Spatial and Temporal Scaling of Microtubules and Mitotic Spindles

• Published in: Cells (Basel, Switzerland) Vol. 11; no. 2; p. 248
• Main Authors: Lacroix, Benjamin, Dumont, Julien
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01-01-2022; MDPI
• Subjects: Adaptation; allometry; Animals; Cell cycle; Cell division; Cell Size; Cellular Biology; Chromosomes; embryonic development; Embryos; Humans; Life Sciences; Macromolecules; microtubule dynamics; Microtubules; Microtubules - metabolism; Mitosis; mitotic spindle; Models, Biological; Physiology; Review; Scaling; spatial scaling; Spindle Apparatus - metabolism; Spindles; Subcellular Processes; temporal scaling; Time Factors; allometry; spatial scaling; embryonic development; temporal scaling; microtubule dynamics; mitotic spindle
• ISSN: 2073-4409; 2073-4409
• DOI: 10.3390/cells11020248

During cell division, the mitotic spindle, a macromolecular structure primarily comprised of microtubules, drives chromosome alignment and partitioning between daughter cells. Mitotic spindles can sense cellular dimensions in order to adapt their length and mass to cell size. This scaling capacity is particularly remarkable during early embryo cleavage when cells divide rapidly in the absence of cell growth, thus leading to a reduction of cell volume at each division. Although mitotic spindle size scaling can occur over an order of magnitude in early embryos, in many species the duration of mitosis is relatively short, constant throughout early development and independent of cell size. Therefore, a key challenge for cells during embryo cleavage is not only to assemble a spindle of proper size, but also to do it in an appropriate time window which is compatible with embryo development. How spatial and temporal scaling of the mitotic spindle is achieved and coordinated with the duration of mitosis remains elusive. In this review, we will focus on the mechanisms that support mitotic spindle spatial and temporal scaling over a wide range of cell sizes and cellular contexts. We will present current models and propose alternative mechanisms allowing cells to spatially and temporally coordinate microtubule and mitotic spindle assembly.