Hayashi Masahito, Nishiyama Masayoshi, Kazayama Yuki, Toyota Taro, Harada Yoshie, Takiguchi Kingo
Division of Biological Science, Graduate School of Science, Nagoya University , Nagoya 464-8602, Japan.
Structural Biology Research Center, Nagoya University , Nagoya 464-8601, Japan.
Langmuir. 2016 Apr 19;32(15):3794-802. doi: 10.1021/acs.langmuir.6b00799. Epub 2016 Apr 6.
Liposomes encapsulating cytoskeletons have drawn much recent attention to develop an artificial cell-like chemical-machinery; however, as far as we know, there has been no report showing isothermally reversible morphological changes of liposomes containing cytoskeletons because the sets of various regulatory factors, that is, their interacting proteins, are required to control the state of every reaction system of cytoskeletons. Here we focused on hydrostatic pressure to control the polymerization state of microtubules (MTs) within cell-sized giant liposomes (diameters ∼10 μm). MT is the cytoskeleton formed by the polymerization of tubulin, and cytoskeletal systems consisting of MTs are very dynamic and play many important roles in living cells, such as the morphogenesis of nerve cells and formation of the spindle apparatus during mitosis. Using real-time imaging with a high-pressure microscope, we examined the effects of hydrostatic pressure on the morphology of tubulin-encapsulating giant liposomes. At ambient pressure (0.1 MPa), many liposomes formed protrusions due to tubulin polymerization within them. When high pressure (60 MPa) was applied, the protrusions shrank within several tens of seconds. This process was repeatedly inducible (around three times), and after the pressure was released, the protrusions regenerated within several minutes. These deformation rates of the liposomes are close to the velocities of migrating or shape-changing living cells rather than the shortening and elongation rates of the single MTs, which have been previously measured. These results demonstrate that the elongation and shortening of protrusions of giant liposomes is repeatedly controllable by regulating the polymerization state of MTs within them by applying and releasing hydrostatic pressure.
封装细胞骨架的脂质体最近备受关注,有望开发出一种类似人工细胞的化学机器;然而,据我们所知,尚未有报告显示含有细胞骨架的脂质体具有等温可逆的形态变化,因为需要各种调节因子(即它们的相互作用蛋白)来控制细胞骨架每个反应系统的状态。在这里,我们聚焦于静水压力来控制细胞大小的巨型脂质体(直径约10μm)内微管(MTs)的聚合状态。MT是由微管蛋白聚合形成的细胞骨架,由MTs组成的细胞骨架系统非常动态,在活细胞中发挥着许多重要作用,如神经细胞的形态发生和有丝分裂期间纺锤体的形成。使用高压显微镜进行实时成像,我们研究了静水压力对包裹微管蛋白的巨型脂质体形态的影响。在常压(0.1MPa)下,许多脂质体由于其内部微管蛋白的聚合而形成突起。当施加高压(60MPa)时,突起在几十秒内收缩。这个过程可以反复诱导(约三次),压力释放后,突起在几分钟内再生。脂质体的这些变形速率接近活细胞迁移或形状变化的速度,而不是先前测量的单个MTs的缩短和伸长速率。这些结果表明,通过施加和释放静水压力来调节巨型脂质体内MTs的聚合状态,可以反复控制其突起的伸长和缩短。