High mobility group box 1 (HMGB1) and anti-HMGB1 antibodies and their relation to disease characteristics in systemic lupus erythematosus

Introduction  

High Mobility Group Box 1 (HMGB1) is a nuclear non-histone protein. HMGB1, which is secreted by inflammatory cells and passively released from apoptotic and necrotic cells, may act as a pro-inflammatory mediator. As apoptotic cells accumulate in systemic lupus erythematosus (SLE), HMGB1 levels might be increased in SLE. HMGB1 may also serve as an autoantigen, leading to the production of anti-HMGB1 antibodies. In this study we determined levels of HMGB1 and anti-HMGB1 in SLE patients in comparison to healthy controls (HC) and analysed their relation with disease activity.     

Contribution of fungal biomass to the diet of a freshwater isopod (Lirceus sp.)

SUMMARY. 1. The direct contribution of fungal biomass to the carbon needs of a freshwater isopod (Lirceus sp.) was measured using 14C-labelled fungi on leaf material. 14C-glucose was added to fungus-inoculated leaf discs periodically throughout the growth of the fungus. Amount of label incorporated into fungal biomass, radioactivity appearing in Lirceus after feeding on labeled fungus and the standing stock of fungus were used to calculate incorporation of fungal C by the consumer.
2. Incorporation rates ranged from 0.06 to 70 ng fungal C mg wet wt isopod-1h-1. These rates of incorporation represent from 0.05 to 57% of C respired by the isopod.
3. Fungal C does not meet the carbon needs of this consumer and the role of fungi as modifiers of the leaf substrate may be more significant than their role as a food source.     

Fisher Survival in Eastern Ontario

Abstract: Fishers (Martes pennanti) have recolonized eastern Ontario, Canada, but little is known about the survival of this harvested population. We estimated fisher survival and cause-specific mortality in Leeds and Grenville County, Ontario, from 2003–2005. The overall 2-year survival rate (95% CI) was 0.35 (0.21-0.56, n = 59). We attributed observed mortality rates mainly to natural causes (28.6%) and nuisance trapping (21.4%). Given reported recruitment rates, our estimated fisher mortality has likely led to population declines in the study area, especially during 2003. Thus, we do not recommend an increase in fisher harvest quotas in the study area at this time.     

Direct Effects of Ca2+-Channel Blockers on Plasma Membrane Cation Channels of Amaranthus tricolor Protoplasts

Ca²⁺-channel blockers at concentrations greater than 1 mmolm^–3, directly affect the activity of K ⁺selective channelsin the plasma membrane of Amaranthus tricolor protoplasts. Theseeffects are not mediated by the blockade of Ca²⁺ channels. Blockers tested included 1, 4-dihydropyridines (nifedipine,nicardipine), verapamil, bepridil, Gd³⁺ and La³⁺, applied towhole-cell and detached outside-out patches of plasma membraneat concentrations from 50µmol m^–3 to 100 mmol m^–3.For certain experiments the concentration of Ca²⁺ on the cytoplasmicside of the plasma membrane ([Ca²⁺]cyt) was buffered at either50ftmol m^–3 or 500 µmol m^–3. The principal currents observed in whole-cells flowed throughcation outward rectifier (OR) channels. Each blocker causedan immediate reduction of time-dependent outward currents atdoses down to 1 mmol m^–3 and produced a different, reversible,kinetic block of the outward current, independent of the levelof [Ca²⁺]cyt. Verapamil also activated a sustained inward cationcurrent at negative p.d. The same effects were found with individualchannels in detached outside-out patches. Conductance and selectivityof the cation OR channels were unchanged by the drugs. [Ca²⁺]ex, was varied over a range from 0 to 10 mol m^–3.Progressively lower [Ca²⁺]eI, increasingly enhanced the maximumamplitude of the time-dependent currents. Time-constants fordecay of inward tail currents were increased at low [Ca²⁺]eit.These effects were rapidly reversible. Although there was noevidence that the cation ORs in plasma membrane of Amaranthustricolor were dependent on [Ca²⁺]cyl for their activation, theywere sensitive to the concentration of free Ca²⁺ in the extracellularmedium. Key words: Verapamil, blocker, cation channels, Amaranthus, protoplasts     

Solute Accumulation by Grape Pericarp Cells: IV. PERFUSION OF PERICARP APOPLAST VIA THE PEDICEL AND EVIDENCE FOR XYLEM MALFUNCTION IN RIPENING BERRIES

Findlay, N., Oliver, K. J., Nii, N. and Coombe, B. G. 1987.Solute accumulation by grape pericarp cells. IV. Perfusion ofpericarp apoplast via the pedicel and evidence for xylem malfunctionin ripening berries.—J. exp. Bot. 38: 668–679. ¹⁴C-labelled sucrose was applied to freshly-cut pedicels ofexcised unripe and ripening grape berries and let perfuse fordifferent periods; skin and flesh tissues were then extractedand the radioactivity partitioned and measured. Accumulationof radioactivity in a compartmented fraction was greatest inthe skin of unripe berries at the stage when sugar accumulationin vivo was slow. Total radioactivity of parts of berries showedthat activity spread rapidly throughout when the berry was unripebut slowed once ripening commenced. The perfusion of eosin from pedicels was also rapid in unripeberries but in ripe berries it was blocked beyond the pedicelat the outer edge of the 'brush' where the pericarp is aerenchymatousand tanniniferous. The failure of movement through the vascularbundles beyond the brush could not be associated with the developmentof tyloses in tracheary elements; it appeared to be associatedwith stretched tracheids in the network of dorsal vascular bundlesevidenced by irregularities in the spacing of wall thickeningsand breaks in the bounding membranes. This physical disruptionof the tracheary elements of the vascular bundles occurred whenthe berry expands suddenly, about a week after the inceptionof rapid sugar accumulation. The different rates of perfusion limit the utility of the pedicelroute for studies of compartmentation and metabolism in grapeberries at different developmental stages. Nevertheless, therapid compartmentation of radioactivity after pedicel perfusionof unripe skin with ^l4C-labelled sucrose discounts the hypothesisthat the slow rate in skin in situ is due to an apoplastic inhibitor. Key words: Grape berry, accumulation, xylem malfunction