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- Ekström, Peter, et al.
(author)
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Pineal neurons projecting to the brain of the rainbow trout, Salmo gairdneri Richardson (Teleostei) - In-vitro retrograde filling with horseradish peroxidase
- 1985
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In: Cell and Tissue Research. - 0302-766X. ; 240:3, s. 693-700
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Journal article (peer-reviewed)abstract
- The morphology of intrapineal neurons that give rise to the pineal tract and project to the brain in the rainbow trout was visualized by the use of neuronal backfilling with horseradish peroxidase (HRP). The tracing was performed on excised pineal organs under in-vitro conditions at 4° C, with filling times ranging from 6 to 24 h. Large multipolar, bipolar and unipolar neurons were visualized in the rostral tip of the pineal organ ("pineal ganglion"). These neurons possessed extended dendritic trees participating in the formation of a circumscribed neuropil-like area. Throughout the pineal organ small bipolar elements were the most ubiquitous type of neuron, however, with markedly smaller numbers in the proximal portion of the pineal end-vesicle. In the pineal stalk, some bipolar neurons were observed to contact the pineal lumen, which is continuous with the third ventricle, via dendritic processes of various types. It could not be established whether any of these CSF-contacting processes were identical with photoreceptor outer segments. The basal processes of the bipolar neurons sometimes possessed distally projecting collaterals. In conclusion, it has been shown that (i) different types of neurons displaying varied patterns of regional distribution contribute to the pineal tract, and (ii) certain CSF-contacting neurons in the pineal organ send axonal processes directly toward the brain.
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- Stavridis, Stavros I., et al.
(author)
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Cocultures of rat sensorimotor cortex and spinal cord slices to investigate corticospinal tract sprouting
- 2009
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In: Spine. - 0362-2436 .- 1528-1159. ; 34:23, s. 2494-2499
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Journal article (peer-reviewed)abstract
- STUDY DESIGN: Experimental study of corticospinal axonal sprouting in an organotypic slice culture model. OBJECTIVE: To develop an in vitro model that simplifies the study of various factors regulating neuronal regeneration. SUMMARY OF BACKGROUND DATA: Spinal cord injury leads to permanent neurologic damage, mainly due to the inability of the adult central nervous system to regenerate. Much attention has been focused on promoting axonal regeneration and sprouting, either by exogenous administration of various neurotrophic factors or by the antagonization of factors inhibiting regeneration. METHODS: An in vitro system that allows coculture of slices from rat sensorimotor cortex and spinal cord (p4) was established. Two groups of cultures were investigated: In the first group, intact spinal cord slices were cultured adjacent to sensorimotor cortex slices, while in the second group the spinal cord slices were sagittally cut into halves, with the sectioned interface placed directly adjacent to the sensorimotor cortex, to prevent the spinal white matter from interference. Each group was further divided into 2 subgroups: The neurotrophin-3 (NT-3) group, where the culture medium contained 50 ng/mL NT-3 and the control group treated with normal culture medium. Sensorimotor cortex pyramidal neurons were anterogradely labeled with Mini-Ruby, a 10 kD biotinylated dextran amine. RESULTS: Cocultures of cortical and spinal cord tissue were propagated in vitro, and axonal sprouting occurred. The group of cocultures treated with NT-3 showed an improved cortical cytoarchitecture, and sprouting axons were more frequently observed. In NT-3-treated cocultures where spinal cord gray matter was directly opposed to cortical slices sprouting axons entered the adjacent spinal cord tissue. This phenomenon was not observed if spinal cord pia mater and white matter were opposed to the cortical slices, or if NT-3 was absent. CONCLUSION: Our data suggest that the absence of repellent factors such as white matter and the presence of neurotrophic factors promote axonal sprouting. Cocultures of sensorimotor cortex and spinal cord slices combined with anterograde axonal labeling could provide a valuable in vitro model for the simplified screening of factors influencing corticospinal tract regeneration.
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- Vogt, Cornelia, et al.
(author)
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Successful inhibition of excitotoxic neuronal damage and microglial activation after delayed application of interleukin-1 receptor antagonist
- 2008
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In: Journal of Neuroscience Research. - : Wiley. - 0360-4012 .- 1097-4547. ; 86:15, s. 3314-21
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Journal article (peer-reviewed)abstract
- Interleukin (IL)-1 is an important mediator of neuronal demise and glial activation after acute central nervous system lesions and is antagonized by IL-1 receptor antagonist (IL-1RA). Here we determined the time window in which IL-1RA elicits neuroprotective effects in rat organotypic hippocampal slice cultures (OHSC). OHSC were lesioned with N-methyl-D-aspartate (NMDA) and treated with IL-1RA (100 ng/ml) at different time points postinjury or were left untreated. Damaged neurons, microglial cells, and astrocytes were labelled with NeuN, propidium iodide, isolectin B(4), or glial fibrillary acidic protein (GFAP), respectively, and were analyzed by confocal laser scanning microscopy. In lesioned OHSC, the most dramatic increase in microglial cell number occurred between 8 and 16 hr postinjury, and the maximal neuronal demise was found between 16 and 24 hr postinjury. The cellular source of IL-1beta was investigated by immunohistochemistry, and IL-1beta immunoreactivity was found in few microglial cells at 4 hr postinjury and in numerous microglial cells and astrocytes at 16 hr postinjury. In both glial populations, IL-1beta immunoreactivity peaked at 24 hr postinjury. IL-1RA treatment potently suppressed neuronal damage by 55% when initiated within the first 16 hr postinjury (P < 0.05), and IL-1RA treatment initiated at 24 hr postinjury resulted in weaker but still significant neuroprotection. IL-1RA treatment also reduced the number of microglial cells significantly when initiated within 36 hr postinjury (P < 0.05). In conclusion, IL-1RA exhibits significant neuroprotective effects in this in vitro model of excitotoxic injury even after delayed application.
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