TY - JOUR
T1 - Microtubule-dependent transport and dynamics of vimentin intermediate filaments
AU - Hookway, Caroline
AU - Ding, Liya
AU - Davidson, Michael W.
AU - Rappoport, Joshua Z.
AU - Danuser, Gaudenz
AU - Gelfand, Vladimir I.
N1 - Publisher Copyright:
© 2015 Hookway et al.
PY - 2015/5/1
Y1 - 2015/5/1
N2 - We studied two aspects of vimentin intermediate filament dynamics - transport of filaments and subunit exchange. We observed transport of long filaments in the periphery of cells using live-cell structured illumination microscopy. We studied filament transport elsewhere in cells using a photoconvertible-vimentin probe and total internal reflection microscopy. We found that filaments were rapidly transported along linear tracks in both anterograde and retrograde directions. Filament transport was microtubule dependent but independent of microtubule polymerization and/or an interaction with the plus end-binding protein APC. We also studied subunit exchange in filaments by long-term imaging after photoconversion. We found that converted vimentin remained in small clusters along the length of filaments rather than redistributing uniformly throughout the network, even in cells that divided after photoconversion. These data show that vimentin filaments do not depolymerize into individual subunits; they recompose by severing and reannealing. Together these results show that vimentin filaments are very dynamic and that their transport is required for network maintenance.
AB - We studied two aspects of vimentin intermediate filament dynamics - transport of filaments and subunit exchange. We observed transport of long filaments in the periphery of cells using live-cell structured illumination microscopy. We studied filament transport elsewhere in cells using a photoconvertible-vimentin probe and total internal reflection microscopy. We found that filaments were rapidly transported along linear tracks in both anterograde and retrograde directions. Filament transport was microtubule dependent but independent of microtubule polymerization and/or an interaction with the plus end-binding protein APC. We also studied subunit exchange in filaments by long-term imaging after photoconversion. We found that converted vimentin remained in small clusters along the length of filaments rather than redistributing uniformly throughout the network, even in cells that divided after photoconversion. These data show that vimentin filaments do not depolymerize into individual subunits; they recompose by severing and reannealing. Together these results show that vimentin filaments are very dynamic and that their transport is required for network maintenance.
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U2 - 10.1091/mbc.E14-09-1398
DO - 10.1091/mbc.E14-09-1398
M3 - Article
C2 - 25717187
AN - SCOPUS:84929492895
SN - 1059-1524
VL - 26
SP - 1675
EP - 1686
JO - Molecular Biology of the Cell
JF - Molecular Biology of the Cell
IS - 9
ER -