Aortic valve calcification is a common disease in the elderly, but its cellular and molecular mechanisms are not clear. In order to verify the hypothesis that Wnt/β-catenin signaling pathway is involved in the process of calcification of aortic valve, porcine aortic valve interstitial cells (VICs) were isolated, cultured and stimulated with oxidized low density lipoprotein (ox-LDL) for 48 h to induce the differentiation of VICs into osteoblast-like cells. The key proteins and genes of Wnt/β-catenin signaling pathway, such as glycogen synthase kinase 3β (GSK-3β) and β-catenin, were detected by using Western blotting and real-time polymerase chain reaction (PCR). The results showed that the VICs managed to differentiate into osteoblast-like cells after the stimulation with ox-LDL and the levels of proteins and genes of GSK-3β and β-catenin were increased significantly in VICs after stimulation for 48 h (P<0.05). It is suggested that Wnt/β-catenin signaling pathway may play a key role in the differentiation of VICs into osteoblast-like cells and make great contribution to aortic valve calcification.
We report on the development of a 250-MHz 234 nm deep-ultraviolet pulse source based on a flexible wavelength-conversion scheme. The scheme is based on a frequency-doubled optical parametric oscillator (FD-OPO) together with a cascaded frequency conversion process. We use a χ(2) nonlinear envelope equation to guide the design of an intra-cavity OPO crystal, demonstrating a flexible broadband tunable feature and providing as high as watt-level of a frequency-doubled signal output centered at 850 nm, which is served as an input wave for the cascaded frequency conversion process. As much as 3.0 mW of an average power at 234 nm is obtained, with an rms power stability of better than 1% over 20 minutes. This deep-ultraviolet pulse laser source can be used for many applications in quantum optics and for direct laser cooling of Al+ ion clocks.
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