Geometric model for dynamics of motor-driven centrosomal asters
The centrosomal aster is a mobile and adaptable cellular organelle that exerts and transmits forces necessary for tasks such as nuclear migration and spindle positioning. Recent experimental and theoretical studies of nematode and human cells demonstrate that pulling forces on asters by cortically a...
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| Format: | Article |
| Language: | English |
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American Physical Society
2025-01-01
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| Series: | Physical Review Research |
| Online Access: | http://doi.org/10.1103/PhysRevResearch.7.013004 |
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| author | Yuan-Nan Young Vicente Gomez Herrera Huan Zhang Reza Farhadifar Michael J. Shelley |
| author_facet | Yuan-Nan Young Vicente Gomez Herrera Huan Zhang Reza Farhadifar Michael J. Shelley |
| author_sort | Yuan-Nan Young |
| collection | DOAJ |
| description | The centrosomal aster is a mobile and adaptable cellular organelle that exerts and transmits forces necessary for tasks such as nuclear migration and spindle positioning. Recent experimental and theoretical studies of nematode and human cells demonstrate that pulling forces on asters by cortically anchored force generators are dominant during such processes. Here, we present a comprehensive investigation of the S-model (S for stoichiometry) of aster dynamics based solely on such forces. The model evolves the astral centrosome position, a probability field of cell-surface motor occupancy by centrosomal microtubules (under an assumption of stoichiometric binding), and free boundaries of unattached, growing microtubules. We show how cell shape affects the stability of centering of the aster, and its transition to oscillations with increasing motor number. Seeking to understand observations in single-cell nematode embryos, we use highly accurate simulations to examine the nonlinear structures of the bifurcations, and demonstrate the importance of binding domain overlap to interpreting genetic perturbation experiments. We find a generally rich dynamical landscape, dependent upon cell shape, such as internal constant-velocity equatorial orbits of asters that can be seen as traveling wave solutions. Finally, we study the interactions of multiple asters which we demonstrate an effective mutual repulsion due to their competition for surface force generators. We find, amazingly, that centrosomes can relax onto the vertices of platonic and nonplatonic solids, very closely mirroring the results of the classical Thomson problem for energy-minimizing configurations of electrons constrained to a sphere and interacting via repulsive Coulomb potentials. Our findings both explain experimental observations, providing insights into the mechanisms governing spindle positioning and cell division dynamics, and show the possibility of new nonlinear phenomena in cell biology. |
| format | Article |
| id | doaj-art-6d9afb7dbbac4a849275949dd8fafc19 |
| institution | Kabale University |
| issn | 2643-1564 |
| language | English |
| publishDate | 2025-01-01 |
| publisher | American Physical Society |
| record_format | Article |
| series | Physical Review Research |
| spelling | doaj-art-6d9afb7dbbac4a849275949dd8fafc192025-01-03T15:07:53ZengAmerican Physical SocietyPhysical Review Research2643-15642025-01-017101300410.1103/PhysRevResearch.7.013004Geometric model for dynamics of motor-driven centrosomal astersYuan-Nan YoungVicente Gomez HerreraHuan ZhangReza FarhadifarMichael J. ShelleyThe centrosomal aster is a mobile and adaptable cellular organelle that exerts and transmits forces necessary for tasks such as nuclear migration and spindle positioning. Recent experimental and theoretical studies of nematode and human cells demonstrate that pulling forces on asters by cortically anchored force generators are dominant during such processes. Here, we present a comprehensive investigation of the S-model (S for stoichiometry) of aster dynamics based solely on such forces. The model evolves the astral centrosome position, a probability field of cell-surface motor occupancy by centrosomal microtubules (under an assumption of stoichiometric binding), and free boundaries of unattached, growing microtubules. We show how cell shape affects the stability of centering of the aster, and its transition to oscillations with increasing motor number. Seeking to understand observations in single-cell nematode embryos, we use highly accurate simulations to examine the nonlinear structures of the bifurcations, and demonstrate the importance of binding domain overlap to interpreting genetic perturbation experiments. We find a generally rich dynamical landscape, dependent upon cell shape, such as internal constant-velocity equatorial orbits of asters that can be seen as traveling wave solutions. Finally, we study the interactions of multiple asters which we demonstrate an effective mutual repulsion due to their competition for surface force generators. We find, amazingly, that centrosomes can relax onto the vertices of platonic and nonplatonic solids, very closely mirroring the results of the classical Thomson problem for energy-minimizing configurations of electrons constrained to a sphere and interacting via repulsive Coulomb potentials. Our findings both explain experimental observations, providing insights into the mechanisms governing spindle positioning and cell division dynamics, and show the possibility of new nonlinear phenomena in cell biology.http://doi.org/10.1103/PhysRevResearch.7.013004 |
| spellingShingle | Yuan-Nan Young Vicente Gomez Herrera Huan Zhang Reza Farhadifar Michael J. Shelley Geometric model for dynamics of motor-driven centrosomal asters Physical Review Research |
| title | Geometric model for dynamics of motor-driven centrosomal asters |
| title_full | Geometric model for dynamics of motor-driven centrosomal asters |
| title_fullStr | Geometric model for dynamics of motor-driven centrosomal asters |
| title_full_unstemmed | Geometric model for dynamics of motor-driven centrosomal asters |
| title_short | Geometric model for dynamics of motor-driven centrosomal asters |
| title_sort | geometric model for dynamics of motor driven centrosomal asters |
| url | http://doi.org/10.1103/PhysRevResearch.7.013004 |
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