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Updated: Jun 3, 2026

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Published on: June 26, 2015
Pericyte actomyosin-mediated contraction at the cell-material interface can modulate the microvascular niche
Sunyoung Lee1, Adam Zeiger, John M Maloney
1Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Pericytes use actin-mediated forces to buckle membranes, influencing microvasculature. This mechanical stimulation affects vascular endothelial cells, impacting angiogenesis in health and disease.
Area of Science:
- Cell biology
- Biophysics
- Vascular biology
Background:
- Pericytes are crucial cells surrounding capillaries, interacting with endothelial cells.
- These interactions influence microvasculature development and function.
- Pericytes possess contractile properties that can deform their environment.
Purpose of the Study:
- To investigate how pericyte contractile forces deform underlying membranes.
- To quantify the mechanical forces exerted by pericytes.
- To explore the impact of pericyte-induced mechanical changes on endothelial cells and angiogenesis.
Main Methods:
- Culturing pericytes on deformable silicone substrata.
- Imaging pericyte-generated wrinkles using optical and atomic force microscopy (AFM).
- Quantifying local stiffness and contractile forces using AFM nanoindentation and a mechanical model.
- Assessing the effects of cytoskeletal inhibitors on pericyte mechanics.
Main Results:
- Pericytes generated significant buckling contractions (average 38%) on the substrata via actin-mediated forces.
- Actomyosin forces were sufficient to deform the membrane.
- Pharmacological inhibition of the cytoskeleton altered contractile forces and local stiffness.
Conclusions:
- Pericyte contractile forces can deform the extracellular matrix in vitro.
- These mechanical deformations can act as a stimulus to adjacent vascular endothelial cells.
- Pericyte-induced mechanical changes may modulate cell-cell interactions, influencing angiogenesis in physiological and pathological contexts.
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