TY - JOUR
T1 - Cellular Heterogeneity in Pressure and Growth Emerges from Tissue Topology and Geometry
AU - Long, Yuchen
AU - Cheddadi, Ibrahim
AU - Mosca, Gabriella
AU - Mirabet, Vincent
AU - Dumond, Mathilde
AU - Kiss, Annamaria
AU - Traas, Jan
AU - Godin, Christophe
AU - Boudaoud, Arezki
N1 - Publisher Copyright:
© 2020 Elsevier Inc.
PY - 2020/4/20
Y1 - 2020/4/20
N2 - Cell-to-cell heterogeneity prevails in many systems, as exemplified by cell growth, although the origin and function of such heterogeneity are often unclear. In plants, growth is physically controlled by cell wall mechanics and cell hydrostatic pressure, alias turgor pressure. Whereas cell wall heterogeneity has received extensive attention, the spatial variation of turgor pressure is often overlooked. Here, combining atomic force microscopy and a physical model of pressurized cells, we show that turgor pressure is heterogeneous in the Arabidopsis shoot apical meristem, a population of stem cells that generates all plant aerial organs. In contrast with cell wall mechanical properties that appear to vary stochastically between neighboring cells, turgor pressure anticorrelates with cell size and cell neighbor number (local topology), in agreement with the prediction by our model of tissue expansion, which couples cell wall mechanics and tissue hydraulics. Additionally, our model predicts two types of correlations between pressure and cellular growth rate, where high pressure may lead to faster- or slower-than-average growth, depending on cell wall extensibility, yield threshold, osmotic pressure, and hydraulic conductivity. The meristem exhibits one of these two regimes, depending on conditions, suggesting that, in this tissue, water conductivity may contribute to growth control. Our results unravel cell pressure as a source of patterned heterogeneity and illustrate links between local topology, cell mechanical state, and cell growth, with potential roles in tissue homeostasis.
AB - Cell-to-cell heterogeneity prevails in many systems, as exemplified by cell growth, although the origin and function of such heterogeneity are often unclear. In plants, growth is physically controlled by cell wall mechanics and cell hydrostatic pressure, alias turgor pressure. Whereas cell wall heterogeneity has received extensive attention, the spatial variation of turgor pressure is often overlooked. Here, combining atomic force microscopy and a physical model of pressurized cells, we show that turgor pressure is heterogeneous in the Arabidopsis shoot apical meristem, a population of stem cells that generates all plant aerial organs. In contrast with cell wall mechanical properties that appear to vary stochastically between neighboring cells, turgor pressure anticorrelates with cell size and cell neighbor number (local topology), in agreement with the prediction by our model of tissue expansion, which couples cell wall mechanics and tissue hydraulics. Additionally, our model predicts two types of correlations between pressure and cellular growth rate, where high pressure may lead to faster- or slower-than-average growth, depending on cell wall extensibility, yield threshold, osmotic pressure, and hydraulic conductivity. The meristem exhibits one of these two regimes, depending on conditions, suggesting that, in this tissue, water conductivity may contribute to growth control. Our results unravel cell pressure as a source of patterned heterogeneity and illustrate links between local topology, cell mechanical state, and cell growth, with potential roles in tissue homeostasis.
KW - atomic force microscopy
KW - biophysical modeling
KW - cellular heterogeneity
KW - growth mechanics
KW - hydrostatic pressure
KW - tissue hydraulics
KW - tissue topology
KW - turgor pressure
U2 - 10.1016/j.cub.2020.02.027
DO - 10.1016/j.cub.2020.02.027
M3 - Article
C2 - 32169211
AN - SCOPUS:85083304075
SN - 0960-9822
VL - 30
SP - 1504-1516.e8
JO - Current Biology
JF - Current Biology
IS - 8
ER -