Cargando…

Simulating Properties of In Vitro Epithelial Cell Morphogenesis

How do individual epithelial cells (ECs) organize into multicellular structures? ECs are studied in vitro to help answer that question. Characteristic growth features include stable cyst formation in embedded culture, inverted cyst formation in suspension culture, and lumen formation in overlay cult...

Descripción completa

Detalles Bibliográficos
Autores principales: Grant, Mark R, Mostov, Keith E, Tlsty, Thea D, Hunt, C. Anthony
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1592363/
https://www.ncbi.nlm.nih.gov/pubmed/17029556
http://dx.doi.org/10.1371/journal.pcbi.0020129
_version_ 1782130400047398912
author Grant, Mark R
Mostov, Keith E
Tlsty, Thea D
Hunt, C. Anthony
author_facet Grant, Mark R
Mostov, Keith E
Tlsty, Thea D
Hunt, C. Anthony
author_sort Grant, Mark R
collection PubMed
description How do individual epithelial cells (ECs) organize into multicellular structures? ECs are studied in vitro to help answer that question. Characteristic growth features include stable cyst formation in embedded culture, inverted cyst formation in suspension culture, and lumen formation in overlay culture. Formation of these characteristic structures is believed to be a consequence of an intrinsic program of differentiation and de-differentiation. To help discover how such a program may function, we developed an in silico analogue in which space, events, and time are discretized. Software agents and objects represent cells and components of the environment. “Cells” act independently. The “program” governing their behavior is embedded within each in the form of axioms and an inflexible decisional process. Relationships between the axioms and recognized cell functions are specified. Interactions between “cells” and environment components during simulation give rise to a complex in silico phenotype characterized by context-dependent structures that mimic counterparts observed in four different in vitro culture conditions: a targeted set of in vitro phenotypic attributes was matched by in silico attributes. However, for a particular growth condition, the analogue failed to exhibit behaviors characteristic of functionally polarized ECs. We solved this problem by following an iterative refinement method that improved the first analogue and led to a second: it exhibited characteristic differentiation and growth properties in all simulated growth conditions. It is the first model to simultaneously provide a representation of nonpolarized and structurally polarized cell types, and a mechanism for their interconversion. The second analogue also uses an inflexible axiomatic program. When specific axioms are relaxed, growths strikingly characteristic of cancerous and precancerous lesions are observed. In one case, the simulated cause is aberrant matrix production. Analogue design facilitates gaining deeper insight into such phenomena by making it easy to replace low-resolution components with increasingly detailed and realistic components.
format Text
id pubmed-1592363
institution National Center for Biotechnology Information
language English
publishDate 2006
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-15923632006-10-06 Simulating Properties of In Vitro Epithelial Cell Morphogenesis Grant, Mark R Mostov, Keith E Tlsty, Thea D Hunt, C. Anthony PLoS Comput Biol Research Article How do individual epithelial cells (ECs) organize into multicellular structures? ECs are studied in vitro to help answer that question. Characteristic growth features include stable cyst formation in embedded culture, inverted cyst formation in suspension culture, and lumen formation in overlay culture. Formation of these characteristic structures is believed to be a consequence of an intrinsic program of differentiation and de-differentiation. To help discover how such a program may function, we developed an in silico analogue in which space, events, and time are discretized. Software agents and objects represent cells and components of the environment. “Cells” act independently. The “program” governing their behavior is embedded within each in the form of axioms and an inflexible decisional process. Relationships between the axioms and recognized cell functions are specified. Interactions between “cells” and environment components during simulation give rise to a complex in silico phenotype characterized by context-dependent structures that mimic counterparts observed in four different in vitro culture conditions: a targeted set of in vitro phenotypic attributes was matched by in silico attributes. However, for a particular growth condition, the analogue failed to exhibit behaviors characteristic of functionally polarized ECs. We solved this problem by following an iterative refinement method that improved the first analogue and led to a second: it exhibited characteristic differentiation and growth properties in all simulated growth conditions. It is the first model to simultaneously provide a representation of nonpolarized and structurally polarized cell types, and a mechanism for their interconversion. The second analogue also uses an inflexible axiomatic program. When specific axioms are relaxed, growths strikingly characteristic of cancerous and precancerous lesions are observed. In one case, the simulated cause is aberrant matrix production. Analogue design facilitates gaining deeper insight into such phenomena by making it easy to replace low-resolution components with increasingly detailed and realistic components. Public Library of Science 2006-10 2006-10-06 /pmc/articles/PMC1592363/ /pubmed/17029556 http://dx.doi.org/10.1371/journal.pcbi.0020129 Text en © 2006 Grant 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
Grant, Mark R
Mostov, Keith E
Tlsty, Thea D
Hunt, C. Anthony
Simulating Properties of In Vitro Epithelial Cell Morphogenesis
title Simulating Properties of In Vitro Epithelial Cell Morphogenesis
title_full Simulating Properties of In Vitro Epithelial Cell Morphogenesis
title_fullStr Simulating Properties of In Vitro Epithelial Cell Morphogenesis
title_full_unstemmed Simulating Properties of In Vitro Epithelial Cell Morphogenesis
title_short Simulating Properties of In Vitro Epithelial Cell Morphogenesis
title_sort simulating properties of in vitro epithelial cell morphogenesis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1592363/
https://www.ncbi.nlm.nih.gov/pubmed/17029556
http://dx.doi.org/10.1371/journal.pcbi.0020129
work_keys_str_mv AT grantmarkr simulatingpropertiesofinvitroepithelialcellmorphogenesis
AT mostovkeithe simulatingpropertiesofinvitroepithelialcellmorphogenesis
AT tlstythead simulatingpropertiesofinvitroepithelialcellmorphogenesis
AT huntcanthony simulatingpropertiesofinvitroepithelialcellmorphogenesis