# Mechanical Regulation of Gene Expression in Ventricular Myocytes > **NIH NIH F31** · UNIVERSITY OF PENNSYLVANIA · 2021 · $12,152 ## Abstract Project Abstract Chronic changes in stress and strain on the heart are associated with the activation of gene programs that drive pathological growth and remodeling. Long-term upregulation of these genes can lead to cardiac hypertrophy and disease, yet how a change in mechanical force is transduced to a change in gene expression is poorly understood. Recent studies in non-muscle cells have found that strain transmission to the nucleus via the Linkers of the Nucleo- and Cytoskeleton (LINC) complex may be critical for force-dependent gene expression. The LINC complex forms protein-protein interactions that connect the cytoskeleton to the inner nuclear membrane and associated chromatin, forming a potential route for force-dependent gene regulation. Interestingly, mutations in many cytoskeletal, nucleoskeletal and LINC complex proteins have been linked to dilated cardiomyopathy (DCM). The experiments outlined in this proposal will define which components of the LINC complex and cytoskeleton transmit strain to the nucleus in adult cardiomyocytes (CMs), and whether those components are involved in strain-dependent gene expression. Based on my preliminary data, I hypothesize that the muscle- specific intermediate filament (IF) desmin and cardiac microtubules (MTs) are critical for strain transmission and regulate strain-dependent gene expression in adult CMs. The first goal of this proposal is to determine which LINC and cytoskeletal components transmit stress and strain to CM nuclei. I predict desmin and MTs will be critical for this process based on my preliminary evidence that depolymerization of the MT network reduces strain transmitted to nuclei. To determine which other components are important for strain transmission to the nucleus, I will assess the degree of nuclear deformation upon stretch/contraction in control myocytes and upon manipulations that disrupt desmin, actin, and components of the LINC complex. The second goal of this proposal is to determine whether the LINC complex and cytoskeleton contribute to strain- mediated gene expression. I hypothesize that desmin and MTs regulate strain-dependent gene expression via the LINC complex. I will test this hypothesis by cyclically stretching populations of isolated CMs and measuring alternations in gene expression using RNAseq both in control and in conditions where the cytoskeleton and LINC complex are disrupted. To complement this cellular approach, I will determine whether these components also regulate strain-dependent gene expression in an intact heart. These experiments will be the first to identify which components of the CM LINC complex and cytoskeleton regulate strain transmission to the nucleus and strain-induced gene expression. If successful, the results of this work will provide key insight into the mechanism by which chronic changes in stress and strain on the heart induce changes in gene expression. ## Key facts - **NIH application ID:** 10094235 - **Project number:** 5F31HL142238-03 - **Recipient organization:** UNIVERSITY OF PENNSYLVANIA - **Principal Investigator:** Julie Heffler - **Activity code:** F31 (R01, R21, SBIR, etc.) - **Funding institute:** NIH - **Fiscal year:** 2021 - **Award amount:** $12,152 - **Award type:** 5 - **Project period:** 2019-01-01 → 2021-05-17 ## Primary source NIH RePORTER: https://reporter.nih.gov/project-details/10094235 ## Citation > US National Institutes of Health, RePORTER application 10094235, Mechanical Regulation of Gene Expression in Ventricular Myocytes (5F31HL142238-03). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/10094235. Licensed CC0. --- *[NIH grants dataset](/datasets/nih-grants) · CC0 1.0*