Human haemodynamic frequency harmonics regulate the inflammatory phenotype of vascular endothelial cells

Haemodynamic variations are inherent to blood vessel geometries (such as bifurcations) and correlate with regional development of inflammation and atherosclerosis. However, the complex frequency spectrum characteristics from these haemodynamics have never been exploited to test whether frequency var...

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Veröffentlicht in:Nature communications 2013, Vol.4 (1), p.1525-1525, Article 1525
Hauptverfasser: Feaver, Ryan E., Gelfand, Bradley D., Blackman, Brett R.
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Sprache:eng
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Zusammenfassung:Haemodynamic variations are inherent to blood vessel geometries (such as bifurcations) and correlate with regional development of inflammation and atherosclerosis. However, the complex frequency spectrum characteristics from these haemodynamics have never been exploited to test whether frequency variations are critical determinants of endothelial inflammatory phenotype. Here we utilize an experimental Fourier transform analysis to systematically manipulate individual frequency harmonics from human carotid shear stress waveforms applied in vitro to human endothelial cells. The frequency spectrum, specifically the 0th and 1st harmonics, is a significant regulator of inflammation, including NF-κB activity and downstream inflammatory phenotype. Further, a harmonic-based regression-model predicts eccentric NF-κB activity observed in the human internal carotid artery. Finally, short interfering RNA-knockdown of the mechanosensor PECAM-1 reverses frequency-dependent regulation of NF-κB activity. Thus, PECAM-1 may have a critical role in the endothelium’s exquisite sensitivity to complex shear stress frequency harmonics and provide a mechanism for the focal development of vascular inflammation. Natural variations in blood flow haemodynamics are associated with localized inflammation and atherosclerosis. Here the authors show that individual harmonics present within this complex signal have distinct impacts on the inflammatory phenotype in endothelial cells.
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms2530