10 research outputs found
Heat transfer through the interface and flow regimes in liquid bridge subjected to co-axial gas flow
We present results of an extensive numerical study on the thermocapillary (Marangoni) convection and a heat transfer through the interface in a liquid bridge of Pr = 68. The geometry of the physical problem is a cylindrical and non-deformable liquid bridge concentrically surrounded by an annular gas channel under conditions of zero gravity. The gas flow is co- or counter-directed with respect to the Marangoni flow. The forced gas flow along the interface provides two actions: via shear stresses and heat exchange. Usually the cooling of the interface enhances the flow while the heating slows down. This general trend may not hold when shear and thermocapillary stresses are comparable. The results show that when gas enters from the cold side the heat transfer through the interface is considerably larger than that when gas enters from the hot side. © Springer Science+Business Media B.V. 2012.SCOPUS: ar.jinfo:eu-repo/semantics/publishe
Ubiquitous transient stagnant domain formation during thermal convection in a well-mixed two component fluid with large viscosity difference
Onset and Nonlinear Regimes of Convection of a Binary Mixture in Rectangular Cavity Heated from Below
PAN-811 prevents chemotherapy-induced cognitive impairment and preserves neurogenesis in the hippocampus of adult rats
The mechanism of sirtuin 2–mediated exacerbation of alpha-synuclein toxicity in models of Parkinson disease
Sirtuin genes have been associated with aging and are known to affect multiple cellular pathways. Sirtuin 2 was previously shown to modulate proteotoxicity associated with age-associated neurodegenerative disorders such as Alzheimer and Parkinson disease (PD). However, the precise molecular mechanisms involved remain unclear. Here, we provide mechanistic insight into the interplay between sirtuin 2 and α-synuclein, the major component of the pathognomonic protein inclusions in PD and other synucleinopathies. We found that α-synuclein is acetylated on lysines 6 and 10 and that these residues are deacetylated by sirtuin 2. Genetic manipulation of sirtuin 2 levels in vitro and in vivo modulates the levels of α-synuclein acetylation, its aggregation, and autophagy. Strikingly, mutants blocking acetylation exacerbate α-synuclein toxicity in vivo, in the substantia nigra of rats. Our study identifies α-synuclein acetylation as a key regulatory mechanism governing α-synuclein aggregation and toxicity, demonstrating the potential therapeutic value of sirtuin 2 inhibition in synucleinopathies.Open-Access-Publikationsfonds 2017peerReviewe
