TY - JOUR
T1 - A minimal actomyosin-based model predicts the dynamics of filopodia on neuronal dendrites
AU - Marchenko, Olena O.
AU - Das, Sulagna
AU - Yu, Ji
AU - Novak, Igor L.
AU - Rodionov, Vladimir I.
AU - Efimova, Nadia
AU - Svitkina, Tatyana
AU - Wolgemuth, Charles W.
AU - Loew, Leslie M.
N1 - Publisher Copyright:
© 2017 Taskin et al.
PY - 2017/4/15
Y1 - 2017/4/15
N2 - Dendritic filopodia are actin-filled dynamic subcellular structures that sprout on neuronal dendrites during neurogenesis. The exploratory motion of the filopodia is crucial for synaptogenesis, but the underlying mechanisms are poorly understood. To study filopodial motility, we collected and analyzed image data on filopodia in cultured rat hippocampal neurons. We hypothesized that mechanical feedback among the actin retrograde flow, myosin activity, and substrate adhesion gives rise to various filopodial behaviors. We formulated a minimal one-dimensional partial differential equation model that reproduced the range of observed motility. To validate our model, we systematically manipulated experimental correlates of parameters in the model: substrate adhesion strength, actin polymerization rate, myosin contractility, and the integrity of the putative microtubule-based barrier at the filopodium base. The model predicts the response of the system to each of these experimental perturbations, supporting the hypothesis that our actomyosin-driven mechanism controls dendritic filopodia dynamics.
AB - Dendritic filopodia are actin-filled dynamic subcellular structures that sprout on neuronal dendrites during neurogenesis. The exploratory motion of the filopodia is crucial for synaptogenesis, but the underlying mechanisms are poorly understood. To study filopodial motility, we collected and analyzed image data on filopodia in cultured rat hippocampal neurons. We hypothesized that mechanical feedback among the actin retrograde flow, myosin activity, and substrate adhesion gives rise to various filopodial behaviors. We formulated a minimal one-dimensional partial differential equation model that reproduced the range of observed motility. To validate our model, we systematically manipulated experimental correlates of parameters in the model: substrate adhesion strength, actin polymerization rate, myosin contractility, and the integrity of the putative microtubule-based barrier at the filopodium base. The model predicts the response of the system to each of these experimental perturbations, supporting the hypothesis that our actomyosin-driven mechanism controls dendritic filopodia dynamics.
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U2 - 10.1091/mbc.E16-06-0461
DO - 10.1091/mbc.E16-06-0461
M3 - Article
C2 - 28228546
AN - SCOPUS:85018528019
SN - 1059-1524
VL - 28
SP - 1021
EP - 1033
JO - Molecular biology of the cell
JF - Molecular biology of the cell
IS - 8
ER -