Arterial stiffness is a result of normal aging, and it is also a significant risk factor for heart failure. While the changes in the large scale mechanics of blood flow caused by arterial stiffness are well-studied, the perturbations of the microenvironment of the endothelial cell layer are not as well studied. The purpose of this research plan is to look at endothelial monolayers on different stiffness substrates in order to mimic the changes in the endothelial microenvironment during disease. This will be done by investigating the cytoskeleton of the cells - particularly the vimentin intermediate filament network as it has been shown to play a role in permeability of the monolayer. The cytoskeleton of single cells and confluent monolayers will be characterized by immunofluorescence and Western blotting - including a method that will characterize the ratio of the insoluble and soluble vimentin fractions. The stiffness of single endothelial cells and the endothelial monolayer will be quantified with atomic force microscopy measurements. Changes in cell stiffness will also be measured after perturbing different cytoskeletal elements with drugs. Finally, the permeability of endothelial cell monolayers will be studied on different stiffness substrates by a novel assay based on penetration of fluorescently labeled particles into the underlying hydrogel substrate. This proposal will help to further understand the affect of stiffening the arteries on the endothelial monolayer.

Public Health Relevance

As the body ages, the arteries become stiffer and this increased stiffness is a risk factor for cardiovascular disease. In this proposal, I will look at te changes in the endothelial cells (the cells that line the blood vessel) under both soft and stiff conditions in order to see if the change in the stiffness of the arteries causes changes in the function of the endothelial layer. This is important because it could help to explain why the stiffening in the arteries causes increased cardiovascular risk.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31AG041638-02
Application #
8366240
Study Section
Special Emphasis Panel (ZRG1-F10A-S (20))
Program Officer
Kohanski, Ronald A
Project Start
2011-09-30
Project End
2013-09-29
Budget Start
2012-09-30
Budget End
2013-09-29
Support Year
2
Fiscal Year
2012
Total Cost
$42,232
Indirect Cost
Name
University of Pennsylvania
Department
None
Type
Schools of Engineering
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Murray, Maria E; Mendez, Melissa G; Janmey, Paul A (2014) Substrate stiffness regulates solubility of cellular vimentin. Mol Biol Cell 25:87-94