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31.
Mark T Uhlik Amy N Abell Bruce D Cuevas Kazuhiro Nakamura Gary L Johnson 《Biochimie et biologie cellulaire》2004,82(6):658-663
Mitogen-activated protein kinase (MAPK) pathways are activated by a plethora of stimuli. The literature is filled with papers describing the activation of different MAPKs by almost any stimulus or insult imaginable to cells. In this review, we use signal transduction wiring diagrams to illustrate putative upstream regulators for the MAPK kinase kinases, MEKK1, 2, and 3. Targeted gene disruption of MEKK1, 2, or 3 defined phenotypes for each MEKK associated with loss of specific MAPK regulation. Genetic analysis of MEKK function clearly defines specific components of the wiring diagram that require MEKK1, 2, or 3 for physiological responses. We propose that signal transduction network wiring diagrams are valuable tools for hypothesis building and filtering physiologically relevant phenotypic responses from less connected protein relations in the regulation of MAPK pathways. 相似文献
32.
Agneta Oskarsson Katherine S. Squibb Bruce A. Fowler 《Biochemical and biophysical research communications》1982,104(1):290-298
Gel chromatography of kidney postmitochondrial fractions from control rats 2 hr after injection of 203Pb or after in vitro incubation with 203Pb disclosed the presence of two fractionated Pb-binding components plus binding in the void volume and total volume regions. The binding of Pb to the two components, with molecular weights of 11,500 and 63,000 daltons, was markedly decreased in Pb-pretreated rats. Sodium dodecyl sulfate-gel electrophoresis and autoradiography showed the presence of one major 203Pb band with an estimated molecular weight of 60,000 daltons. The 11,500-dalton peak did not incorporate 14C-leucine nor did concomitant administration of cycloheximide with the 203Pb inhibit incorporation of 203Pb activity, suggesting that the component is a preformed constituent of the kidney. In vitro incubation of brain, liver and lung postmitochondrial supernatants with 203Pb disclosed that these two binding components were also present in brain but not in liver or lung, suggesting a target tissue-specific localization for these Pb-binding macromolecules. 相似文献
33.
Forearm skin of Stage XXIV Rana pipiens, which cannot regenerate limbs, was removed and placed upon the skinned forearms of young axolotls. The axolotl limbs were amputated immediately through the level of the grafts. Frog epidermis migrated to cover the amputation surface. Dedifferentiation and early blastema formation occurred beneath the frog wound epidermis. Limb regeneration continued, but in time axolotl epidermis overgrew the frog epidermis. The experiment shows that epidermis from nonregenerating frog limbs is still capable of supporting typical epimorphic regeneration. 相似文献
34.
35.
Nitrous Oxide Production by Organisms Other than Nitrifiers or Denitrifiers 总被引:17,自引:12,他引:5 下载免费PDF全文
Heterotrophic bacteria, yeasts, fungi, plants, and animal breath were investigated as possible sources of N2O. Microbes found to produce N2O from NO3− but not consume it were: (i) all of the nitrate-respiring bacteria examined, including strains of Escherichia, Serratia, Klebsiella, Enterobacter, Erwinia, and Bacillus; (ii) one of the assimilatory nitrate-reducing bacteria examined, Azotobacter vinelandii, but not Azotobacter macrocytogenes or Acinetobacter sp.; and (iii) some but not all of the assimilatory nitrate-reducing yeasts and fungi, including strains of Hansenula, Rhodotorula, Aspergillus, Alternaria, and Fusarium. The NO3−-reducing obligate anaerobe Clostridium KDHS2 did not produce N2O. Production of N2O occurred only in stationary phase. The nitrate-respiring bacteria produced much more N2O than the other organisms, with yields of N2O ranging from 3 to 36% of 3.5 mM NO3−. Production of N2O was apparently not regulated by ammonium and was not restricted to aerobic or anaerobic conditions. Plants do not appear to produce N2O, although N2O was found to arise from some damaged plant tops, probably due to microbial growth. Concentrations of N2O above the ambient level in the atmosphere were found in human breath and appeared to increase after a meal of high-nitrate food. 相似文献
36.
Evidence for Glucocorticoid Target Cells in the Rat Optic Nerve. Hormone Binding and Glycerolphosphate Dehydrogenase Induction 总被引:1,自引:1,他引:0
Jerrold S. Meyer Paula J. Leveille Jean de Vellis John L. Gerlach Bruce S. McEwen 《Journal of neurochemistry》1982,39(2):423-434
Abstract: Biochemical evidence suggests that neuroglia are responsive to glucocorticoids, yet previous studies of glucocorticoid localization have typically failed to demonstrate significant uptake by neuroglial cells. To further investigate this problem, we measured glycerol-3-phosphate dehydrogenase (GPDH) activity and glucocorticoid receptor binding capacity in normal rat optic nerves and in those undergoing Wallerian (axonal) degeneration. Binding studies were also performed on hippocampus and anterior pituitary for comparison purposes. Normal optic nerve preparations possessed a high level of GPDH activity that was glucocorticoid-inducible and that increased further following axonal degeneration. Antibody inactivation experiments demonstrated the presence of more enzyme molecules in the degenerating nerve preparations. Correlative immunocytochemical studies found GPDH-positive reaction product only in morphologically identified oligodendrocytes, a result that is consistent with the previously reported localization of this enzyme in rat brain. Optic nerve cytosol fractions displayed substantial high-affinity binding of both dexamethasone (DEX) and corticosterone (CORT) that, like GPDH, was elevated approximately twofold in degenerating nerves. Finally, in vivo accumulation of [3 H]DEX and [3 H]CORT by optic nerve and other myelinated tracts was examined using nuclear isolation and autoradiographic methods. Although neither steroid was found to be heavily concentrated by these tissues in vivo , a small preference for DEX was observed in the nuclear uptake experiments. These results are discussed in terms of the hypothesis that glial cells are targets for glucocorticoid hormones. 相似文献
37.
Charles M. Paden Bruce S. McEwen Jack Fishman Lenore Snyder Valerie DeGroff 《Journal of neurochemistry》1982,39(2):512-520
Abstract: We have examined the ability of various steroids to compete for high-affinity binding of 3H-labeled ligands to catecholamine receptors in membranes prepared from rat cerebral cortex, striatum, and anterior pituitary. Ligands employed were: [3H]WB4101, [3H]prazosin, [3H]yohimbine, and [3H]clonidine (alpha-noradrenergic); [3H]dihydroalprenolol (beta-noradrenergic); [3H]spiperone and [3H]ADTN (dopaminergic). Only the 17β estrogens were effective and only binding of [3H]spiperone and [3H]ADTN in striatum and [3H]WB4101 and [3H]prazosin in cerebral cortex was reduced. Thus putative dopaminergic and alpha1-noradrenergic sites alone appear to recognize estrogens. A slight competitive effect on [3H]spiperone binding to anterior pituitary membranes was also observed. Among the 17β estrogens tested, the most effective in all cases was the catechol estrogen 2-hydroxyestradiol (2-OHE2). The ability of 2-OHE2 (IC50= 20–30 μM) to inhibit ligand binding to alpha1 receptors was comparable to that of norepinephrine (IC50= 10–20 μM), whereas for dopamine receptors in striatum and pituitary 2-OHE2 was an order of magnitude less effective than dopamine (IC30= 12 μM) in reducing binding of 3H ligands. Estradiol-17β and 2-hydroxyestrone were also able to inhibit binding, but the order of steroid potency was different for alpha1 and dopaminergic receptors. Progesterone, testosterone, and corticosterone were without effect in all cases. These results show that there is specificity of steroid interactions with catecholamine receptors in the brain, both in terms of steroid structure and receptor type. The possible relevance of these interactions to neuroendocrine function is discussed. 相似文献
38.
Bruce Griffing 《Journal of theoretical biology》1982,95(1):181-198
This paper and the next member of the series, deal with genetical mechanisms responsible for the evolution of eusociality (a level of social organization that includes differentiated sterile castes) among the “social” insects. Eusociality has evolved in a number of different species. Two different types of genetic systems are represented among these species: diplodiploidy (both sexes diploid) and haplodiploidy (haploid males and diploid females). The present paper examines the evolution of a sterile caste system in the context of diplodiploidy, and the next paper considers the evolution of eusociality in the context of haplodiploidy.The present study demonstrates that if the sterile diploid caste members are related to the reproductive members of the group, eusociality can evolve. This is true because the caste associate gene effects are included in the function determining gene frequency change (i.e. Δpi). Also, since the caste gene effects are expressed only through the associate dimension of gene activity, they can cause morphological and behavioral adaptations to occur which are peculiar to the caste members, and need not be expressed in the reproducing members of the group. Thus caste differentiation is possible. 相似文献
39.
Bruce Griffing 《Journal of theoretical biology》1982,94(4):951-966
A previous study, (V), in this series dealt with the problem of interaction among individuals in a population by utilizing a conceptual life-history model that assumed the synchronization of fitness components (viability and fecundity) for members within groups of interacting individuals. The model also assumed that the group members were not differentiated in any way. It was shown that these assumptions of synchronization and homogeneity of group members resulted in overall symmetric fitness values, and that selection operating on these symmetric values produced optimum short- and long-term results.Since the idealized model of paper (V) yields optimum selection results, it is of interest to consider specific biological mechanisms which can be used to fulfill the conceptual assumptions involved. The solution adopted in this study is to, first, require survival to occur at the group level. This forces the viability parameters to be identical for all group members.Second, the group composition is restricted to a single pair mating. This forces the fecundity parameters to be identical for members (sire and dam) of the same group. However, this solution causes a complication. Since each individual is identified as belonging to one of the two sexual types, it is necessary to extend the previous analysis in paper (V), to accommodate differentiated group members. It is shown that this differentiation leads to a non-symmetric fitness matrix. However, it is further shown that the selection results can be obtained by use of a ‘combined’ fitness matrix that is symmetric. Therefore, the important result is demonstrated that selection involving differentiated sire-dam groups possesses all of the optimum short- and long-term properties inherent in the original non-differentiated selection procedure developed in paper (V). It is speculated that these results could be of some significance with regard to the evolution of a monogamous, pair-bonding family structure. 相似文献
40.
Abstract: The opioid peptides Met- and Leu-enkephalin, dynorphin (1-13), and β-endorphin and the narcotic analgesics, morphine, levorphanol, and dextrorphan all produced a dose-dependent inhibition of nicotine (5 × 10?6m )-mediated release of [3H]norepinephrine ([3H]NE) from bovine adrenal chromaffin cells in culture. None of these agents affected [3H]NE release induced by high K+ (56 mm ). Although the above results suggest that the opioid peptides and narcotic analgesics inhibit catecholamine release from adrenal chromaffin cells in culture, we suggest that these effects are not mediated by specific opiate binding sites, since (1) the inhibition was only produced with high concentrations of the agents—the threshold concentrations were 10?7 to 10?5m and higher; (2) the inhibition produced by the narcotic analgesics did not display stereospecificity, because the (d-isomer, dextrorphan, was slightly more active than the l-isomer, levorphanol; (3) the narcotic antagonists naloxone, naltrexone, and levallorphan did not reverse the inhibition produced by either the narcotic analgesics (e.g., morphine) or the opioid peptides (e.g., dynorphin). These three antagonists themselves inhibited the nicotine-mediated release of [3H]NE from the adrenal chromaffin cells in culture. Finally (4), the I2-Tyr1 substituted analogues of β-endorphin and dynorphin that are biologically less active than the parent compounds produced an inhibition of the nicotine-mediated [3H]NE release similar to that of their parent compounds. These results do not support the idea that high-affinity stereospecific opiate binding sites are involved in the inhibitory modulation of nicotinic evoked catecholamine release from bovine adrenal chromaffin cells in culture. 相似文献