Theoretical tool bridging cell polarities with development of robust morphologies
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Theoretical tool bridging cell polarities with development of robust morphologies. / Nissen, Silas Boye; Rønhild, Steven; Trusina, Ala; Sneppen, Kim.
I: eLife, Bind 7, e38407, 27.11.2018.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Theoretical tool bridging cell polarities with development of robust morphologies
AU - Nissen, Silas Boye
AU - Rønhild, Steven
AU - Trusina, Ala
AU - Sneppen, Kim
PY - 2018/11/27
Y1 - 2018/11/27
N2 - Despite continual renewal and damages, a multicellular organism is able to maintain its complex morphology. How is this stability compatible with the complexity and diversity of living forms? Looking for answers at protein level may be limiting as diverging protein sequences can result in similar morphologies. Inspired by the progressive role of apical-basal and planar cell polarity in development, we propose that stability, complexity, and diversity are emergent properties in populations of proliferating polarized cells. We support our hypothesis by a theoretical approach, developed to effectively capture both types of polar cell adhesions. When applied to specific cases of development – gastrulation and the origins of folds and tubes – our theoretical tool suggests experimentally testable predictions pointing to the strength of polar adhesion, restricted directions of cell polarities, and the rate of cell proliferation to be major determinants of morphological diversity and stability.
AB - Despite continual renewal and damages, a multicellular organism is able to maintain its complex morphology. How is this stability compatible with the complexity and diversity of living forms? Looking for answers at protein level may be limiting as diverging protein sequences can result in similar morphologies. Inspired by the progressive role of apical-basal and planar cell polarity in development, we propose that stability, complexity, and diversity are emergent properties in populations of proliferating polarized cells. We support our hypothesis by a theoretical approach, developed to effectively capture both types of polar cell adhesions. When applied to specific cases of development – gastrulation and the origins of folds and tubes – our theoretical tool suggests experimentally testable predictions pointing to the strength of polar adhesion, restricted directions of cell polarities, and the rate of cell proliferation to be major determinants of morphological diversity and stability.
U2 - 10.7554/eLife.38407.001
DO - 10.7554/eLife.38407.001
M3 - Journal article
VL - 7
JO - eLife
JF - eLife
SN - 2050-084X
M1 - e38407
ER -
ID: 209799626