see text]。显示并量化了对称收缩的不稳定性,其特征系数约为[Formula: see text],从而证明细胞需要一种稳健的机制来稳定细胞中部的收缩。