Endothelial-to-mesenchymal transition contributes to fibro-proliferative vascular disease and is modulated by fluid shear stress. (17th June 2015)

• Record Type: Journal Article
• Authors: Moonen, Jan-Renier A.J.; Lee, Ee Soo; Schmidt, Marc; Maleszewska, Monika; Koerts, Jasper A.; Brouwer, Linda A.; van Kooten, Theo G.; van Luyn, Marja J.A.; Zeebregts, Clark J.; Krenning, Guido; Harmsen, Martin C.
• Is Part Of: Cardiovascular research. Volume 108:Number 3(2015)
• Page Start: 377
• Page End: 386
• Publication Date: 2015-06-17
• Subjects: Fibrosis -- Neointimal hyperplasia -- Endothelial-to-mesenchymal transition -- Shear stress -- ERK5; Cardiovascular system -- Diseases -- Periodicals; Cardiovascular system -- Periodicals; 616.1
• DOI: 10.1093/cvr/cvv175
• Languages: English
• ISSNs: 0008-6363

Abstract

Abstract: Aims: Neointimal hyperplasia is a common feature of fibro-proliferative vascular disease and characterizes initial stages of atherosclerosis. Neointimal lesions mainly comprise smooth muscle-like cells. The presence of these lesions is related to local differences in shear stress. Neointimal cells may arise through migration and proliferation of smooth muscle cells from the media. However, a role for the endothelium as a source of smooth muscle-like cells has largely been disregarded. Here, we investigated the role of endothelial-to-mesenchymal transition (EndMT) in neointimal hyperplasia and atherogenesis, and studied its modulation by shear stress. Methods and results: In human atherosclerotic plaques and porcine aortic tissues, myo-endothelial cells were identified, suggestive for EndMT. Flow disturbance by thoracic-aortic constriction in mice similarly showed the presence of myo-endothelial cells specifically in regions exposed to disturbed flow. While uniform laminar shear stress (LSS) was found to inhibit EndMT, endothelial cells exposed to disturbed flow underwent EndMT, in vitro and in vivo, and showed atherogenic differentiation. Gain- and loss-of-function studies using a constitutive active mutant of MEK5 and short hairpins targeting ERK5 established a pivotal role for ERK5 signalling in the inhibition of EndMT. Conclusion: Together, these data suggest that EndMT contributes to neointimal hyperplasia and induces atherogenic differentiation of endothelial cells. Importantly, we uncovered that EndMT is modulated by shear stress in an ERK5-dependent manner. These findings provide new insights in the role of adverse endothelial plasticity in vascular disease and identify a novel atheroprotective mechanism of uniform LSS, namely inhibition of EndMT.