Cell Type-Specific Differences in Spike Timing and Spike Shape in the Rat Parasubiculum and Superficial Medial Entorhinal Cortex.

The medial entorhinal cortex (MEC) and the adjacent parasubiculum are known for their elaborate spatial discharges (grid cells, border cells, etc.) and the precessing of spikes relative to the local field potential. We know little, however, about how spatio-temporal firing patterns map onto cell types.

Functional Architecture of the Rat Parasubiculum.

Unlabelled: The parasubiculum is a major input structure of layer 2 of medial entorhinal cortex, where most grid cells are found. Here we investigated parasubicular circuits of the rat by anatomical analysis combined with juxtacellular recording/labeling and tetrode recordings during spatial exploration. In tangential sections, the parasubiculum appears as a linear structure flanking the medial entorhinal cortex mediodorsally.

Cell-Type Specific Phase Precession in Layer II of the Medial Entorhinal Cortex.

Unlabelled: The identity of phase-precessing cells in the entorhinal cortex is unknown. Here, we used a classifier derived from cell-attached recordings to separate putative pyramidal cells and putative stellate cells recorded extracellularly in layer II of the medial entorhinal cortex in rats. Using a novel method to identify single runs as temporal periods of elevated spiking activity, we find that both cell types show phase precession but putative stellate cells show steeper slopes of phase precession and larger phase ranges.

Head-Directional Tuning and Theta Modulation of Anatomically Identified Neurons in the Presubiculum.

Unlabelled: The presubiculum provides a major input to the medial entorhinal cortex (MEC) and contains cells that encode for the animal's head direction (HD), as well as other cells likely to be important for navigation and memory, including grid cells. To understand the mechanisms underlying HD cell firing and its effects on other parts of the circuit, it is important to determine the anatomical identity of these functionally defined cells. Therefore, we juxtacellularly recorded single cells in the presubiculum in freely moving rats, finding two classes of cells based on firing patterns and juxtacellular labeling (of a subset).

Anatomical Organization and Spatiotemporal Firing Patterns of Layer 3 Neurons in the Rat Medial Entorhinal Cortex.

Layer 3 of the medial entorhinal cortex is a major gateway from the neocortex to the hippocampus. Here we addressed structure-function relationships in medial entorhinal cortex layer 3 by combining anatomical analysis with juxtacellular identification of single neurons in freely behaving rats. Anatomically, layer 3 appears as a relatively homogeneous cell sheet.

Pyramidal and stellate cell specificity of grid and border representations in layer 2 of medial entorhinal cortex.

In medial entorhinal cortex, layer 2 principal cells divide into pyramidal neurons (mostly calbindin positive) and dentate gyrus-projecting stellate cells (mostly calbindin negative). We juxtacellularly labeled layer 2 neurons in freely moving animals, but small sample size prevented establishing unequivocal structure-function relationships. We show, however, that spike locking to theta oscillations allows assigning unidentified extracellular recordings to pyramidal and stellate cells with ∼83% and ∼89% specificity, respectively.

Juxtacellular recording and morphological identification of single neurons in freely moving rats.

It is well established that neural circuits consist of a great diversity of cell types, but very little is known about how neuronal diversity contributes to cognition and behavior. One approach to addressing this problem is to directly link cellular diversity to neuronal activity recorded in vivo in behaving animals. Here we describe the technical procedures for obtaining juxtacellular recordings from single neurons in trained rats engaged in exploratory behavior.

Grid-layout and theta-modulation of layer 2 pyramidal neurons in medial entorhinal cortex.

Little is known about how microcircuits are organized in layer 2 of the medial entorhinal cortex. We visualized principal cell microcircuits and determined cellular theta-rhythmicity in freely moving rats. Non-dentate-projecting, calbindin-positive pyramidal cells bundled dendrites together and formed patches arranged in a hexagonal grid aligned to layer 1 axons, parasubiculum, and cholinergic inputs.

An isomorphic mapping hypothesis of the grid representation.

We introduce a grid cell microcircuit hypothesis. We propose the 'grid in the world' (evident in grid cell discharges) is generated by a 'grid in the cortex'. This cortical grid is formed by patches of calbindin-positive pyramidal neurons in layer 2 of medial entorhinal cortex (MEC).

[Cloning of the gene encoding alpha-glucosidase from aspergillus niger and its expression in Pichia pastoris].

Objective: Alpha-glucosidase from Aspergillus niger SG136 was expressed in Pichia pastoris.

Methods: cDNA of mature alpha-glucosidase (aglu) was amplified from the total DNA of A. niger SG136 by PCR and overlap-PCR with primers designed based on the sequence of A.