Effect of ECM and mechanical strain on vascular cell plasticity

Introduction: Depending on surrounding cell types, substrate mechanics, and chemical agonists, vascular smooth muscle cells (VSMCs) alternate between a contractile and synthetic phenotype. While endothelial cells (ECs) do not modulate their phenotype in this way, their behavior is highly dependent on location within the body. These variations are part of healthy vascular function, but improper phenotype has been implicated in cardiovascular disease. Atherosclerotic lesions, for example, have been found to be high in dedifferentiated, synthetic VSMCs as well as endothelial cells that have undergone endothelial to mesenchymal transition (EndMT). The overall goal of this project is to understand the effect of cross-talk between ECM and mechanical strain on vascular cell plasticity during aging. Materials and Methods: Mouse aortic smooth muscle cells (maSMCs) were isolated from C57Bl6 mice at less than 3 months (young), 6 to 10 months of age (middle-aged; MA), or greater than 15 months of age (old). Cells were then seeded onto dye-quenched (DQ) collagen type I (Col-I) substrate and measured for gain of fluorescent signal over 3 days. Human aortic endothelial cells (HAECs) were seeded onto glass cover slips or fibronectin coated PDMS chambers. Cells were further treated with or without TGF-β2 with daily media changes over 3 days. IF images were captured with a Leica Confocal microscope and quantification was performed using ImageJ. Results: ECs cultured on glass or treated with TGF-β2 show increased expression of SM22α and decreased expression of VECAD. Physiological strain (10%) did not cause changes in expression relative to static (0%). Mouse aortic SMCs isolated from older mice had significantly decreased rates of Col-I cleavage. Conclusions: maSMCs from older mice have lower Col-I turnover than their younger counterparts. This is consistent with bulk tissue behavior, as it is well known that relative collagen levels increase in the elastic vasculature as we age. HAECs on stiff substrates are more likely to show signs of EndMT – consistent with other studies. The addition of agonists such as TGF-β2 can reproduce this behavior in cells cultured on soft substrates. NASEM Ford Foundation Pre-Doctoral Fellowship and NHBLI grant R01HL148112 01 (L.S.) This is the full abstract presented at the American Physiology Summit 2023 meeting and is only available in HTML format. There are no additional versions or additional content available for this abstract. Physiology was not involved in the peer review process.

Duke Scholars

Author Sharon Gerecht Biomedical Engineering