A computational model of nuclear self-organisation in syncytial embryos
Authored by Christoph Koke, Takuma Kanesaki, Joerg Grosshans, Ulrich S Schwarz, Carina M Dunlop
Date Published: 2014
DOI: 10.1016/j.jtbi.2014.06.001
Sponsors:
German Research Foundation (Deutsche Forschungsgemeinschaft, DFG)
Center for Modelling and Simulation in the Biosciences (BIOMS)
Platforms:
C++
Model Documentation:
Other Narrative
Mathematical description
Model Code URLs:
Model code not found
Abstract
Syncytial embryos develop through cycles of nuclear division and
rearrangement within a common cytoplasm. A paradigm example is
Drosophila melanogaster in which nuclei form an ordered array in the
embryo surface over cell cycles 10-13. This ordering process is assumed
to be essential for subsequent cellularisation. Using quantitative
tissue analysis, it has previously been shown that the regrowth of actin
and microtubule networks after nuclear division generates reordering
forces that counteract its disordering effect (Kanesaki et al., 2011).
We present here an individual-based computer simulation modelling the
nuclear dynamics. In contrast to similar modelling approaches e.g.
epithelial monolayers or tumour spheroids, we focus not on the spatial
dependence, but rather on the time-dependence of the interaction laws.
We show that appropriate phenomenological inter-nuclear force laws
reproduce the experimentally observed dynamics provided that the
cytoskeletal network regrows sufficiently quickly after mitosis. Then
repulsive forces provided by the actin system are necessary and
sufficient to regain the observed level of order in the system, after
the strong disruption resulting from cytoskeletal network disassembly
and spindle formation. We also observe little mixing of nuclei through
cell cycles. Our study highlights the importance of the dynamics of
cytoskeletal forces during this critical phase of syncytial development
and emphasises the need for real-time experimental data at high temporal
resolution. (C) 2014 Elsevier Ltd. All rights reserved.
Tags
Cell polarity
Cytoskeleton
Blastoderm
Crypt