Inhibition of NADPH Oxidase Activation in Oligodendrocytes Reduces Cytotoxicity Following Trauma

Spinal cord injury is a debilitating neurological disorder that initiates a cascade of cellular events that result in a period of secondary damage that can last for months after the initial trauma. The ensuing outcome of these prolonged cellular perturbations is the induction of neuronal and glial cell death through excitotoxic mechanisms and subsequent free radical production. We have previously shown that astrocytes can directly induce oligodendrocyte death following trauma, but the mechanisms regulating this process within the oligodendrocyte remain unclear. Here we provide evidence demonstrating that astrocytes directly regulate oligodendrocyte death after trauma by inducing activation of NADPH oxidase within oligodendrocytes. Spinal cord injury resulted in a significant increase in oxidative damage which correlated with elevated expression of the gp91 phox subunit of the NADPH oxidase enzyme. Immunohistochemical analysis confirmed the presence of gp91 phox in oligodendrocytes in vitro and at 1 week following spinal cord injury. Exposure of oligodendrocytes to media from injured astrocytes resulted in an increase in oligodendrocyte NADPH oxidase activity. Inhibition of NADPH oxidase activation was sufficient to attenuate oligodendrocyte death in vitro and at 1 week following spinal cord injury, suggesting that excitotoxicity of oligodendrocytes after trauma is dependent on the intrinsic activation of the NADPH oxidase enzyme. Acute administration of the NADPH oxidase inhibitor apocynin and the alpha-amino-3-hydroxy-5-methylisoxazole-4-propionate channel blocker 2,3-dihydroxy-6-nitro-7-sulfamoyl-benzo[f]quinoxaline-2,3-dione significantly improved locomotor behavior and preserved descending axon fibers following spinal cord injury. These studies lead to a better understanding of oligodendrocyte death after trauma and identify potential therapeutic targets in disorders involving demyelination and oligodendrocyte death.     

The influence of life history traits on the phenological response of British butterflies to climate variability since the late‐19th century

Many species of plants and animals have advanced their phenology in response to climate warming in recent decades. Most of the evidence available for these shifts is based on data from the last few decades, a period coinciding with rapid climate warming. Baseline data is required to put these recent phenological changes in a long‐term context. We analysed the phenological response of 51 resident British butterfly species using data from 83 500 specimens in the collections of the Natural History Museum, London, covering the period 1880–1970. Our analysis shows that only three species significantly advanced their phenology between 1880 and 1970, probably reflecting the relatively small increase in spring temperature over this period. However, the phenology of all but one of the species we analysed showed phenological sensitivity to inter‐annual climate variability and a significant advancement in phenology in years in which spring or summer temperatures were warm and dry. The phenologies of butterfly species were more sensitive to weather if the butterfly species was early flying, southerly distributed, and a generalist in terms of larval diet. This observation is consistent with the hypothesis that species with greater niche breadth may be more phenologically sensitive than species with important niche constraints. Comparison of our results with post‐1976 data from the UK Butterfly Monitoring Scheme show that species flying early in the year had a greater rate of phenological advancement prior to the mid‐1970s. Additionally, prior to the mid‐1970s, phenology was influenced by temperatures in March or April, whereas since 1976, February temperature had a stronger influence on the phenology. These results suggest that early flying species may be approaching the limits of phenological advancement in response to recent climate warming.     

The pathology of embryo death caused by the male-killing Spiroplasma bacterium in Drosophila nebulosa

Background

Inherited bacteria that kill male offspring, male-killers, are known to be common in insects, but little is understood about the mechanisms used by male-killing bacteria to kill males. In this paper we describe the tempo and changes that occur during male-killing by Spiroplasma bacteria in the host Drosophila nebulosa.

Results

Spiroplasma infected D. nebulosa males were developmentally retarded from 6–8 h into embryonic development at 25°C, and arrested at between stages 12 and 13 of embryogenesis (10–12 h). Dying males were characterized by a failure to form segments, and ultimately disintegration of the normal oval embryonic shape. Prior to death, dying males exhibited widespread apoptosis, as testified by TUNEL staining.

Conclusion

The Spiroplasma kills male Drosophila in a narrow developmental period, shortly after the formation of the host dosage compensation complex that is required for male-killing. Male death is preceded by widespread apoptosis, but it is uncertain if this is primary or secondary apoptosis.     

Stock information requirements for quota management systems in commercial fisheries

Economic inefficiency and other problems associated with managing fisheries through restrictions on fishing times, places and gear have led to development of management systems based on individual fishers' quotas. But this shift from input controls to output controls calls for much more accurate and timely stock assessments. The risk of stock collapse resulting from overfishing, coupled with growing pressure for low-risk resource management policies, call for conservative quota-setting in the face of uncertain stock information. Under existing assessment systems, quotas may need to be so conservative that foregone catches could wipe out the economic gains from quota management. This problem might be overcome by taking advantage of the incentives of quota-holders to contribute to, and invest in, the gathering of information to improve stock assessments.     

Lunar synchronization of the monthly reproductive rhythm in the sea urchin Centrostephanus coronatus Verrill

The monthly reproductive rhythm in the diadematid sea urchin Centrostephanus coronatus Verrill at Santa Catalina Island, California, was studied in the summer of 1973 and the results are compared with data for the summer of 1969. In the summer of 1973 the more extreme spring tides coincided with the new moon, while in the summer of 1969 the more extreme spring tides coincided with the full moon. The reproductive rhythm in both years was closely synchronized with lunar phases and not with the monthly tidal cycles; spawning occurred near the third lunar quarter in both years. These observations suggest that this monthly reproductive rhythm is synchronized by monthly changes in moonlight, and not by monthly tidal changes.     

On the structural and functional components of coated vesicles.

Despite the diversity of their known functions, coated vesicles from different tissues contain a rather similar spectrum of proteins, in addition to their major coat protein, clathrin. In particular, each coated vesicle preparation shows a doublet of polypeptide species, on sodium dodecyl sulphate-containing gel electrophoresis, of apparent molecular weight in the region 30,000 to 36,000. Using bullock brain as a source, these molecules are found in association with possible trimers or higher multiples of clathrin, obtained by dissolving coated vesicles in cholate. They may play a structural role relating to the vertices or edges of the lattices of pentagons and hexagons of the polyhedral coats.Purified coated vesicles (e.g. from chicken oocytes) seem to contain relatively small amounts of specific proteins in terms of “contents”. This suggests that the bulk of the isolated particles, especially those in the small size range (500 to 800 Å diam.), may be “empty” of contents, although many still retain a lipid vesicle. These empty structures could represent a pool of recycling coated vesicle components formed after release (possibly from larger vesicles (800 to 1500 Å diam.)) of the specific contents, at their particular destination.     

Cytochemical identification of human and murine pituitary corticotrophs and somatotrophs as APUD cells

Summary Cytochemical techniques, performed sequentially on single sections, have confirmed the identity of human and murine pituitary corticotrophs as APUD cells. These same methods indicate that in both species the acidophil somatotroph, identified as such by immunofluorescence using anti-human GH, possesses APUD qualities not only with respect to amine-handling, but also in terms of enzyme content.Inclusion of the somatotroph in the APUD series of cells which produce polypeptide hormones has far-reaching implications.