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PMID: 15367494 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Decreased mechanical stiffness in LMNA-/- cells is caused by defective nucleo-cytoskeletal integrity: implications for the development of laminopathies.

Human molecular genetics ·Vol. 13 ·No. 21 ·2004-11-01 ·Pages 2567-80

Broers JL, Peeters EA, Kuijpers HJ, Endert J, Bouten CV, Oomens CW, Baaijens FP, Ramaekers FC

Abstract

Laminopathies comprise a group of inherited diseases with variable clinical phenotypes, caused by mutations in the lamin A/C gene (LMNA). A prominent feature in several of these diseases is muscle wasting, as seen in Emery-Dreifuss muscle dystrophy, dilated cardiomyopathy and limb-girdle muscular dystrophy. Although the mechanisms underlying this phenotype remain largely obscure, two major working hypotheses are currently being investigated, namely, defects in gene regulation and/or abnormalities in nuclear architecture causing cellular fragility. In this study, using a newly developed cell compression device we have tested the latter hypothesis. The device allows controlled application of mechanical load onto single living cells, with simultaneous visualization of cellular deformation and quantitation of resistance. With the device, we have compared wild-type (MEF+/+) and LMNA knockout (MEF-/-) mouse embryonic fibroblasts (MEFs), and found that MEF-/- cells show a significantly decreased mechanical stiffness and a significantly lower bursting force. Partial rescue of the phenotype by transfection with either lamin A or lamin C prevented gross nuclear disruption, as seen in MEF-/- cells, but was unable to fully restore mechanical stiffness in these cells. Our studies show a direct correlation between absence of LMNA proteins and nuclear fragility in living cells. Simultaneous recordings by confocal microscopy revealed that the nuclei in MEF-/- cells, in contrast to MEF+/+ cells, exhibited an isotropic deformation upon indentation, despite an anisotropic deformation of the cell as a whole. This nuclear behaviour is indicative for a loss of interaction of the disturbed nucleus with the surrounding cytoskeleton. In addition, careful investigation of the three-dimensional organization of actin-, vimentin- and tubulin-based filaments showed a disturbed interaction of these structures in MEF-/- cells. Therefore, we suggest that in addition to the loss of nuclear stiffness, the loss of a physical interaction between nuclear structures (i.e. lamins) and the cytoskeleton is causing more general cellular weakness and emphasizes a potential key function for lamins in maintaining cellular tensegrity.

MeSH Terms
Actins/metabolism Animals Anisotropy Cell Nucleus/metabolism Cells, Cultured Cytoskeleton/metabolism Fibroblasts/metabolism,pathology Fluorescent Antibody Technique, Indirect Humans Lamin Type A/genetics,metabolism Lamins/genetics,metabolism Mice Mice, Knockout Microscopy, Confocal Mutation Stress, Mechanical Transfection Tubulin/metabolism Vimentin/metabolism
Chemicals
Actins Lamin Type A Lamins Tubulin Vimentin
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Broers Jos L V
Department of Moecular Cell Biology, Cardiovascular Research Institute Maastricht, University Maastricht, PO Box 616, NL-6200 MD Maastricht, The Netherlands. jos.broers@molcelb.unimaas.nl
Peeters Emiel A G
Kuijpers Helma J H
Endert Jorike
Bouten Carlijn V C
Oomens Cees W J
Baaijens Frank P T
Ramaekers Frans C S
Article Info
Journal
Human molecular genetics
Abbr.
Hum Mol Genet
ISSN
0964-6906
Published
2004-11-01
Epub
2004-00-14
Pages
2567-80
Language
English
Region
England
NLM ID
9208958
Subset
IM
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