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Prelamin A causes aberrant myonuclear arrangement and results in muscle fiber weakness
Yotam Levy, … , Dawn A. Lowe, Julien Ochala
Yotam Levy, … , Dawn A. Lowe, Julien Ochala
Published October 4, 2018
Citation Information: JCI Insight. 2018;3(19):e120920. https://doi.org/10.1172/jci.insight.120920.
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Research Article Aging Muscle biology

Prelamin A causes aberrant myonuclear arrangement and results in muscle fiber weakness

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Abstract

Physiological and premature aging are frequently associated with an accumulation of prelamin A, a precursor of lamin A, in the nuclear envelope of various cell types. Here, we aimed to underpin the hitherto unknown mechanisms by which prelamin A alters myonuclear organization and muscle fiber function. By experimentally studying membrane-permeabilized myofibers from various transgenic mouse lines, our results indicate that, in the presence of prelamin A, the abundance of nuclei and myosin content is markedly reduced within muscle fibers. This leads to a concept by which the remaining myonuclei are very distant from each other and are pushed to function beyond their maximum cytoplasmic capacity, ultimately inducing muscle fiber weakness.

Authors

Yotam Levy, Jacob A. Ross, Marili Niglas, Vladimir A. Snetkov, Steven Lynham, Chen-Yu Liao, Megan J. Puckelwartz, Yueh-Mei Hsu, Elizabeth M. McNally, Manfred Alsheimer, Stephen D.R. Harridge, Stephen G. Young, Loren G. Fong, Yaiza Español, Carlos Lopez-Otin, Brian K. Kennedy, Dawn A. Lowe, Julien Ochala

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