Hiramoto Y, Hamaguchi Y, Shóji Y, Schroeder T E, Shimoda S, Nakamura S
J Cell Biol. 1981 Apr;89(1):121-30. doi: 10.1083/jcb.89.1.121.
Birefringence of the mitotic apparatus (MA) and its change during mitosis in sea urchin eggs were quantitatively determined using the birefringence detection apparatus reported in the preceding paper (Hiramoto el al., 1981, J. Cell Biol. 89:115-120). The birefringence and the form of the MA are represented by five parameters: peak retardation (delta p), through retardation (delta t), interpolar distance (D1), the distance (D2) between chromosome groups moving toward poles, and the distance (D3) between two retardation peaks. Distributions of birefringence retardation and the coefficient of birefringence in the spindle were quantitatively determined in MAs isolated during metaphase and anaphase. The distribution of microtubules (MTs) contained in the spindle is attributable to the form birefringence caused by regularly arranged MTs. The distribution coincided fairly well with the distribution of MTs in isolated MAs determined by electron microscopy. Under the same assumption, the distribution of MTS in the spindle in living cells during mitosis was determined. The results show that the distribution of MTs and the total amount of polymerized tubulin (MTs) in the spindle change during mitosis, suggesting the assembly and disassembly of MTs as well as the dislocation of MTs during mitosis.
利用前文(平本等人,1981年,《细胞生物学杂志》89卷:115 - 120页)报道的双折射检测装置,对海胆卵有丝分裂器(MA)的双折射及其在有丝分裂过程中的变化进行了定量测定。MA的双折射和形态由五个参数表示:峰值延迟(δp)、通透延迟(δt)、极间距离(D1)、向极移动的染色体组之间的距离(D2)以及两个延迟峰值之间的距离(D3)。在中期和后期分离得到的MA中,对纺锤体中双折射延迟和双折射系数的分布进行了定量测定。纺锤体中所含微管(MTs)的分布归因于由规则排列的MTs引起的形态双折射。该分布与通过电子显微镜测定的分离MA中MTs的分布相当吻合。在相同假设下,测定了有丝分裂期间活细胞纺锤体中MTs的分布。结果表明,有丝分裂期间纺锤体中MTs的分布和聚合微管蛋白(MTs)的总量发生变化,这表明有丝分裂期间MTs的组装和拆卸以及MTs的移位。