Antagonism of a key peptide 'T14' driving neurodegeneration: Evaluation of a next generation therapeutic.

T14, a 14mer peptide derived from the C-terminus of acetylcholinesterase (AChE) is a signalling molecule that could drive neurodegeneration via the alpha 7 nicotinic acetylcholine receptor. Its levels increase as Alzheimer's pathology progresses; however, a cyclic variant of the compound, NBP14, can block the effects of the endogenous linear counterpart in-vitro, ex vivo, and in vivo. Here, we explore the antagonistic potential of two 6mer peptides, NBP6A and NBP6B.

Diversity in striatal synaptic circuits arises from distinct embryonic progenitor pools in the ventral telencephalon.

Synaptic circuits in the brain are precisely organized, but the processes that govern this precision are poorly understood. Here, we explore how distinct embryonic neural progenitor pools in the lateral ganglionic eminence contribute to neuronal diversity and synaptic circuit connectivity in the mouse striatum. In utero labeling of Tα1-expressing apical intermediate progenitors (aIP), as well as other progenitors (OP), reveals that both progenitors generate direct and indirect pathway spiny projection neurons (SPNs) with similar electrophysiological and anatomical properties and are intermingled in medial striatum.

The perception of three-dimensional cast-shadow structure is dependent on visual awareness.

In the present study we examined whether the perception of depth from cast shadows is dependent on visual awareness using continuous flash suppression (CFS). As a direct measure of how the visual system infers depth from cast shadows, we examined the cast-shadow motion illusion originally reported by Kersten, Knill, Mamassian, and Bulthoff (1996), in which a moving cast shadow induces illusory motion in depth in a physically stationary object. In Experiment 1, we used a disparity defined probe to determine the stereo motion speed required to match the cast-shadow motion illusion for different cast shadow speeds (0°/s-1.