Microtubule forces drive nuclear damage in LMNA cardiomyopathy

Nuclear homeostasis requires balanced forces between the cytoskeleton and the nucleus. Mutations in LMNA, which encodes lamin A/C, weaken the nuclear lamina, leading to nuclear damage and muscle disease. Disrupting the linker of nucleoskeleton and cytoskeleton (LINC) complex, which connects the cytoskeleton to the nucleus, may ameliorate LMNA-associated cardiomyopathy, yet the cardioprotective mechanism remains unclear. Here we developed an assay to quantify the coupling between cardiomyocyte contraction and nuclear deformation and interrogate its dependence on the nuclear lamina and LINC complex. The LINC complex was mostly dispensable for transferring contractile strain to the nucleus, and its disruption did not rescue elevated nuclear strain in lamin A/C-deficient cardiomyocytes. Instead, LINC complex disruption eliminated the microtubule cage encircling the nucleus. Microtubule disruption prevented nuclear damage and preserved cardiac function in lamin A/C deficiency. Computational modeling revealed that microtubule forces create local stress concentrations that damage lamin A/C-deficient nuclei. These findings identify microtubule-dependent force transmission as a pathological driver and therapeutic target for LMNA cardiomyopathy.

Authors

Institutions

Publication Details

Journal
Nature Cardiovascular Research
Published
2025-10-10
DOI
https://doi.org/10.1038/s44161-025-00727-w
Citations
1
Primary Topic
Nuclear Structure and Function
Type
article
Field-Weighted Citation Impact
0.81
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Microtubule forces drive nuclear damage in LMNA cardiomyopathy

Jan Lammerding, Vivek B. Shenoy, Rajan Jain, Benjamin L. Prosser et al.
1 citations
Nature Cardiovascular Research
Nuclear Structure and Function
0.81
article

Microtubule forces drive nuclear damage in LMNA cardiomyopathy

Jan Lammerding, Vivek B. Shenoy, Rajan Jain, Benjamin L. Prosser, Carmen Suay‐Corredera, Mohammad Dehghany, Daria Amiad Pavlov, Julie Heffler, Noam Zuela-Sopilniak, Keita Uchida, Rani Randell, Kaitlyn M Shen
article en
1 citations

Abstract

Nuclear homeostasis requires balanced forces between the cytoskeleton and the nucleus. Mutations in LMNA, which encodes lamin A/C, weaken the nuclear lamina, leading to nuclear damage and muscle disease. Disrupting the linker of nucleoskeleton and cytoskeleton (LINC) complex, which connects the cytoskeleton to the nucleus, may ameliorate LMNA-associated cardiomyopathy, yet the cardioprotective mechanism remains unclear. Here we developed an assay to quantify the coupling between cardiomyocyte contraction and nuclear deformation and interrogate its dependence on the nuclear lamina and LINC complex. The LINC complex was mostly dispensable for transferring contractile strain to the nucleus, and its disruption did not rescue elevated nuclear strain in lamin A/C-deficient cardiomyocytes. Instead, LINC complex disruption eliminated the microtubule cage encircling the nucleus. Microtubule disruption prevented nuclear damage and preserved cardiac function in lamin A/C deficiency. Computational modeling revealed that microtubule forces create local stress concentrations that damage lamin A/C-deficient nuclei. These findings identify microtubule-dependent force transmission as a pathological driver and therapeutic target for LMNA cardiomyopathy.

Nature Cardiovascular ResearchVol. 4(11)
Cornell University (US), Penn Center for AIDS Research (US), University of Pennsylvania (US)
Openalex Percentile: Top 23%
Nuclear Structure and Function
0.81
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.