Evidence for Drop‐Like Nuclear Deformation in Sheared Endothelial Monolayers
Year: 2025
Type: article
Abstract: Shear stress imparted by blood flow tends to smoothen endothelial monolayers, a response classically attributed to reduced nuclear height and nuclear reorientation along flow. However, the mechanical basis remains unclear. Here, we tested predictions of the nuclear drop model-which posits that nuclear shape changes occur at constant volume and surface area-in human umbilical vein endothelial cells (HUVECs) under physiological shear stress. HUVEC nuclear morphologies varied from smooth, flat nuclei to wrinkled, tall ones. Applying shear stress reduced the frequency of tall, wrinkled nuclei, explaining the population-level decrease in nuclear height. Lamin A/C-depleted nuclei are highly irregular and failed to recover shapes postindentation on PDMS microposts, suggesting that lamin A/C confers nuclear surface tension. Nuclear volume and surface area remained constant under shear, consistent with the drop model, and a computational model based on these constraints successfully predicted observed nuclear shapes. Neither lamin A/C nor lamin B1 depletion prevented shear-induced YAP nuclear localization; instead, shear detached poorly spread cells, increasing spreading, focal adhesion assembly, and cytoskeletal tension in the remaining cells, thereby promoting YAP nuclear localization. These findings revise classical interpretations of flow-induced endothelial smoothing and show that flow-induced YAP nuclear localization results from increased cell spreading rather than nuclear deformation.
Source: Small
Authors: Mohammad Mohajeri, Ting‐Ching Wang, Pooja Agarwal, Simran Kaur, Ankit Kumar, Richard B. Dickinson, Abhishek Jain, Tanmay P. Lele
Language: English
Subfield: Cell Biology
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $5,790
Funders: National Science Foundation, National Aeronautics and Space Administration, Cancer Prevention and Research Institute of Texas, National Institutes of Health, U.S. Food and Drug Administration, Biomedical Advanced Research and Development Authority, National Heart, Lung, and Blood Institute, U.S. Army Medical Research Acquisition Activity
Awards: G3225075225, Collaborative Research: Biomechanics of Epithelial Tissue Homeostasis, Collapse, and Eversion, G3546748347, G392768340, G4756653596, Collaborative Research: Biomechanics of Epithelial Tissue Homeostasis, Collapse, and Eversion, G7658023295, Collaborative Research: Mechanics of the Topologically Complex Nuclear Envelope, Recruitment of Established Investigators, G9000112816
OpenAlex ID: W7117296861
