J Physiol. 2026 Jun 4. doi: 10.1113/JP290371. Online ahead of print.
ABSTRACT
Vascular smooth muscle cells (VSMCs) are the predominant cell type of the tunica media and are central mediators of vascular wall integrity, governing tone, remodelling and the progression of arterial disease. Despite this, mechanobiology research has historically focused on endothelial cells, leaving VSMC-intrinsic mechanosensing comparatively unexplored. Critically, VSMC phenotypic transitions from contractile to synthetic, inflammatory, osteogenic and macrophage-like states are not merely transcriptional events but involve profound bioenergetic reprogramming, a dimension that has been largely overlooked in mechanobiology. VSMCs sense and transduce diverse mechanical stimuli including cyclic stretch, shear stress, matrix stiffness and hydrostatic pressure through specialized mechanosensors such as mechanosensitive ion channels or cell surface receptors including integrins, to orchestrate phenotypic switching and vascular remodelling. Dysregulated mechanotransduction contributes to hypertension, atherosclerosis, aneurysm formation and arterial stiffening. This review provides a unified synthesis of VSMC mechanobiology across four domains: (1) mechanical microenvironment, (2) phenotypic plasticity, (3) mechanosensing pathways and (4) emerging technologies. In parallel the review also discusses emerging technologies such as organ-on-a-chip platforms that are increasingly being used to investigate these processes. Importantly, it introduces a novel integrated framework linking VSMC mechanotransduction, metabolic reprogramming and atherogenesis, positioning VSMCs at the centre of vascular mechanobiology and identifying the mechano-metabolic signalling as a therapeutically underexplored driver of cardiovascular disease.
PMID:42240569 | DOI:10.1113/JP290371