TY - JOUR
T1 - In silico leaf venation networks
T2 - Growth and reorganization driven by mechanical forces
AU - Corson, Francis
AU - Adda-Bedia, Mokhtar
AU - Boudaoud, Arezki
PY - 2009/8/7
Y1 - 2009/8/7
N2 - Development commonly involves an interplay between signaling, genetic expression and biophysical forces. However, the relative importance of these mechanisms during the different stages of development is unclear. Leaf venation networks provide a fitting context for the examination of these questions. In mature leaves, venation patterns are extremely diverse, yet their local structure satisfies a universal property: at junctions between veins, angles and diameters are related by a vectorial equation analogous to a force balance. Using a cell proliferation model, we reproduce in silico the salient features of venation patterns. Provided that vein cells are given different mechanical properties, tensile forces develop along the veins during growth, causing the network to deform progressively. Our results suggest that the local structure of venation networks results from a reorganization driven by mechanical forces, independently of how veins form. This conclusion is supported by recent observations of vein development in young leaves and by the good quantitative agreement between our simulations and data from mature leaves.
AB - Development commonly involves an interplay between signaling, genetic expression and biophysical forces. However, the relative importance of these mechanisms during the different stages of development is unclear. Leaf venation networks provide a fitting context for the examination of these questions. In mature leaves, venation patterns are extremely diverse, yet their local structure satisfies a universal property: at junctions between veins, angles and diameters are related by a vectorial equation analogous to a force balance. Using a cell proliferation model, we reproduce in silico the salient features of venation patterns. Provided that vein cells are given different mechanical properties, tensile forces develop along the veins during growth, causing the network to deform progressively. Our results suggest that the local structure of venation networks results from a reorganization driven by mechanical forces, independently of how veins form. This conclusion is supported by recent observations of vein development in young leaves and by the good quantitative agreement between our simulations and data from mature leaves.
KW - Mechanical stress
KW - Plant development
U2 - 10.1016/j.jtbi.2009.05.002
DO - 10.1016/j.jtbi.2009.05.002
M3 - Article
C2 - 19446571
AN - SCOPUS:67650144869
SN - 0022-5193
VL - 259
SP - 440
EP - 448
JO - Journal of Theoretical Biology
JF - Journal of Theoretical Biology
IS - 3
ER -