Glial Cell-enriched Fractions Research Articles

Antioxidant enzymatic system in neuronal and glial cells enriched fractions of rat brain after aluminum exposure.

The aim of this work was to investigate as to how neurons and glial cells separated from the brain cortex respond to oxidative stress induced by aluminum. Female SD rats were exposed to aluminum at the dose level of 100 mg/kg b.w. for 8 weeks. Neuronal and glial cell-enriched fractions were obtained from rat cerebral cortex by sieving the trypsinated homogenate through a series of nylon meshes, followed by centrifugation on ficoll density gradient. Total glutathione content, glutathione peroxidase (GPx), glutathione reductase (GR), and glutathione-s-transferase (GST) along with antioxidant enzymes superoxide dismutase (SOD), catalase were estimated in neuronal and glial-enriched fractions in both control (N-c and G-c) and aluminum exposed animals (N-a and G-a). Secondary products of lipid peroxidation that is MDA levels were estimated by measuring the (TBARS) levels. Our results indicate that TBARS levels were significantly higher in glial cell fraction of unexposed controls (Gc) than the neuronal cells (Nc). Correspondingly the glial cells had higher levels of GSH, GSSG, GPx and GST where as neurons had higher levels of catalase, SOD and GR. Following aluminum exposures significant increase in the TBARS levels was observed in neurons as compared to glial cells which also showed a significant decrease in SOD and catalase activity. The decrease in the TBARS levels in the glial cells could be related to the increase in the GSH levels, GR activity, and GST activity which were found to be increased in glial enriched fractions following aluminum exposure. The increase in activity of various enzymes viz GR, GST in glial cells as compared to neurons suggests that glial cells are actively involved in glutathione homeostasis. Our conclusion is that glial and neurons isolated from rat cerebral cortex show a varied pattern of important antioxidant enzymes and glial cells are more capable of handling the oxidative stress conditions.

Oxidative events in neuronal and glial cell-enriched fractions of rat cerebral cortex

The aim of this work was to investigate how neurons and glial cells separated from rat brain cortex respond to “in vitro” oxidative stress induced by incubation of the cellular fractions in the presence of prooxidant mixtures; in addition, the endogenous enzymatic antioxidant capacity of the purified fractions was investigated. Neuronal and glial cell-enriched fractions were obtained from rat cerebral cortex following passages of the tissue through meshes and centrifugations. The following parameters were evaluated: antioxidant enzymes superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GSHPx), and glucose-6-phosphate dehydrogenase (G6PDH); lipid peroxidation products (TBARS) prior to (basal) and after (iron-stimulated) incubation with a mixture of iron and ascorbic acid; intracellular production of reactive oxygen species (ROS) using a fluorescent probe, dichlorofluorescin-diacetate, in basal, iron-stimulated, and menadione stimulated conditions. SOD and GSHPx activities showed no significant changes between neurons and glia, whereas CAT and G6PDH activities were found to be significantly lower in glia than in neurons. TBARS levels were significantly lower in the glial fraction than in neurons, both in basal and iron-stimulated conditions. ROS production showed no differences between neurons and glia in both basal and menadione-stimulated conditions. Iron-stimulation produced a marked increase in ROS production, limited to the neuronal fraction, with the glial values being similar to the basal ones. Our conclusion is that glia and neurons isolated from rat cerebral cortex show a similar pattern of the most important antioxidant enzymes and of their basal ROS production, whereas glia is more resistant in “oxidative stress” conditions.

Antioxidant enzymatic systems in neuronal and glial cell-enriched fractions of rat brain during aging

The activities of Cu,Zn superoxide dismutase, glutathione peroxidase, catalase and glutathione reductase in neuronal and glial cell-enriched fractions obtained from the cerebral cortex of rat brain during aging (15, 30, 90, 350, 750 days of age) were assayed. Our results showed that glutathione peroxidase, catalase and glutathione reductase activities varied little during the examined periods. Only the Cu,Zn superoxide dismutase activity decreased notably from 15th to 750th day of age in both neuronal and glial cells, moreover the activities of all enzymes studied were always detected at lower levels in neuronal cells with respect to glial cells. In agreement with diminished SOD activity, the lipid peroxidation showed an elevated increase with aging; this fact is more evident in neuronal than in glial cells. In conclusion our data show that Cu,Zn superoxide dismutase is the most affected antioxidant enzymatic system of brain aging and it could be responsible for the increased lipid peroxidation in both cell types examined.

Regional, cellular, and subcellular distribution of Thy-1 antigen in rat nervous tissues.

The regional, cellular, and subcellular distribution of Thy-1 antigen in rat nervous tissues was investigated with rabbit and anti-rat thymus antiserum. Thy-1 antigen was found most abundantly in the cerebrum, including the cerebral cortical layer, caudate nucleus, thalamus, and hypothalamus, and in the midbrain. It was found in lower amounts in the pons, medulla oblongata, cerebellum, and spinal cord. The content of Thy-1 antigen, however, was low in the retina, cervical sympathetic ganglion, and sciatic nerve, and there was little in the pineal body and adrenal medulla. Thy-1 antigen was present in the neuronal cell-enriched fraction, whereas the glial cell-enriched fraction lacked Thy-1 antigen. In a subcellular fractionation study, Thy-1 antigen was found to occur mainly in the synaptosomal membrane and microsomes and was low in the highly purified myelin fraction. The amount of Thy-1 antigen in the cerebral synaptosomal fraction was much higher than those in the cerebellar synaptosomal fraction. The distribution of Thy-1 antigen among the respective areas within the cerebrum was not significantly different, and it is suggested that Thy-1 antigen may be present evenly in the neuronal membranes of the cerebrum. Based on these results, Thy-1 antigen is considered to represent a useful marker of cerebral neuronal membranes, especially in the synaptic region, regardless of the kind of neurotransmitters.

Surface Proteins of Cultured Mouse Cerebellar Cells

Surface proteins of cultured monolayer cells from embryonic and early postnatal C57BL/6J mouse cerebella were identified by a lactoperoxidase-catalysed 131iodine labelling technique. Major iodinated polypeptides have molecular weights of approximately 200, 145, 120, 100, 85, 65, 50, and 30 x 10(3) (P200, P145,...) as estimated by sodium dodecylsulphate polyacrylamide gel electrophoresis. Membrane glycoproteins, of apparent molecular weights 200, 145, 100, 85, and 50 x 10(3), are detected by biosynthetic labelling with [3H]fucose. The two major iodinated proteins are the glycoproteins P200 and P145. P145 is released from the cells into the medium together with other surface proteins. No changes in the patterns of labelled cerebellar cell surface proteins are detectable between embryonic day 17 and postnatal day 10. A pattern similar to the one seen with cerebellum is obtained with embryonic day 12 and 17 cerebral cortex. Cultured retinal cells from 2-day-old mice, skin fibroblasts, and L-cells display a distinctly different pattern, which does not contain P145 as a major iodinated component. In granule cell-enriched fractions of cerebellar cells the two glycoproteins P200 and P145 are proportionately increased, while three proteins, P100, P85, and P50, are more abundant in the glial cell-enriched fraction. These three polypeptides are also enriched in cells obtained from staggerer mutant mice. An antiserum against 4-day-old cerebellar cells (anti-NS-4) precipitates the 145 and 200 x 10(3) molecular weight proteins, from lysates of both embryonic cerebral and postnatal cerebellar cells. From lysates of mouse retinal cells, anti-NS-4 antiserum precipitates two proteins with molecular weights of 140 and 210 x 10(3).

Isolation of glial cell-enriched and -depleted populations from mouse cerebellum by density gradient centrifugation and electronic cell sorting

Preparative amounts of populations enriched and depleted in glial cells have been isolated from 10-day-old mouse cerebella. Discontinuous density bovine serum albumin (BSA) gradients provide two distinct populations: the one derived from the 10-15% BSA interface is enriched in cyclic nucleotide phosphohydrolase (CNPase) activity, and a percentage of S-100, GFA protein, and NS-1 antigen-positive cells; the other, located as the 15-31% interface, contains a cell population depleted in these compounds. This report also describes the first use of flow microfluorimetry and electronic cell sorting techniques for the analysis and isolation of cell populations derived from the mammalian central nervous system. Glial cell-enriched and -depleted populations obtained by BSA density gradient centrifugation were analyzed for their forward angle light scattering properties and their capacity to bind anti-corpus anti-serum to the cell surface. The glial cell-enriched fraction shows a different frequency distribution of light scattering than the glial-depleted fraction. Anti-corpus callosum antiserum binds preferentially to the glial cell-rich fraction. Cells can be sorted into corpus callosum antigen-positive and -negative cell fractions and recovered with a viability of more than 95% as judged by trypan blue exclusion. Anti-corpus callosum-positive sorted cells are enriched in CNPase activity, S-100, and glial fibrillary acidic proteins.

Metabolic studies on ethanolamine phosphoglycerides in neuronal and glial cells.

Marked differences in phospholipid metabolism have been observed between glial and neuronal cell enriched fractions. Recently, evidence was obtained for a faster turnover of glycerophospholipids in neurons than in glial cells, since neurons contained a considerably higher phospholipase A1 and A2 activity when compared to the glial cell enriched fraction (Woelk et al., 1973). Furthermore the neuronal cell bodies were found to possess a much higher rate of exchange of both serine and ethanolamine into the phospholipids than the glial cell enriched fraction (Goracci et al., 1973) and Freysz et al., (1969), showed in their extensive investigation on the kinetics of the biosynthesis of phospholipids in neurons and glial cells, isolated from rat brain cortex, that neuronal phospholipids had a faster turnover than glial phospholipids. Recent results, presented by Woelk et al. (1974), indicated that phosphatidylinositol and phosphatidylcholine had the fastest and ethanolamine plasmalogen the slowest turnover in both cell populations.KeywordsGlial CellNeuronal Cell BodyFast TurnoverPreputial GlandDiacyl GlycerolThese keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Changes in some enzymic activities of separated neuronal and glial cell-enriched fractions from rat brains during development

Bulk-prepared neuronal perikarya and glial fractions have been used to study developmental changes of some enzymic activities concerning glycolysis and synthesis of neurotransmitters. Somewhat higher pyruvate kinase activity was found in neuronal perikarya than in glial cells, and its rapid rise was observed during early developmental stages. Increased K(+) concentration orD-glutamate addition to the incubation medium enhanced consumption of phosphoenolpyruvate. This activation of the enzyme was small just after birth, but it increased in parallel with development to adult level, where the activation in glial fractions was over twice that in neuronal fractions. Choline acetyltransferase activity was found in purified neuronal fractions and increased with age; glutamate decarboxylase was also found in high activity in purified neuronal fractions and increased with development. However, some enzymic activities were also found in glial fractions, and possibilities of contamination by synaptosomal, myelin, or other subfractions are discussed.

Preparation of glial plasma membrane from a cell fraction enriched in astrocytes

A technique for obtaining glial plasma membrane has been developed, starting with a bulk-prepared glial cell-enriched fraction from rabbit cerebral cortex. The astrocytic-enriched fraction was hand-homogenized in isotonic sucrose media, and the crude membrane fraction sedimented at 3,000g. The isolation of a membrane-enriched fraction was accomplished with sucrose density gradient centrifugation. The plasma membrane fraction was collected at the interphase between 31.5% and 25.5% sucrose. Enzymatic and electron-microscopical analyses indicated a 4-7-fold enrichment in plasma membrane, and a 15-20% contamination with microsomal and mitochondrial material. Some multilaminar membrane structures were also seen in the fraction.

Cellular and subcellular distribution of the S-100 protein in rabbit and rat central nervous system.

The cellular and subcellular distribution of the S-100 protein in rabbit and rat central nervous system was studied both quantitatively and qualitatively. Microcomplement fixation estimations on bulk-prepared neuronal and glial cells showed at least five to six times higher amounts of water-soluble S-100 in glial cell-enriched fractions as compared to fractions enriched in neuronal perikarya. Nerve cell fractions contained a higher percent of tissue-bound S-100 protein. High levels of S-100 protein were found in mitochondria and soluble protein fractions. Immunoelectron microscope investigations demonstrated S-100 protein in neuronal structures, such as the postsynaptic membrane and part of the plasma membrane. Among glial cells the astrocytic filaments contained high levels of S-100 protein. S-100 was also found in most subcellular membranes of astrocytes and oligodendrocytes.

Protein synthesis in neurons and glial cells by extrahepatic cholestasis in rats

Extrahepatic cholestasis was achieved by ligating the bile duct in rats. The incorporation of l-[4,5- 3H]leucine into the proteins of control and cholestatic brain slices was studied by incubation in a buffered salt medium. Neuronal and glial cell-enriched fractions were prepared by a sucrose-Ficoll gradient centrifugation method. Incorporation was decreased in brain slices from the cholestatic animals. This decrease was confined to the glial fraction. In a parallel series of experiments the brain radioactivity was measured 30 min after injecting l-[4,5- 3H]leucine intraperitoneally. Both trichloroacetic acid (TCA) soluble (reflecting free leucine) and precipitable (protein incorporated) leucine radioactivities were increased as well as the glial TCA-precipitable material. In opposite the neuronal fraction was decreased. Double-labeling experiments with l-[U- 14C]- and l-[4,5- 3H]-labeled leucine given intraperitoneally at different time points suggested slightly higher brain protein turnover during cholestasis. The results from in vitro and in vivo experiments were compared and discussed in relation to previous morphological material and biological studies.

Potassium accumulation by bulk prepared neuronal and glial cells.

Abstract— Neuronal and glial cell enriched fractions were prepared by density gradient centrifugation of suspensions from rabbit cerebral cortex. The two cell types were incubated separately in media of extracellular ionic composition. The potassium accumulation was determined from analysis of potassium content of the cells by ultramicro flame photometry. Both neuronal and glial cells were capable of active potassium transport which was inhibited by ouabain (2 × 10−4m). The glial cells could accumulate potassium up to four to five times the concentration of the incubation medium and neurons up to one and a half to two times the medium concentration. The respiration in low potassium media was stimulated 15 per cent for neurons and 85 per cent for glia when potassium was added to a final concentration of 50 mm. The uptake by both neurons and glia showed temperature and sodium dependence. There was a definite magnesium requirement for the potassium uptake, particularly demonstrable for glial cells. Calcium inhibited potassium uptake by glia but stimulated slightly that by neurons.

Amino acid incorporation in vitro into protein of neuronal and glial cell-enriched fractions.

Abstract—Slices of rabbit cerebral cortex were incubated in the presence of labelled amino acids. Following incubation, neuron‐ and gliaenriched fractions were obtained by density gradient centrifugation and the TCA‐insoluble radioactivity determined. The protein‐bound radioactivity was five to six times higher in the neuronal‐enriched fraction than in the glial‐enriched fraction after incubation with tritiated leucine. The neuronal fraction incorporated also a number of other amino acids to a higher extent than the glial fraction (neuron/glia ratio 2·5‐6). A definite dependence of incorporation on the rate of oxygenation was demonstrated. The suppression of amino acid incorporation was more marked for the neuronal fraction than for the glial fraction during incubation in relative hypoxia. An increase of potassium concentration in the incubation medium enhanced the amino acid incorporation in both fractions. Low sodium levels decreased the incorporation. Puromycin inhibited incorporation to approximately 30 per cent of control for both fractions. Addition of cycloheximide and dinitrophenol resulted in greater inhibition of incorporation in the neuronal fraction than in the neuroglial fraction. Actinomycin D did not markedly affect the incorporation in any fraction. These results are discussed in relation to in vivo and in in vitro differences for transport and incorporation of amino acids.