Nerve growth factor neuroprotection of ethanol-induced neuronal death in rat cerebral cortex is age dependent

Organotypic cultures of rat cortex were used to test the hypotheses that nerve growth factor (NGF) is neuroprotective for immature cortical neurons and that ethanol abolishes this neuroprotection in a developmental stage-dependent manner. Samples were obtained on gestational day (G) 16 or postnatal day (P) 3 and cultured with ethanol (0 or 400 mg/dl) and NGF (0 or 30 ng/ml) for 72 h. Dying neurons were identified as exhibiting terminal nick-end labeling, immunoreactivity for activated caspase 3, or condensed nuclear chromatin. Two cortical compartments were examined in fetal tissue: a superficial, cell-sparse marginal zone (MZ) and a cell-dense cortical plate (CP). At P3, the CP was subdivided into a cell-dense upper cortical plate (UCP) and a less densely packed lower cortical plate (LCP). Neuronal death in the MZ was affected by neither NGF nor ethanol at both ages. In the fetal CP, NGF did not affect the incidence of cell death, but ethanol increased it. Treatment with NGF caused an upregulation of the expression of Neg, a gene known to be affected by NGF and ethanol. NGF did not ameliorate the ethanol-induced death. In pups, ethanol increased the amount of death in the LCP. NGF did protect against this death. Neither ethanol nor NGF altered the incidence of cell death in the UCP. The laminar-dependent neuroprotection did not correlate with expression of NGF receptors or Neg. Thus, NGF can be protective against the neurotoxic effect of ethanol in the neonatal brain. This effect is site selective and time dependent and it targets postmigratory, differentiating neurons.     

Upregulation of glutamate receptors in rat cerebral cortex with neuronal migration disorders

Neuronal migration disorders (NMDs) constitute the main pathologic substrate of medically intractable epilepsy in human. This study is designed to investigate the changes in expression of glutamate receptor subtypes on radiation-induced NMD in rats. The lesion was produced by intrauterine irradiation (240 cGy) on E17 rats, and then 10 weeks old rats were used for the study. The pathologic and immuno-histochemical findings for glutamate receptor subunit proteins on NMD cortex were correlated with development of behavioral seizures and EEG abnormality. Spontaneous seizures uncommonly occurred in NMD rats (5%); however, clinical stages of seizures were significantly increased in NMD rats by an administration of kainic acid. Brains taken from irradiated rats revealed gross and histopathologic features of NMD. Focal cortical dysplasia was identified by histopathology and immunohistochemistry with neurofilament protein (NF-M/H). Significantly strong NR1 and NR2A/B immunoreactivities were demonstrated in cytomegalic and heterotopic neurons of NMD rats. The results of the present study indicate that epileptogenesis of NMD might be caused by upregulation of glutamate receptor expression in dysplastic neurons of the rat cerebral cortex with NMDs.     

Intramitochondrial crystalloid inclusions in neuronal processes of human cerebral cortex

Summary Orbital cortex specimens obtained as postmortem brain needle samples from 4 of 7 elderly subjects contained inclusion-carrying mitochondria in a small percentage of neuronal processes. Banded, lattice-like and hexagonal patterns were all seen in the inclusions. These patterns are thought to result from different planes of section through ordered aggregates of tubules. The crystalloid inclusions in mitochondria are tentatively regarded as a morphologic variant within the normal range, possibly brought about by some metabolic changes intervening, for instance, just before death.     

Characteristics of the functional organization of neuronal groups in functionally diverse zones of the human cerebral cortex from birth to 20 years of age

Using computer analysis of histological specimens of motor and posterior associative cortex of the man aged from birth up to 20 yrs age and individual peculiarities of focal groups sublayer III3 of areas 4p, 6op and 37ac, periods of intensive and slow growth of the area of profile fields (PF) of cell groups and total area (TA) of neurons in the group were established. It was shown that greater changes of cell groups PF area and neuron TA occurred in the area 4p during first 3 yrs, while in areas 6op and 37ac from birth up to 7 yrs and 8-9 yrs appropriately. Specific features of the group development in functionally different areas of human brain cortex was demonstrated.     

Chronic unpredictable stress promotes neuronal apoptosis in the cerebral cortex

Stress-mediated loss of synaptogenesis in the hippocampus appears to play a role in depressive and mood disorders. However, little is known about the effect of stress/depression on the plasticity and survival of cortical neurons. In this report, we have examined whether chronic stress increases the vulnerability of neurons in the rat cortex. We have used a chronic unpredictable mild stress (CMS) as a rat model of depression. CMS (5 weeks treatment) produced anedonia and increased corticosterone levels. These effects were accompanied by a detectable increase in caspase-3 positive neurons in the cerebral cortex, suggesting apoptosis. Desipramine (DMI), a well known antidepressant, reversed the pro-apoptotic effect of CMS. These results suggest that antidepressants may reduce the pathological changes seen in stress-induced depressive disorders.     

Ultrastructural pathology of neuronal membranes in the oedematous human cerebral cortex

Surgical biopsies of frontal, parietal and temporal regions of thirty two patients with clinical diagnosis of congenital hydrocephalus, brain trauma, tumours, and vascular anomalies were examined with the transmission electron microscope. The main goal was to study the submicroscopic alterations of somatodendritic, axonal, and synaptic plasma membranes, cytomembranes, and the cytoskeleton. In both, moderate and severe oedema, fragmentation of plasma membrane, enlargement and focal necrosis of rough endoplasmic cisterns and nuclear envelope, detachment of membrane-bound ribosomes and reduction of polysome were observed. The degenerated myelinated axons exhibited discontinuities of the axolemma, disorganisation of multiple myelin lamellae, myelin sheath vacuolization, and formation of myelin ovoids. In severe oedema, synaptic disassembly was frequently found characterized by separate pre- and postsynaptic endings and loss of perisynaptic glial ensheathment. Fragmented and intact microtubules and actin-like filaments also were distinguished. The alterations of plasma membranes and cytomembranes are related with the anoxic-ischaemic conditions of brain parenchyma. The role of free radical and lipid peroxidation, disturbed energy metabolism, altered metabolic cascades, excitotoxicity, protein aggregation, and presence of extracellular oedema fluid is discussed in relation with the derangement of neuronal membranes.     

The effect of aging on the neuronal population within area 17 of adult rat cerebral cortex

The brains of Sprague-Dawley rats in various age groups from 3 to 33 months were fixed by perfusion with standard aldehyde solutions in order to determine the effects of aging on neuronal numbers. Several indices of cortical volume were then measured to determine whether neuronal packing densities were affected by age-related change in cortical volume. The lengths, heights and widths of individual hemispheres for 160 animals ranging in age from 1 day to 36 months were first determined, after which blocks of tissue were removed from area 17 of some of the brains. These blocks were osmicated, embedded in Araldite and sectioned at 1 micrometer to ascertain, in the vertical plane, the thickness of area 17 and, in the tangential plane, the packing density of the clusters of apical dendrites extending from layer V pyramidal neurons. Results indicate the overall dimensions of the cerebral hemispheres increased until 3 months of age, after which there was no further increase in size. Between 3 and 33 months of age there was no age-related change in either the thickness of area 17 or in the separation between dendritic clusters, indicating the volume of area 17 did not change after 3 months of age. Within individual age groups the amount of variation present is greater than that among age groups. Since the number of nucleus-containing neuronal profiles per unit area of layers II/III, IV, V, VIa and VIb was similar in two groups of three animals at 3 and 33 months of age and the diameters of neuronal nuclei were unchanged, there seems to be no significant change in the number of neurons contained in these layers of rat visual cortex between 3 and 33 months of age. It is therefore concluded that no neurons are lost from area 17 as the mature cerebral cortex ages.     

N-cofilin is associated with neuronal migration disorders and cell cycle control in the cerebral cortex

Many neuronal disorders such as lissencephaly, epilepsy, and schizophrenia are caused by the abnormal migration of neurons in the developing brain. The role of the actin cytoskeleton in neuronal migration disorders has in large part remained elusive. Here we show that the F-actin depolymerizing factor n-cofilin controls cell migration and cell cycle progression in the cerebral cortex. Loss of n-cofilin impairs radial migration, resulting in the lack of intermediate cortical layers. Neuronal progenitors in the ventricular zone show increased cell cycle exit and exaggerated neuronal differentiation, leading to the depletion of the neuronal progenitor pool. These results demonstrate that mutations affecting regulators of the actin cytoskeleton contribute to the pathology of cortex development.     

The effect of aging on the neuronal population within area 17 of adult rat cerebral cortex

The brains of Sprague-Dawley rats in various age groups from 3 to 33 months were fixed by perfusion with standard aldehyde solutions in order to determine the effects of aging on neuronal numbers. Several indices of cortical volume were then measured to determine whether neuronal packing densities were affected by age-related change in cortical volume. The lengths, heights and widths of individual hemispheres for 160 animals ranging in age from 1 day to 36 months were first determined, after which blocks of tissue were removed from area 17 of some of the brains. These blocks were osmicated, embedded in Araldite and sectioned at 1 micrometer to ascertain, in the vertical plane, the thickness of area 17 and, in the tangential plane, the packing density of the clusters of apical dendrites extending from layer V pyramidal neurons. Results indicate the overall dimensions of the cerebral hemispheres increased until 3 months of age, after which there was no further increase in size. Between 3 and 33 months of age there was no age-related change in either the thickness of area 17 or in the separation between dendritic clusters, indicating the volume of area 17 did not change after 3 months of age. Within individual age groups the amount of variation present is greater than that among age groups. Since the number of nucleus-containing neuronal profiles per unit area of layers II/III, IV, V, VIa and VIb was similar in two groups of three animals at 3 and 33 months of age and the diameters of neuronal nuclei were unchanged, there seems to be no significant change in the number of neurons contained in these layers of rat visual cortex between 3 and 33 months of age. It is therefore concluded that no neurons are lost from area 17 as the mature cerebral cortex ages.     

Distinct neuronal populations specified to form corticocortical and corticothalamic projections from layer VI of developing cerebral cortex

Layer VI of the cerebral cortex contains heterogeneous populations of pyramidal neurons whose axons project either cortically or subcortically. It has been shown that a subset of layer VI neurons expressing latexin projects ipsilaterally to other cortical areas but does not contribute to the corticothalamic projections. Taking advantage of the connectional specificity of latexin-expressing neurons, we here determine whether corticocortical and corticothalamic neurons are generated at different times, and at which stage the connectional distinction develops in corticogenesis. Our experimental findings indicate that: (1) thalamic-projecting neurons in layer VI of the rat secondary somatosensory cortex (SII) are born at embryonic day 14 or before while latexin-expressing neurons in the same layer are generated at embryonic day 15 or later; (2) axonal invasion by SII neurons into ipsilateral cortical areas and into the posterior dorsal thalamus mainly takes place early in the postnatal period; (3) latexin-expressing neurons never project toward the dorsal thalamus in normal development; (4) presumptive latexin-expressing neurons in the neonatal SII are able to grow into a cortical slice in vitro, but do not invade a thalamic slice even transiently; (5) thalamic-projecting neurons, on the other hand, fail to simultaneously establish connections with a cortical slice. Taken together, our findings suggest that the time frame in which presumptive corticocortical and corticothalamic neurons are generated differs, and that the two populations are restricted in connectional fate potential by the perinatal period prior to target innervation.     

Quantitative changes in fibro-architectonics of the human cerebral cortex from birth to 12 years of age

The peculiarities of fibroarchitectonics in topographically and functionally distinct cortical zones (including temporo-parieto-occipital subarea, occipital, pre-, postcentral, and frontal areas) were studied in the brain specimens of 74 children of different ages (from birth to 12 years) taken with yearly intervals, while those in the first year of life--with monthly intervals. Frontal sections stained with Nissl, Peters and Golgi methods were studied using computer analysis of optical images. The data were obtained on the increment rates of radial fiber fascicles' thickness, distances between fascicles and age dynamics of ratios of volume densities of neurons and fibers in areas 3, 4p, 6op, 17, 19, 37ac, 44 and 32/10. It was shown that age-related transformations of fibroarchitectonics in the areas of sensomotor, somatosensory, occipital, temporo-parieto-occipital and frontal cortex were heterochronic and took place with different intensity; most pronounced changes were found to occur during the first 2-3 years, while less intensive ones were observed up to the age of 9-12 years.     

Gallium nitride induces neuronal differentiation markers in neural stem/precursor cells derived from rat cerebral cortex

In the present study, gallium nitride (GaN) was used as a substrate to culture neural stem/precursor cells (NSPCs), isolated from embryonic rat cerebral cortex, to examine the effect of GaN on the behavior of NSPCs in the presence of basic fibroblast growth factor (bFGF) in serum-free medium. Morphological studies showed that neurospheres maintained their initial shape and formed many long and thick processes with the fasciculate feature on GaN. Immunocytochemical characterization showed that GaN could induce the differentiation of NSPCs into neurons and astrocytes. Compared to poly-d-lysine (PDL), the most common substrate used for culturing neurons, there was considerable expression of synapsin I for differentiated neurons on GaN, suggesting GaN could induce the differentiation of NSPCs towards the mature differentiated neurons. Western blot analysis showed that the suppression of glycogen synthase kinase-3β (GSK-3β) activity was one of the effects of GaN-promoted NSPC differentiation into neurons. Finally, compared to PDL, GaN could significantly improve cell survival to reduce cell death after long-term culture. These results suggest that GaN potentially has a combination of electric characteristics suitable for developing neuron and/or NSPC chip systems.     

Features of the ensemble organization of the human cerebral cortex from birth to 20 years of age

Translated from Arkhiv Anatomii, Gistologii i Émbriologii, Vol. 97, No. 12, pp. 15–24, December, 1989.     

Human neuronal calcium sensor-1 shows the highest expression level in cerebral cortex

Neuronal calcium sensors (NCS) are important constituents in the intracellular signaling pathways. A novel human gene, NCS-1, was identified in the present study. Among the 16 human tissues examined, NCS-1 is expressed most abundantly in the brain. Among the brain regions, the expression level of NCS-1 in cerebral cortex is the highest, which is about six times higher than the average level of the whole brain and a hundred times higher than the spinal cord. In the 12 different anatomical regions of human brain, the expression level of NCS-1 is very high in the temporal lobe, occipital pole, frontal lobe, thalamus, amygdala and hippocampus; moderate in cerebellum, putamen, caudate nucleus; low in the medulla, substantia nigra and the lowest in corpus callosum. Our results suggest that NCS-1 in human brain might be involved in a variety of brain functions such as sensory processing, motor control, emotional control, learning and memory.     

Fos expression and task-related neuronal activity in rat cerebral cortex after instrumental learning

Learning has been shown to induce changes in neuronal gene expression and to produce development of task-specific neuronal activity. The connection between these two features of neuronal plasticity remains of a great interest. To address this issue we compared distribution of c-Fos expressing and task-related neurons in the rat cerebral cortex following instrumental learning of appetitive lever-press task. The number of Fos-positive neurons was determined immunohistochemically in the retrosplenial and the motor cortex of naive ("control" group), newly trained ("acquisition" group) and overtrained ("performance" group) animals. A significant activation of c-Fos expression was observed in the neurons of the retrosplenial but not motor cortex in the "acquisition" group rats, as compared with the "control" and "performance" groups. In accordance with this c-Fos expression difference, the retrosplenial cortex of the trained animals contained significantly more neurons with lever-press-related activity than the motor cortex. Therefore, the two examined cortical areas showed a parallel between experience-dependent induction of c-Fos and development of task-related neuronal activity. These data support a notion that learning-induced activation of c-Fos is associated with long-term neurophysiological changes produced by training.     

The carboxylmethylation of cerebral membrane-bound proteins increases with age

Recently, we have characterized a membrane-bound (mb) component of brain protein carboxylmethyltransferase II (PCMT) which effectively carboxylmethylates endogenous mb methyl-accepting proteins (MAPs). (Neurochem. Int., 10 (1987) 155). We have also shown that exposing mb-MAPs to mild alkali leads to a marked increase in their recognition by PCMT. Since one of the likely consequences of the alkaline treatment appears to be the deamidation of selected protein-bound asparagines or aspartates, followed by the formation, in their place, of D-or L-isoaspartates, it is reasonable to assume that mb-MAPs constitute unique targets for the mb-PCMT because they contain such unnatural aspartate residues. Testing the relevance of this notion to the aging of cerebral mb-MAPs we focus in this report on age-related changes involving mb-MAPs. When two-or six-times washed (in 50 mM NaPO4 buffer, pH 6.5) 17,500 g, 30-min membranes or Percoll-gradient purified synaptic membranes were prepared from young (3-4 months) and old (11-12 months) rat brains and were incubated with 20 microM [3H]methyl S-adenosyl-L-methionine at pH 6.0, mb-MAP carboxyl[3H]methylation was significantly more intense in the old than in the young membranes, no additional increase being noted at 28-35 months. Mb-MAP carboxylmethylation increases were confirmed over a wide range of membrane protein concentrations and incubation times and are taken to reflect age-related modifications of the primary structure of susceptible mb-MAPs. To investigate these, we incubated young and old membranes, as well as their Lubrol-Px (1%) extracts (30 min, 0 degree C), with 0.05 M NH4OH for 90 min at 37 degrees C, a treatment which left PCMT activity largely unaffected. Our findings reveal that the effect of the NH4OH treatment on the generation of carboxylmethylatable sites was markedly smaller in "old" than in "young" proteins, suggesting that "new" carboxylmethylatable sites are generated in susceptible mb-MAPs in situ, by a process accompanying, or otherwise marking, the natural aging of neural membrane proteins.