Abstract
Diseases caused by mutations in lamins A and C (laminopathies) suggest a crucial role for A-type lamins in different cellular processes. Laminopathies mostly affect tissues of mesenchymal origin. As transforming growth factor-β1 (TGF-β1) signalling impinges on the retinoblastoma protein (pRB) and SMADs, we tested the hypothesis that lamins modulate cellular responses to TGF-β1 signalling, via the regulation of these transcription factors in mesenchymal cells. Here, we report that A-type lamins are essential for the inhibition of fibroblast proliferation by TGF-β1. TGF-β1 dephosphorylated pRB through PP2A, both of which, we show, are associated with lamin A/C. In addition, lamin A/C modulates the effect of TGF-β1 on collagen production, a marker of mesenchymal differentiation. Our findings implicate lamin A/C in control of gene activity downstream of TGF-β1, via nuclear phosphatases such as PP2A. This biological function provides a novel explanation for the observed mesenchymal dysfunction in laminopathies. © The Author 2005. Published by Oxford University Press. All rights reserved.
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CITATION STYLE
Van Berlo, J. H., Voncken, J. W., Kubben, N., Broers, J. L. V., Duisters, R., van Leeuwen, R. E. W., … Pinto, Y. M. (2005). A-type lamins are essential for TGF-β1 induced PP2A to dephosphorylate transcription factors. Human Molecular Genetics, 14(19), 2839–2849. https://doi.org/10.1093/hmg/ddi316
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