Stochastic Generation of Particle Structures with Controlled Degree of Heterogeneity

The recently developed void expansion method (VEM) allows for an efficient generation of porous packings of spherical particles over a wide range of volume fractions. The method is based on a random placement of the structural particles under addition of much smaller "void-particles" whose radii are repeatedly increased during the void expansion. Thereby, they rearrange the structural particles until formation of a dense particle packing and introduce local heterogeneities in the structure. In this paper, microstructures with volume fractions between 0.4 and 0.6 produced by VEM are analyzed with respect to their degree of heterogeneity (DOH). In particular, the influence of the void- to structural particle number ratio, which constitutes a principal VEM-parameter, on the DOH is studied. The DOH is quantified using the pore size distribution, the Voronoi volume distribution and the density-fluctuation method in conjunction with fit functions or integral measures. This analysis has revealed that for volume fractions between 0.4 and 0.55 the void-particle number allows for a quasi-continuous adjustment of the DOH. Additionally, the DOH-range of VEM-generated microstructures with a volume fraction of 0.4 is compared to the range covered by microstructures generated using previous Brownian dynamics simulations, which represent the structure of coagulated colloidal suspensions. Both sets of microstructures cover similarly broad and overlapping DOH-ranges, which allows concluding that VEM is an efficient method to stochastically reproduce colloidal microstructures with varying DOH.Comment: 10 pages, 7 figure

Microstructures and Mechanical Properties of Dense Particle Gels: Microstructural Characterization

The macroscopic mechanical properties of densely packed coagulated colloidal particle gels strongly depend on the local arrangement of the powder particles on length scales of a few particle diameters. Heterogeneous microstructures exhibit up to one order of magnitude higher elastic properties and yield strengths than their homogeneous counterparts. The microstructures of these gels are analyzed by the straight path method quantifying quasi-linear particle arrangements of particles. They show similar characteristics than force chains bearing the mechanical load in granular material. Applying this concept to gels revealed that heterogeneous colloidal microstructures show a significantly higher straight paths density and exhibit longer straight paths than their homogeneous counterparts.Comment: 7 pages, 9 figure

Dietary exposure to PCBs and dioxins.

comments on S. Patandin et al. : Dietary exposure to polychlorinated biphenyls and dioxins from infancy until adulthood: a comparison between breast-feeding, toddler, and long-term exposure. Environ Health Perspect 107:45-51 (1999)

Impact of alpha-synuclein spreading on the nigrostriatal dopaminergic pathway depends on the onset of the pathology

Misfolded alpha-synuclein spreads along anatomically connected areas through the brain, prompting progressive neurodegeneration of the nigrostriatal pathway in Parkinson's disease. To investigate the impact of early stage seeding and spreading of misfolded alpha-synuclein along with the nigrostriatal pathway, we studied the pathophysiologic effect induced by a single acute alpha-synuclein preformed fibrils (PFFs) inoculation into the midbrain. Further, to model the progressive vulnerability that characterizes the dopamine (DA) neuron life span, we used two cohorts of mice with different ages: 2-month-old (young) and 5-month-old (adult) mice. Two months after a-synuclein PFFs injection, we found that striatal DA release decreased exclusively in adult mice. Adult DA neurons showed an increased level of pathology spreading along with the nigrostriatal pathway accompanied with a lower volume of alpha-synuclein deposition in the midbrain, impaired neurotransmission, rigid DA terminal composition, and less microglial reactivity compared with young neurons. Notably, preserved DA release and increased microglial coverage in the PFFs-seeded hemisphere coexist with decreased large-sized terminal density in young DA neurons. This suggests the presence of a targeted pruning mechanism that limits the detrimental effect of alpha-synuclein early spreading. This study suggests that the impact of the pathophysiology caused by misfolded alpha-synuclein spreading along the nigrostriatal pathway depends on the age of the DA network, reducing striatal DA release specifically in adult mice

Generation of Porous Particle Structures using the Void Expansion Method

The newly developed "void expansion method" allows for an efficient generation of porous packings of spherical particles over a wide range of volume fractions using the discrete element method. Particles are randomly placed under addition of much smaller "void-particles". Then, the void-particle radius is increased repeatedly, thereby rearranging the structural particles until formation of a dense particle packing. The structural particles' mean coordination number was used to characterize the evolving microstructures. At some void radius, a transition from an initially low to a higher mean coordination number is found, which was used to characterize the influence of the various simulation parameters. For structural and void-particle stiffnesses of the same order of magnitude, the transition is found at constant total volume fraction slightly below the random close packing limit. For decreasing void-particle stiffness the transition is shifted towards a smaller void-particle radius and becomes smoother.Comment: 9 pages, 8 figure

Neurogenesis from Sox2 expressing cells in the adult cerebellar cortex

We identified a rare undifferentiated cell population that is intermingled with the Bergmann glia of the adult murine cerebellar cortex, expresses the stem cell markers Sox2 and Nestin, and lacks markers of glial or neuronal differentiation. Interestingly, such Sox2(+) S100(-) cells of the adult cerebellum expanded after adequate physiological stimuli in mice (exercise), and Sox2(+) precursors acquired positivity for the neuronal marker NeuN over time and integrated into cellular networks. In human patients, SOX2(+) S100(-) cells similarly increased in number after relevant pathological insults (infarcts), suggesting a similar expansion of cells that lack terminal glial differentiation