Please use this identifier to cite or link to this item:
https://doi.org/10.1371/journal.pcbi.1001045
DC Field | Value | |
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dc.title | A comprehensive model of the spatio-temporal stem cell and tissue organisation in the intestinal crypt | |
dc.contributor.author | Buske P. | |
dc.contributor.author | Galle J. | |
dc.contributor.author | Barker N. | |
dc.contributor.author | Aust G. | |
dc.contributor.author | Clevers H. | |
dc.contributor.author | Loeffler M. | |
dc.date.accessioned | 2019-11-06T09:32:36Z | |
dc.date.available | 2019-11-06T09:32:36Z | |
dc.date.issued | 2011 | |
dc.identifier.citation | Buske P., Galle J., Barker N., Aust G., Clevers H., Loeffler M. (2011). A comprehensive model of the spatio-temporal stem cell and tissue organisation in the intestinal crypt. PLoS Computational Biology 7 (1) : e1001045. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pcbi.1001045 | |
dc.identifier.issn | 1553734X | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/161656 | |
dc.description.abstract | We introduce a novel dynamic model of stem cell and tissue organisation in murine intestinal crypts. Integrating the molecular, cellular and tissue level of description, this model links a broad spectrum of experimental observations encompassing spatially confined cell proliferation, directed cell migration, multiple cell lineage decisions and clonal competition. Using computational simulations we demonstrate that the model is capable of quantitatively describing and predicting the dynamic behaviour of the intestinal tissue during steady state as well as after cell damage and following selective gain or loss of gene function manipulations affecting Wnt- and Notch-signalling. Our simulation results suggest that reversibility and flexibility of cellular decisions are key elements of robust tissue organisation of the intestine. We predict that the tissue should be able to fully recover after complete elimination of cellular subpopulations including subpopulations deemed to be functional stem cells. This challenges current views of tissue stem cell organisation. © 2011 Buske et al. | |
dc.rights | Attribution 4.0 International | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | Unpaywall 20191101 | |
dc.subject | beta catenin | |
dc.subject | Notch receptor | |
dc.subject | Wnt protein | |
dc.subject | Notch receptor | |
dc.subject | Wnt protein | |
dc.subject | analytic method | |
dc.subject | apoptosis | |
dc.subject | article | |
dc.subject | calculation | |
dc.subject | cell damage | |
dc.subject | cell interaction | |
dc.subject | cell lineage | |
dc.subject | cell migration | |
dc.subject | cell proliferation | |
dc.subject | cell subpopulation | |
dc.subject | controlled study | |
dc.subject | gene activity | |
dc.subject | gene expression | |
dc.subject | gene function | |
dc.subject | gene targeting | |
dc.subject | intestine crypt | |
dc.subject | mouse | |
dc.subject | nonhuman | |
dc.subject | prediction | |
dc.subject | simulation | |
dc.subject | stem cell | |
dc.subject | biological model | |
dc.subject | cytology | |
dc.subject | intestine | |
dc.subject | metabolism | |
dc.subject | signal transduction | |
dc.subject | Murinae | |
dc.subject | Apoptosis | |
dc.subject | Cell Proliferation | |
dc.subject | Intestines | |
dc.subject | Models, Biological | |
dc.subject | Receptors, Notch | |
dc.subject | Signal Transduction | |
dc.subject | Stem Cells | |
dc.subject | Wnt Proteins | |
dc.type | Article | |
dc.contributor.department | BIOCHEMISTRY | |
dc.description.doi | 10.1371/journal.pcbi.1001045 | |
dc.description.sourcetitle | PLoS Computational Biology | |
dc.description.volume | 7 | |
dc.description.issue | 1 | |
dc.description.page | e1001045 | |
Appears in Collections: | Elements Staff Publications |
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