[HTML][HTML] Dysfunctional connections between the nucleus and the actin and microtubule networks in laminopathic models

CM Hale, AL Shrestha, SB Khatau… - Biophysical journal, 2008 - cell.com
CM Hale, AL Shrestha, SB Khatau, PJ Stewart-Hutchinson, L Hernandez, CL Stewart…
Biophysical journal, 2008cell.com
Laminopathies encompass a wide array of human diseases associated to scattered
mutations along LMNA, a single gene encoding A-type lamins. How such genetic alterations
translate to cellular defects and generate such diverse disease phenotypes remains
enigmatic. Recent work has identified nuclear envelope proteins—emerin and the linker of
the nucleoskeleton and cytoskeleton (LINC) complex—which connect the nuclear lamina to
the cytoskeleton. Here we quantitatively examine the composition of the nuclear envelope …
Abstract
Laminopathies encompass a wide array of human diseases associated to scattered mutations along LMNA, a single gene encoding A-type lamins. How such genetic alterations translate to cellular defects and generate such diverse disease phenotypes remains enigmatic. Recent work has identified nuclear envelope proteins—emerin and the linker of the nucleoskeleton and cytoskeleton (LINC) complex—which connect the nuclear lamina to the cytoskeleton. Here we quantitatively examine the composition of the nuclear envelope, as well as the architecture and functions of the cytoskeleton in cells derived from two laminopathic mouse models, including Hutchinson-Gilford progeria syndrome (LmnaL530P/L530P) and Emery-Dreifuss muscular dystrophy (Lmna−/−). Cells derived from the overtly aphenotypical model of X-linked Emery-Dreifuss muscular dystrophy (Emd−/y) were also included. We find that the centrosome is detached from the nucleus, preventing centrosome polarization in cells under flow—defects that are mediated by the loss of emerin from the nuclear envelope. Moreover, while basal actin and focal adhesion structure are mildly affected, RhoA activation, cell-substratum adhesion, and cytoplasmic elasticity are greatly lowered, exclusively in laminopathic models in which the LINC complex is disrupted. These results indicate a new function for emerin in cell polarization and suggest that laminopathies are not directly associated with cells' inability to polarize, but rather with cytoplasmic softening and weakened adhesion mediated by the disruption of the LINC complex across the nuclear envelope.
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