Biomedical subjects

Frank Schottler

Publications and source records attributed to Frank Schottler.

3 recordsLinked to original sources

PubMed2006

A new planar multielectrode array: recording from a rat auditory cortex.

In the study of the spatiotemporal properties of the cortex, a demand often arises for recording local field evoked potentials (LFEP) and neural spikes from a quantity of points at close range from each other. In such a situation a device composed of a lot of electrodes assembled in a single bunch would be suitable. Such circumstances gave us the impetus to create the device described in this paper, namely a new planar electrode array for in vivo multisite extracellular recording. The device is made of plastic and includes platinum electrodes 50 microm in diameter. The array of 64 incorporated microelectrodes is placed on the surface of the cortex of anesthetized rats. Recordings could be made through all electrodes for more than 1 h without damage to the cortex. The inter-polar distance is approximately 100 microm so that each individual electrode can record activity from a separate population of neurons near the cortical surface. The recording system described here is highly useful for visualizing spatiotemporal structure of the cortical activities and for imaging dynamic neuronal assemblies.

Acoustic Stimulation↗

PubMed2006

Bcl-2 over-expression fails to prevent age-related loss of calretinin positive neurons in the mouse dentate gyrus.

BACKGROUND: Cognitive performance declines with increasing age. Possible cellular mechanisms underlying this age-related functional decline remain incompletely understood. Early studies attributed this functional decline to age-related neuronal loss. Subsequent studies using unbiased stereological techniques found little or no neuronal loss during aging. However, studies using specific cellular markers found age-related loss of specific neuronal types. To test whether there is age-related loss of specific neuronal populations in the hippocampus, and subsequently, whether over-expression of the B-cell lymphoma protein-2 (Bcl-2) in these neurons could delay possible age-related neuronal loss, we examined calretinin (CR) positive neurons in the mouse dentate gyrus during aging. RESULT: In normal mice, there was an age-related loss of CR positive cells in the dentate gyrus. At the same region, there was no significant decrease of total numbers of neurons, which suggested that age-related loss of CR positive cells was due to the decrease of CR expression in these cells instead of cell death. In the transgenic mouse line over-expressing Bcl-2 in neurons, there was an age-related loss of CR positive cells. Interestingly, there was also an age-related neuronal loss in this transgenic mouse line. CONCLUSION: These data suggest an age-related loss of CR positive neurons but not total neuronal loss in normal mice and this age-related neuronal change is not prevented by Bcl-2 over-expression.

Journal Article↗

PubMedDate not supplied

Transplantation of apoptosis-resistant embryonic stem cells into the injured rat spinal cord.

Murine embryonic stem cells were induced to differentiate into neural lineage cells by exposure to retinoic acid. Approximately one million cells were transplanted into the lesion site in the spinal cords of adult rats which had received moderate contusion injuries 9 days previously. One group received transplants of cells genetically modified to over-express bcl-2, which codes for an anti-apoptotic protein. A second group received transplants of the wild-type ES cells from which the bcl-2 line was developed. In the untransplanted control group, only medium was injected. Locomotor abilities were assessed using the Basso, Beattie and Bresnahan (BBB) rating scale for 6 weeks. There was no incremental locomotor improvement in either transplant group when compared to control over the survival period. Morbidity and mortality were significantly more prevalent in the transplant groups than in controls. At the conclusion of the 6-week survival period, the spinal cords were examined. Two of six cords from the bcl-2 group and one of 12 cords from the wild-type group showed gross evidence of abnormal growths at the site of transplantation. No similar growth was seen in the control. Pathological examination of the abnormal cords showed very large numbers of undifferentiated cells proliferating at the injection site and extending up to 1.5 cm rostrally and caudally. These results suggest that transplanting KD3 ES cells, or apoptosis-resistant cells derived from the KD3 line, into the injured spinal cord does not improve locomotor recovery and can lead to tumor-like growth of cells, accompanied by increased debilitation, morbidity and mortality.

Animals↗