Abstract
The cytoskeleton plays a key role in establishing robust cell shape. In animals, it is well established that cell shape can also influence cytoskeletal organization. Cytoskeletal proteins are well conserved between animal and plant kingdoms; nevertheless, because plant cells exhibit major structural differences to animal cells, the question arises whether the plant cytoskeleton also responds to geometrical cues. Recent numerical simulations predicted that a geometry-based rule is sufficient to explain the microtubule (MT) organization observed in cells. Due to their high flexural rigidity and persistence length of the order of a few millimeters, MTs are rigid over cellular dimensions and are thus expected to align along their long axis if constrained in specific geometries. This hypothesis remains to be tested in cellulo Here, we explore the relative contribution of geometry to the final organization of actin and MT cytoskeletons in single plant cells of Arabidopsis thaliana We show that the cytoskeleton aligns with the long axis of the cells. We find that actin organization relies on MTs but not the opposite. We develop a model of self-organizing MTs in three dimensions, which predicts the importance of MT severing, which we confirm experimentally. This work is a first step toward assessing quantitatively how cellular geometry contributes to the control of cytoskeletal organization in living plant cells.
Highlights
The cytoskeleton plays a key role in establishing robust cell shape
We developed an experimental approach to explore the contribution of geometry to the final organization of actin and MT cytoskeletons in isolated plant cells lacking cell walls
To study how geometry affects cytoskeletal organization in plant cells, we developed a microwell-based approach allowing the control of the geometry of cells
Summary
The cytoskeleton plays a key role in establishing robust cell shape. In animals, it is well established that cell shape can influence cytoskeletal organization. Recent numerical simulations predicted that a geometry-based rule is sufficient to explain the microtubule (MT) organization observed in cells Due to their high flexural rigidity and persistence length of the order of a few millimeters, MTs are rigid over cellular dimensions and are expected to align along their long axis if constrained in specific geometries. Basic geometrical rules of the microtubules are computationally modeled in three dimensions and reveal the role of severing proteins in the shape response, which was observed experimentally. These findings demonstrate how cell geometry feeds back on cytoskeletal organization in plant cells
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