Article

Disturbed nuclear orientation and cellular migration in A-type lamin deficient cells.

Department of Molecular Cell Biology (Box 17), School for Cardiovascular Diseases (CARIM), Maastricht University, P.O. Box 616, NL-6200 MD Maastricht, The Netherlands.
Biochimica et Biophysica Acta (impact factor: 4.66). 11/2008; 1793(2):312-24. DOI:10.1016/j.bbamcr.2008.10.003 pp.312-24
Source: PubMed

ABSTRACT The nuclear lamina and the cytoskeleton form an integrated structure that warrants proper mechanical functioning of cells. We have studied the correlation between structural alterations and migrational behaviour in fibroblasts with and without A-type lamins. We show that loss of A-type lamins causes loss of emerin and nesprin-3 from the nuclear envelope, concurring with a disturbance in the connection between the nucleus and the cytoskeleton in A-type lamin-deficient (lmna -/-) cells. In these cells functional migration assays during in vitro wound healing revealed a delayed reorientation of the nucleus and the microtubule-organizing center during migration, as well as a loss of nuclear oscillatory rotation. These observations in fibroblasts isolated from lmna knockout mice were confirmed in a 3T3 cell line with stable reduction of lmna expression due to RNAi approach. Our results indicate that A-type lamins play a key role in maintaining directional movement governed by the cytoskeleton, and that the loss of these karyoskeletal proteins has important consequences for functioning of the cell as a mechanical entity.

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Keywords

3T3 cell line
 
A-type lamin-deficient
 
A-type lamins causes loss
 
cells functional migration assays
 
delayed reorientation
 
directional movement
 
integrated structure
 
karyoskeletal proteins
 
lmna -/-
 
lmna expression
 
lmna knockout mice
 
mechanical entity
 
microtubule-organizing center
 
migrational behaviour
 
nesprin-3
 
nuclear envelope
 
nuclear lamina
 
nuclear oscillatory rotation
 
stable reduction
 
warrants proper mechanical