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41.
Rika Morishita Shinsuke Saga Noriko Kawamura †Yoshio Hashizume ‡Toshiaki Inagaki Kanefusa Kato Tomiko Asano 《Journal of neurochemistry》1997,68(2):820-827
Abstract: The localization of two forms of the γ subunit of G proteins, γ3 and γ12, was examined in the mammalian brain. Concentrations of these two γ subunits increased markedly, as did those of glial fibrillary acidic protein, during postnatal development in the rat cerebral cortex. In aged human brains, by contrast, the concentration of γ3 tended to decrease with age, whereas that of γ12 in the temporal cortex increased slightly. An immunohistochemical study of human brains revealed that γ3 was abundant in the neuropil, whereas γ12 was localized in glial cells. In the hippocampal formation of aged human brains, levels of γ12-positive cells, as well as levels of glial fibrillary acidic protein- and vimentin-positive astrocytes, increased, in particular in the CA1 subfield and the prosubiculum, in which there was a decrease in the number of pyramidal cells. The appearance of γ12-positive cells associated with the loss of pyramidal cells was also observed in the hippocampus of rats that had been treated with kainic acid. These results indicate that γ12 is strongly expressed in reactive astrocytes. In a study of cultured neural cells, we found that γ12 was predominant in glioma cells, such as C6 and GA-1 cells, in contrast with the specific localization of γ3 in PC12 pheochromocytoma cells, which are neuron-like cells. Taken together, the results indicate that γ3 and γ12 are selectively expressed in neuronal and glial cells, respectively, and that concentrations of γ3 and γ12 in the brain are related to the numbers and/or extent of maturation of these cells. 相似文献
42.
Bjørnar Hassel Niels Westergaard Arne Schousboe Frode Fonnum 《Neurochemical research》1995,20(4):413-420
Astrocytes and neurons cultured from mouse cerebellum and cerebral cortex were analyzed with respect to content and synthesis of amino acids as well as export of metabolites to the culture medium and the response to fluorocitrate, an, inhibitor of aconitase. The intracellular levels of amino acids were similar in the two astrocytic populations. The release of citrate, lactate and glutamine, however, was markedly higher from cerebellar than from cortical astrocytes. Neurons contained higher levels of glutamate, aspartate and GABA than astrocytic cultures. Cortical neurons were especially high in GABA and aspartate, and the level of aspartate increased specifically when the extracellular level of glutamine was elevated. Fluorocitrate inhibited the TCA cycle in the astrocytes, but was less effective in cerebellar neurons. Whereas neurons responded to fluorocitrate with an increase in the formation of lactate, reflecting, glycolysis, astrocytes decreased the formation of lactate in the presence of fluorocitrate, indicating that astrocytes to a high degree synthesize pyruvate and hence lactate from TCA cycle intermediates. 相似文献
43.
Astrocytes are the primary site of glutamate conversion to glutamine in the brain. We examined the effects of treatment with either dibutyryl cyclic AMP and/or the synthetic glucocorticoid dexamethasone on glutamine synthetase enzyme activity and steady-state mRNA levels in cultured neonatal rat astrocytes. Treatment of cultures with dibutyryl cyclic AMP alone (0.25 mM–1.0 mM) increased glutamine synthetase activity and steady state mRNA levels in a dose-dependent manner. Similarly, treatment with dexamethasone alone (10–7–10–5 M) increased glutamine synthetase mRNA levels and enzyme activity. When astrocytes were treated with both effectors, additive increases in glutamine synthetase activity and mRNA were obtained. However, the additive effects were observed only when the effect of dibutyryl cyclic AMP alone was not maximal. These findings suggest that the actions of these effectors are mediated at the level of mRNA accumulation. The induction of glutamine synthetase mRNA by dibutyryl cyclic AMP was dependent on protein synthesis while the dexamethasone effect was not. Glucocorticoids and cyclic AMP are known to exert their effects on gene expression by different molecular mechanisms. Possible crosstalk between these effector pathways may occur in regulation of astrocyte glutamine synthetase expression.Abbreviations used GS
glutamine synthetase
- dbcAMP
dibutyryl cyclic AMP
- MEM
minimal essential medium
- cyx
cycloheximide
- GRE
glucocorticoid response element
- CRE
cyclic AMP response element 相似文献
44.
Thompson R. C. A., Houghton A. and Zaman V. 1982. A study of the microtriches of adult Echinococcus granulosus by scanning electron microscopy. International Journal for Parasitology12: 579–583. The microtriches in different regions of the scolex and strobila of sexually mature Echinococcus granulosus were examined using the scanning electron microscope. E. granulosus was found to possess two morphologically distinct types of microthrix. A cylindrical, slender filamentous type of microthrix which appeared to be flexible was restricted to the scolex. On the strobila, the only type of microthrix observed was a flattened blade-like form which appeared to be rigid for most of its length. The occurrence of two distinct types of microthrix in separate regions of the body of E. granulosus suggests that they may be involved in different functional activities. 相似文献
45.
Callosobruchus maculatus (F.) is a tropical insect (Coleoptera: Bruchidae) that develops in Vigna unguiculata (Walp) seeds. In this beetle, there are two distinct adult forms that differ in their morphology, physiology and behaviour, the flight form and the flightless form. The development of C. maculatus is analyzed in a traditional store in Niger. During the dry season, 6 to 7 generations of the flightless form develop in the store. When the atmospheric water content increases during the rainy season, adults of the flight form appear and escape from the store. Experimental studies have shown that the adult polymorphism is induced during post-embryonic development and depends on prevailing abiotic factors during this period. The proportion of flight from adults is high when larvae develop in moist seeds (14–15% of water content). Under dry conditions (6–7% of water content) only flightless adult forms emerge from the seeds. Temperatures during development also influence adult polymorphism. In thermoperiodic conditions with 12–13% seed water content, the proportion of flight from adults increases with increasing duration of the thermophase. However, at low temperatures, a high proportion of flightless adult forms emerge, regardless of seed water content. The adaptive importance of these two abiotic factors on polymorphism induction is examined in this study.
Résumé Callosobruchus maculatus (F.) est un Coléoptère Bruchidae tropical qui se développe aux dépens des graines de Vigna unguiculata. Les adultes présentent un polymorphisme; il y a en effet deux formes, la forme voilière et la forme non voilière, distinctes par des critères morphologiques, physiologiques et comportementaux. L'évolution des populations de C. maculatus a été suivie pendant toute la saison sèche et le début de la saison des pluies dans la région de Niamey au Niger (13° LN) à l'intérieur d'un grenier traditionnel. Pendant toute la saison sèche, 6 à 7 générations de C. maculatus de la forme non voilière se succèdent à l'intérieur du grenier. Les adultes de la forme voilière, très actifs, apparaissent surtout au cours de la saison des pluies lorsque la teneur en eau de l'atmosphère et la teneur en eau des graines augmentent. Les études expérimentales réalisées au laboratoire montrent que le polymorphisme imaginal est induit au cours du développement post-embryonnaire et dépend des conditions climatiques dans lesquelles celui-ci a lieu. Le taux d'adultes de la forme voilière est élevé lorsque les larves se développent dans des graines à forte teneur en eau (14 ou 15%). Lorsque la teneur en eau des graines est faible (6 à 7%), il n'y a émergence que d'adultes de la forme non voilière. Lorsque la teneur en eau des graines est comprise entre 12 et 13%, le taux d'adultes de la forme voilière s'accroit et varie avec la durée de la thermophase. A basse température il y a toujours émergence d'adultes de la forme non voilière, quelle que soit la teneur en eau des graines. L'influence de ces deux facteurs abiotiques sur l'induction du polymorphisme imaginal joue probablement un rôle important dans les mécanismes adaptatifs permettant le maintien de cette espèce en zone tropicale.相似文献
46.
Jean C. Delumeau François Petitet Jocelyne Cordier Jacques Glowinski Joël Prémont 《Journal of neurochemistry》1991,57(6):2026-2035
The effects on cytosolic Ca2+ concentration of 2-chloroadenosine and [L-Pro9]-substance P, a selective agonist of NK1 receptors, were investigated on astrocytes from embryonic mice in primary culture. Cells responded to [L-Pro9]-substance P with a transitory increase in cytosolic Ca2+ which was of shorter duration when external Ca2+ was removed. A transient response to 2-chloroadenosine alone occurred. When simultaneously applied, [L-Pro9]-substance P and 2-chloroadenosine evoked a prolonged elevation of cytosolic Ca2+ (up to 30 min). This phenomenon was dependent on the presence of extracellular Ca2+, but insensitive to dihydropyridines, La3+, and Co2+, excluding the implication of voltage-operated Ca2+ channels. Arachidonic acid also induced a sustained elevation of cytosolic Ca2+, but did not increase further the response evoked by [L-Pro9]-substance P and 2-chloroadenosine. The activation of protein kinase C by a diacylglycerol analogue mimicked the effect of [L-Pro9]-substance P in potentiating the 2-chloroadenosine-evoked response. Like 2-chloroadenosine, pinacidil, which hyperpolarizes the cells by opening K+ channels, prolonged the elevation of cytosolic Ca2+ concentration induced by [L-Pro9]-substance P. Conversely, depolarization with 50 mM KCl canceled the effects of either pinacidil or 2-chloroadenosine applied with [L-Pro9]-substance P. Pertussis toxin pretreatment suppressed all the effects induced by 2-chloroadenosine. 相似文献
47.
Inhibitors of Urokinase and Thrombin in Cultured Neural Cells 总被引:2,自引:1,他引:1
Steven L. Wagner Alice L. Lau Ann Nguyen Jun Mimuro David J. Loskutoff Paul J. Isackson† Dennis D. Cunningham 《Journal of neurochemistry》1991,56(1):234-242
Recent studies have suggested important roles for certain proteases and protease inhibitors in the growth and development of the CNS. In the present studies, inhibitors of urokinase or thrombin in cultured neural cells and serum-free medium from the cells were identified by screening for components that formed sodium dodecyl sulfate-stable complexes with 125I-urokinase or 125I-thrombin. Rinsed glioblastoma possessed two components that complexed 125I-urokinase. One was type 1 plasminogen activator inhibitor (PAI-1), because the 125I-urokinase-containing complexes were immunoprecipitated with anti-PAI-1 antibodies. The other component formed complexes with 125I-urokinase that were not recognized by antibodies to PAI-1 or protease nexin-1 (PN-1). Its identity is unknown. In addition to these cell-bound components, the glioblastoma cells also secreted two inhibitors that formed complexes with 125I-urokinase; one was PAI-1, and the other was PN-1. The secreted PN-1 also formed complexes with 125I-thrombin. It was the only thrombin inhibitor detected in these studies. Human neuroblastoma cells did not contain components that formed detectable complexes with either 125I-urokinase or 125I-thrombin. However, human neuroblastoma cells did contain very low levels of PN-1 mRNA and PN-1 protein. Added PN-1 bound to the surface of both glioblastoma and neuroblastoma cells. This interaction accelerated the inhibition of thrombin by PN-1 and blocked the ability of PN-1 to form complexes with 125I-urokinase. Thus, cell-bound PN-1 was a specific thrombin inhibitor.(ABSTRACT TRUNCATED AT 250 WORDS) 相似文献
48.
C. Guarnieri G. Zucchelli F. Bernardi M. Scheda A. F. Valentini M. Calandriello 《Free radical research》1991,15(1):11-16
In the gingival crevicular fluid (GCF) of control and chronic adult periodontitis (CAP) patients there is a spontaneous release of O2- radicals from polymorphonuclear leukocytes (PMN). The addition of the exogenous stimuli phorbol myrystate acetate (PMA) decreased the O2- formation in control GCF, while in CAP patients produced a marked enhancement of O2- generation.
The circulating PMN of control subjects did not show a spontaneous O2- formation, differently from CAP patients. On the contrary, a similar O2- production was measured when the circulating PMN were stimulated with PMA.
Moreover, the antioxidant activity measured in 10μl of cell free gingival supernatant (GS) of control and CAP patients had the same values by inhibiting 12.6% and 18.9% respectively of the O2- formation supported by a xanthine/xanthine oxidase system.
Probably, the protective or destructive effect of PMN in GCF of CAP patients depends on the variations of the rate of O2- formation in respect to the intrinsic antioxidant property of GS. 相似文献
The circulating PMN of control subjects did not show a spontaneous O2- formation, differently from CAP patients. On the contrary, a similar O2- production was measured when the circulating PMN were stimulated with PMA.
Moreover, the antioxidant activity measured in 10μl of cell free gingival supernatant (GS) of control and CAP patients had the same values by inhibiting 12.6% and 18.9% respectively of the O2- formation supported by a xanthine/xanthine oxidase system.
Probably, the protective or destructive effect of PMN in GCF of CAP patients depends on the variations of the rate of O2- formation in respect to the intrinsic antioxidant property of GS. 相似文献
49.
Herbert M. Geller Vanya Qui;ones-Jenab Maciej Poltorak William J. Freed 《Journal of cellular biochemistry》1991,45(3):279-283
Immortalized cell lines can serve as model systems for studies of neuronal development and restoration of function in models of neurological disease. Cell lines which result from spontaneous or experimentally-induced tumors have been used for these purposes. More recently, the techniques of genetic engineering have resulted in the production of cell lines with specific desired characteristics. This has been accomplished by insertion of a desired gene into a pre-existing immortal cell or by immortalizing primary cells. The production of immortal cell lines using temperature-sensitive immortalizing genes offers an additional method of controlling gene expression, and thereby controlling cell proliferation and differentiation. In the nervous system, these techniques have produced immortal cell lines with neuronal and glial properties. 相似文献
50.
Michel P. Rathbone Pamela J. Middlemiss John W. Gysbers Susan DeForge Penny Costello Rolando F. Del Maestro 《In vitro cellular & developmental biology. Animal》1992,28(7-8):529-536
Summary Presumptive astrocytes isolated from 10-day white Leghorn chick embryos, Factor VIII-positive human brain capillary endothelial
cells, meningeal fibroblasts from 10-day chick embryos, Swiss mouse 3T3 cells, and human astrocytoma cell lines, SKMG-1 and
U373, were rendered quiescent when placed in culture medium that contained 0 or 0.2% serum for 48 h; their proliferation was
markedly reduced and they incorporated [3H]thymidine at a low rate. [3H]Thymidine incorporation and cell proliferation were induced in all types of cells by addition of guanosine, GMP, GDP, GTP,
and to a lesser extent, adenosine, AMP, ADP or ATP to the culture medium. The stimulation of proliferation by adenosine and
guanosine was abolished by 1,3-dipropyl-7-methylxanthine (DPMX), an adenosine A2 receptor antagonist, but not by 1,3,-dipropyl-8-(2-amino-4-chorophenyl)xanthine (PACPX), an A1 antagonist. Stimulation of proliferation by the nucleotides was not abolished by either DPMX or PACPX. The P2 receptor agonists,α,β-methyleneATP and 2-methylthioATP, also stimulated [3H]thymidine incorporation into the cells with peak activity at approximately 3.5 and 0.03 nM, respectively. These data imply that adenosine and guanosine stimulate proliferation of these cell types through activation
of an adenosine A2 receptor, and the stimulation of cell proliferation by the nucleotides may be due to the activation of purinergic P2y receptors. As the primary cultures grew older their growth rate slowed. The capacity of the purine nucleosides and nucleotides
to stimulate their growth diminished concomitantly. The 3T3 cells showed neither decreased growth with increased passages
nor reduced response to the purines. In contrast, although the doubling time of the immortalized human astrocytoma cell lines
SKMG-1 and U373 remained constant, the responsiveness to purinergic stimulation of the U373 cells decreased but that of the
SKMG-1 did not. These data are compatible with a decrease in the number, or the ligand-binding affinity of the purinergic
receptors, or a decreased coupling of purinergic receptors to intracellular mediators in primary cells aged in tissue culture. 相似文献