Growth, homeostatic regulation and stem cell dynamics in tissues
The regulation of cell growth in animal tissues is a question of critical importance: most tissues contain different types of cells in interconversion and the fraction of each type has to be controlled in a precise way, by mechanisms that remain unclear. Here, we provide a theoretical framework for...
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Published in | Journal of the Royal Society interface Vol. 11; no. 93; p. 20130895 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
England
The Royal Society
06.04.2014
the Royal Society |
Subjects | |
Online Access | Get full text |
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Summary: | The regulation of cell growth in animal tissues is a question of critical importance: most tissues contain different types of cells in interconversion and the fraction of each type has to be controlled in a precise way, by mechanisms that remain unclear. Here, we provide a theoretical framework for the homeostasis of stem-cell-containing epithelial tissues using mechanical equations, which describe the size of the tissue and kinetic equations, which describe the interconversions of the cell populations. We show that several features, such as the evolution of stem cell fractions during intestinal development, the shape of a developing intestinal wall, as well as the increase in the proliferative compartment in cancer initiation, can be studied and understood from generic modelling which does not rely on a particular regulatory mechanism. Finally, inspired by recent experiments, we propose a model where cell division rates are regulated by the mechanical stresses in the epithelial sheet. We show that pressure-controlled growth can, in addition to the previous features, also explain with few parameters the formation of stem cell compartments as well as the morphologies observed when a colonic crypt becomes cancerous. We also discuss optimal strategies of wound healing, in connection with experiments on the cornea. |
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Bibliography: | ArticleID:rsif20130895 istex:C175580DE2D198FE272A0AD838F0BBB1473BFFDE href:rsif20130895.pdf ark:/67375/V84-4THVF50X-6 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 PMCID: PMC3928929 |
ISSN: | 1742-5689 1742-5662 |
DOI: | 10.1098/rsif.2013.0895 |