Long-Range Repulsion Between Chromosomes in Mammalian Oocyte Spindles

To prepare gametes with the appropriate number of chromosomes, mammalian oocytes undergo two sequential cell divisions. During each division, a large, long-lived, microtubule-based organelle called the meiotic spindle assembles around condensed chromosomes. Although meiotic spindles have been intensively studied for several decades, as force-generating mechanical objects, they remain very poorly understood. In materials physics, coarse-grained theories have been essential in understanding the large-scale behavior of systems composed of many interacting particles. It is unclear, however, if this approach can succeed in capturing the properties of active, biochemically complex, living materials like the spindle. Here, we show that a class of models based on nematic liquid crystal theory can describe important aspects of the organelle-scale structure and dynamics of spindles in living mouse oocytes. Using our models to interpret quantitative polarization microscopy data, we measure for the first time material properties relating to stress propagation in living oocytes, including the nematic diffusivities corresponding to splay and bend deformations. Unlike the reconstituted amphibian spindles that were previously studied in vitro, nematic elastic stress is exponentially screened in the microtubule network of living mammalian oocytes, with a screening length of order one micron. This observation can be explained by the relatively high volume fraction of embedded chromosomes in mammalian meiotic spindles, which cause long voids in the microtubule network and so disrupt orientational stress propagation.