Cargando…

Modeling and Inferring Cleavage Patterns in Proliferating Epithelia

The regulation of cleavage plane orientation is one of the key mechanisms driving epithelial morphogenesis. Still, many aspects of the relationship between local cleavage patterns and tissue-level properties remain poorly understood. Here we develop a topological model that simulates the dynamics of...

Descripción completa

Detalles Bibliográficos
Autores principales: Patel, Ankit B., Gibson, William T., Gibson, Matthew C., Nagpal, Radhika
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2688032/
https://www.ncbi.nlm.nih.gov/pubmed/19521504
http://dx.doi.org/10.1371/journal.pcbi.1000412
_version_ 1782167642358939648
author Patel, Ankit B.
Gibson, William T.
Gibson, Matthew C.
Nagpal, Radhika
author_facet Patel, Ankit B.
Gibson, William T.
Gibson, Matthew C.
Nagpal, Radhika
author_sort Patel, Ankit B.
collection PubMed
description The regulation of cleavage plane orientation is one of the key mechanisms driving epithelial morphogenesis. Still, many aspects of the relationship between local cleavage patterns and tissue-level properties remain poorly understood. Here we develop a topological model that simulates the dynamics of a 2D proliferating epithelium from generation to generation, enabling the exploration of a wide variety of biologically plausible cleavage patterns. We investigate a spectrum of models that incorporate the spatial impact of neighboring cells and the temporal influence of parent cells on the choice of cleavage plane. Our findings show that cleavage patterns generate “signature” equilibrium distributions of polygonal cell shapes. These signatures enable the inference of local cleavage parameters such as neighbor impact, maternal influence, and division symmetry from global observations of the distribution of cell shape. Applying these insights to the proliferating epithelia of five diverse organisms, we find that strong division symmetry and moderate neighbor/maternal influence are required to reproduce the predominance of hexagonal cells and low variability in cell shape seen empirically. Furthermore, we present two distinct cleavage pattern models, one stochastic and one deterministic, that can reproduce the empirical distribution of cell shapes. Although the proliferating epithelia of the five diverse organisms show a highly conserved cell shape distribution, there are multiple plausible cleavage patterns that can generate this distribution, and experimental evidence suggests that indeed plants and fruitflies use distinct division mechanisms.
format Text
id pubmed-2688032
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-26880322009-06-12 Modeling and Inferring Cleavage Patterns in Proliferating Epithelia Patel, Ankit B. Gibson, William T. Gibson, Matthew C. Nagpal, Radhika PLoS Comput Biol Research Article The regulation of cleavage plane orientation is one of the key mechanisms driving epithelial morphogenesis. Still, many aspects of the relationship between local cleavage patterns and tissue-level properties remain poorly understood. Here we develop a topological model that simulates the dynamics of a 2D proliferating epithelium from generation to generation, enabling the exploration of a wide variety of biologically plausible cleavage patterns. We investigate a spectrum of models that incorporate the spatial impact of neighboring cells and the temporal influence of parent cells on the choice of cleavage plane. Our findings show that cleavage patterns generate “signature” equilibrium distributions of polygonal cell shapes. These signatures enable the inference of local cleavage parameters such as neighbor impact, maternal influence, and division symmetry from global observations of the distribution of cell shape. Applying these insights to the proliferating epithelia of five diverse organisms, we find that strong division symmetry and moderate neighbor/maternal influence are required to reproduce the predominance of hexagonal cells and low variability in cell shape seen empirically. Furthermore, we present two distinct cleavage pattern models, one stochastic and one deterministic, that can reproduce the empirical distribution of cell shapes. Although the proliferating epithelia of the five diverse organisms show a highly conserved cell shape distribution, there are multiple plausible cleavage patterns that can generate this distribution, and experimental evidence suggests that indeed plants and fruitflies use distinct division mechanisms. Public Library of Science 2009-06-12 /pmc/articles/PMC2688032/ /pubmed/19521504 http://dx.doi.org/10.1371/journal.pcbi.1000412 Text en Patel et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Patel, Ankit B.
Gibson, William T.
Gibson, Matthew C.
Nagpal, Radhika
Modeling and Inferring Cleavage Patterns in Proliferating Epithelia
title Modeling and Inferring Cleavage Patterns in Proliferating Epithelia
title_full Modeling and Inferring Cleavage Patterns in Proliferating Epithelia
title_fullStr Modeling and Inferring Cleavage Patterns in Proliferating Epithelia
title_full_unstemmed Modeling and Inferring Cleavage Patterns in Proliferating Epithelia
title_short Modeling and Inferring Cleavage Patterns in Proliferating Epithelia
title_sort modeling and inferring cleavage patterns in proliferating epithelia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2688032/
https://www.ncbi.nlm.nih.gov/pubmed/19521504
http://dx.doi.org/10.1371/journal.pcbi.1000412
work_keys_str_mv AT patelankitb modelingandinferringcleavagepatternsinproliferatingepithelia
AT gibsonwilliamt modelingandinferringcleavagepatternsinproliferatingepithelia
AT gibsonmatthewc modelingandinferringcleavagepatternsinproliferatingepithelia
AT nagpalradhika modelingandinferringcleavagepatternsinproliferatingepithelia