» Articles » PMID: 34255994

Vascular Mechanobiology: Homeostasis, Adaptation, and Disease

Overview
Publisher Annual Reviews
Date 2021 Jul 13
PMID 34255994
Citations 68
Authors
Affiliations
Soon will be listed here.
Abstract

Cells of the vascular wall are exquisitely sensitive to changes in their mechanical environment. In healthy vessels, mechanical forces regulate signaling and gene expression to direct the remodeling needed for the vessel wall to maintain optimal function. Major diseases of arteries involve maladaptive remodeling with compromised or lost homeostatic mechanisms. Whereas homeostasis invokes negative feedback loops at multiple scales to mediate mechanobiological stability, disease progression often occurs via positive feedback that generates mechanobiological instabilities. In this review, we focus on the cell biology, wall mechanics, and regulatory pathways associated with arterial health and how changes in these processes lead to disease. We discuss how positive feedback loops arise via biomechanical and biochemical means. We conclude that inflammation plays a central role in overriding homeostatic pathways and suggest future directions for addressing therapeutic needs.

Citing Articles

In silico analyses of molecular force sensors for mechanical characterization of biological systems.

Lopez D, Castro C, Sotomayor M Biophys J. 2025; 124(5):829-843.

PMID: 39905731 PMC: 11897771. DOI: 10.1016/j.bpj.2025.01.025.


Biomechanics of soft biological tissues and organs, mechanobiology, homeostasis and modelling.

Holzapfel G, Humphrey J, Ogden R J R Soc Interface. 2025; 22(222):20240361.

PMID: 39876788 PMC: 11775666. DOI: 10.1098/rsif.2024.0361.


Pathophysiological Features of Remodeling in Vascular Diseases: Impact of Inhibitor of DNA-Binding/Differentiation-3 and Estrogenic Endocrine Disruptors.

Avecilla V, Doke M, Appunni S, Rubens M, Ramamoorthy V, Das J Med Sci (Basel). 2025; 13(1.

PMID: 39846697 PMC: 11755649. DOI: 10.3390/medsci13010002.


Endothelial cells under disturbed flow release extracellular vesicles to promote inflammatory polarization of macrophages and accelerate atherosclerosis.

Hou Z, Deng L, Fang F, Zhao T, Zhang Y, Li G BMC Biol. 2025; 23(1):20.

PMID: 39838385 PMC: 11753076. DOI: 10.1186/s12915-025-02125-x.


Mechanisms of aortic dissection: From pathological changes to experimental and models.

Rolf-Pissarczyk M, Schussnig R, Fries T, Fleischmann D, Elefteriades J, Humphrey J Prog Mater Sci. 2025; 150.

PMID: 39830801 PMC: 11737592. DOI: 10.1016/j.pmatsci.2024.101363.


References
1.
Parker M, Rossi D, Peterson M, Smith K, Sikstrom K, White E . Fibrotic extracellular matrix activates a profibrotic positive feedback loop. J Clin Invest. 2014; 124(4):1622-35. PMC: 3971953. DOI: 10.1172/JCI71386. View

2.
Xu J, Rodriguez D, Petitclerc E, Kim J, Hangai M, Moon Y . Proteolytic exposure of a cryptic site within collagen type IV is required for angiogenesis and tumor growth in vivo. J Cell Biol. 2001; 154(5):1069-79. PMC: 2196184. DOI: 10.1083/jcb.200103111. View

3.
Sakalihasan N, Limet R, Defawe O . Abdominal aortic aneurysm. Lancet. 2005; 365(9470):1577-89. DOI: 10.1016/S0140-6736(05)66459-8. View

4.
Saucerman J, Tan P, Buchholz K, McCulloch A, Omens J . Mechanical regulation of gene expression in cardiac myocytes and fibroblasts. Nat Rev Cardiol. 2019; 16(6):361-378. PMC: 6525041. DOI: 10.1038/s41569-019-0155-8. View

5.
Rajagopalan S, Meng X, Ramasamy S, Harrison D, Galis Z . Reactive oxygen species produced by macrophage-derived foam cells regulate the activity of vascular matrix metalloproteinases in vitro. Implications for atherosclerotic plaque stability. J Clin Invest. 1996; 98(11):2572-9. PMC: 507715. DOI: 10.1172/JCI119076. View