Geometric Effects in Large Scale Intracellular Flows

This work probes the role of cell geometry in orienting self-organized fluid flows in the late-stage oocyte. Recent theoretical work has shown that a model, which relies only on hydrodynamic interactions of flexible, cortically anchored microtubules and the mechanical loads from molecular motors moving upon them, is sufficient to generate observed flows. While the emergence of flows has been studied in spheres, oocytes change shape during streaming, and it was unclear how robust these flows are to the geometry of the cell. Here we use biophysical theory and computational analysis to investigate the role of geometry and find that the axis of rotation is set by the shape of the domain and that the flow is robust to biologically relevant perturbations of the domain shape. Using live imaging and three-dimensional flow reconstruction, we test the predictions of the theory/simulation, finding consistency between the model and live experiments, further demonstrating a geometric dependence on flow direction in late-stage oocytes.

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Publication Details

Journal
PRX Life
Published
2025-05-08
DOI
https://doi.org/10.1103/prxlife.3.023007
Primary Topic
Cellular Mechanics and Interactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Geometric Effects in Large Scale Intracellular Flows

Stanislav Y. Shvartsman, Reza Farhadifar, O. P. Jain, Elizabeth R. Gavis et al.
PRX Life
Cellular Mechanics and Interactions
article

Geometric Effects in Large Scale Intracellular Flows

Stanislav Y. Shvartsman, Reza Farhadifar, O. P. Jain, Elizabeth R. Gavis, Michael Shelley, Brato Chakrabarti
article en

Abstract

This work probes the role of cell geometry in orienting self-organized fluid flows in the late-stage oocyte. Recent theoretical work has shown that a model, which relies only on hydrodynamic interactions of flexible, cortically anchored microtubules and the mechanical loads from molecular motors moving upon them, is sufficient to generate observed flows. While the emergence of flows has been studied in spheres, oocytes change shape during streaming, and it was unclear how robust these flows are to the geometry of the cell. Here we use biophysical theory and computational analysis to investigate the role of geometry and find that the axis of rotation is set by the shape of the domain and that the flow is robust to biologically relevant perturbations of the domain shape. Using live imaging and three-dimensional flow reconstruction, we test the predictions of the theory/simulation, finding consistency between the model and live experiments, further demonstrating a geometric dependence on flow direction in late-stage oocytes.

PRX LifeVol. 3(2)
Princeton University (US), Courant Institute of Mathematical Sciences (US), Flatiron Health (United States) (US), Flatiron Institute (US)
National Science Foundation, Flatiron Health, Department of Atomic Energy, Government of India
Openalex Percentile: Top 90%
Cellular Mechanics and Interactions
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