Hippocampal pyramidal cells: the reemergence of cortical lamination

The increasing resolution of tract-tracing studies has led to the definition of segments along the transverse axis of the hippocampal pyramidal cell layer, which may represent functionally defined elements. This review will summarize evidence for a morphological and functional differentiation of pyramidal cells along the radial (deep to superficial) axis of the cell layer. In many species, deep and superficial sublayers can be identified histologically throughout large parts of the septotemporal extent of the hippocampus. Neurons in these sublayers are generated during different periods of development. During development, deep and superficial cells express genes (Sox5, SatB2) that also specify the phenotypes of superficial and deep cells in the neocortex. Deep and superficial cells differ neurochemically (e.g. calbindin and zinc) and in their adult gene expression patterns. These markers also distinguish sublayers in the septal hippocampus, where they are not readily apparent histologically in rat or mouse. Deep and superficial pyramidal cells differ in septal, striatal, and neocortical efferent connections. Distributions of deep and superficial pyramidal cell dendrites and studies in reeler or sparsely GFP-expressing mice indicate that this also applies to afferent pathways. Histological, neurochemical, and connective differences between deep and superficial neurons may correlate with (patho-) physiological phenomena specific to pyramidal cells at different radial locations. We feel that an appreciation of radial subdivisions in the pyramidal cell layer reminiscent of lamination in other cortical areas may be critical in the interpretation of studies of hippocampal anatomy and function

Giant axonal neuropathy with subclinical involvement of the central nervous system: case report.

The case of a 17-year-old girl with slowly progressive sensory-motor neuropathy is described. Sural nerve biopsy showed abnormally enlarged exons filled with neurofilaments. Neurofilament accumulation was limited to the axons and was not found in other cells of the skin or peripheral nerve. The patient showed EEG and brain MRI abnormalities, but there was no clinical evidence of central nervous system involvement. Although these findings suggest an atypical attenuated form of giant axonal neuropathy, a new nosological entity cannot be excluded

A new monomeric α-amylase inhibitor from the tetraploid emmer wheat is mostly active against stored product pests

Abstract: The tetraploid domesticated emmer wheat, Triticum turgidum L. subsp. dicoccon, expresses α-amylase protein inhibitors of varying sizes and assemblies, i.e. dimers and heterotetramers of polypeptide chains of about 12–15 kDa. Although genetic studies have shown the presence of coding sequences for monomeric inhibitors in tetraploid wheat and whole-seeds proteomic studies have indicated their expression, until now there has been no isolation nor characterization of such proteins. In this study, for the first time, an inhibitory protein of human salivary and Tenebrio molitor, Tribolium castaneum, Sitophilus oryzae, and Ephestia kuehniella α-amylase (EC 3.2.1.1), was isolated from whole flour extracts of a tetraploid wheat and its sequence was determined by MS analyses. The inhibitor acts more strongly against coleopteran α-amylases than against those from E. kuheniella and human saliva. The inhibitory characteristics along with the putative sequence determination reported in the present study, allows for further evaluation towards its utilization as a post-harvest protection strategy against insect infestations. © 2021, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature