Energy-dependent contraction of swollen mitochondria: activation by nigericin.

The rate, extent, and efficiency of the energy-dependent contraction of heart mitochondria swollen in Na+ or K+ nitrate are all strongly activated by nigericin, an antibiotic which is known to support cation/H+ exchange in natural and model membranes. In the absence of nigericin, the cation selectivity sequence of energy-dependent contraction (Na+>Li+>K+>choline+) is identical to that of passive swelling in acetate salts, a reaction which is presumed to be dependent on an endogenous cation/H+ exchanger. These results strongly favor an osmotic mechanism for energy-dependent contraction which depends on electrogenic H+ ejection, H+/cation exchange, and electrophoretic anion efflux.     

Evidence for a ‘silent allele’ GLO 0 at the glyoxalase I locus

Summary In a three-generation family, the segregation of an apparent silent allele at the GLO I locus in association with the rare HLA haplotype AW30-CW4-BW35 was observed in four members. In two cases the assumption of homozygosity at the GLO locus would lead to mother-child exclusions. Phenotypically, the GLO activity in the GLO ⁰ carriers is clearly diminished.With rechnical assistance of Mrs. C. Walter and Mrs. M. MuellerSupported by the Deutsche Forschungsgemeinschaft (Ri 164/12)     

A case of ring Y chromosome

Summary Ring Y chromosome 45,X/46,X,r(Y) was identified by fluorescence in a child with ambiguous external genitalia, urogenital sinus, vagina, uterus, and Fallopian tubes. Testicular tissue was noted on gonadal biopsy.     

The effect of culture conditions on the fluidity of mouse neuroblastoma membranes as estimated by spin label studies

Gas chromatography and spin labeling were used to estimate the composition and fluidity of the lipid acyl chains in intact cell membranes of mouse C1300 neuroblastoma. Neurite formation and an increase in the specific activity of acetylcholinesterase are induced in this cell line by the removal of serum from the culture medium for one day prior to harvesting the cells. The fatty acid composition of induced cells was not significantly different from that of the non-induced controls. Each of the three fatty acid spin labels used in this study indicate that the membranes of induced cells are slightly more fluid than the membranes of control cells. This difference in fluidity appears to be a result of a reduction in the progressive decrease in fluidity occurring during growth in serum. A four-fold reduction in cell viability had no effect on the measured bilayer fluidity. Thus the changes in fluidity appear to be due to the presence or absence of serum rather than to cell type, age, or viability.     

Properties and Functions of a New Nucleolar Protein,Surf-6, in 3T3 Mouse Cells

The localization of the specific protein Surf-6 from nucleoli of eukaryotic cells in mitosis and its sensitivity to the treatment of cells with RNase A and DNase I in situ were studied. It was shown that, in interphase nucleoli of 3T3 mouse cells, Surf-6 is probably associated with RNA and practically is not associated with DNA. In mitosis, Surf-6 appears in forming nucleoli after the known RNA-binding proteins fibrillarin and B23/nucleofozmin, which are involved in the early and late stages of the assembly of ribosomal particles, respectively. These observations and the regularities of migration of early and late proteins of ribosome assembly to nucleoli in the telophase of mitosis led us to the presumption that Surf-6 is involved in the terminal stages of the assembly of ribosomal particles in murine cells. An immunoblot analysis of the Surf-6 content in synchronized 3T3 cells showed for the first time that Surf-6 is present at all stages of the cell cycle but its content markedly decreases when cells enter the G0 period. Conversely, the activation of cells for proliferation is accompanied by an increase in the Surf-6 content. These observations allow one to regard Surf-6 as a marker of the cell proliferative state and suggest its implication in the regulation of the cell cycle.     

The establishment of Neisseria meningitidis serogroup W135 of the clonal complex ET-37/ST-11 as an epidemic clone and the persistence of serogroup A isolates in Burkina Faso

We analyzed 48 invasive isolates of Neisseria meningitidis that were isolated from meningitis cases in Burkina Faso (April 2002 to April 2003). Thirty-nine of these isolates had the phenotype (serogroup:serotype:serosubtype) W135:2a:P1.5,2, eight isolates were A:4:P1.9 and one isolate was nongroupable:nonserotypable:nonserosubtypable. Genotyping of meningococcal isolates showed that W135 isolates belonged to the sequence type (ST)-11. The nongroupable isolate was of genogroup W135 and belonged to ST-192. Isolates of serogroup A belonged to ST-2859 (a member of the subgroup III/ST-5 clonal complex). W135 (ST-11) isolates involved in meningitis outbreaks in Burkina Faso differed from those involved in the Hajj-2000 associated outbreak by their pulsed-field gel electrophoresis profile. These data confirm the changing epidemiology of meningococcal infection in Burkina Faso with the establishment and expansion of serogroup W135 N. meningitidis strains of the ET-37/ST-11 clonal complex, as well as the emergence of a new clone within the subgroup III/ST-5 clonal complex.     

An approach for modelling the mean fine-root biomass of Norway spruce stands

The applicability of a heuristic model for estimating mean fine-root biomass of Norway spruce stands based on the coordinates and the diameters at breast height (diameter at a height of 1.3 m, dbh) of their trees was tested. The model was developed based on the following assumptions which were derived from the literature: (1) the maximum distance the roots of a tree can be found depends on the dimension of the tree and exceeds the edges of the crown; (2) fine-root biomass decreases with increasing distance from the tree trunk; (3) fine-root biomass increases with the dbh; (4) maximum fine-root biomass of a tree is not allocated directly around the trees trunk but at some distance from the stem. On the basis of these assumptions the model calculates a relative fine-root biomass at a given point within a stand. Four different versions of the model were compared, with each version differing with respect to the assumed decrease in fine roots with decreasing dbh and the approaches used to calculate the contribution of a subject tree to the fine-root biomass at a given point within a stand (additive versus consumptive). Using regression analysis we parameterised each model type with the data of 70 soil cores from a 75-year-old Norway spruce stand in southern Germany (Bavaria). The relative fine-root biomass calculated by the four different model types accounted for 62–72% of the variation of the measured fine-root biomass. The parameterised models were used to predict the fine-root biomass of 60 given points of a second Norway spruce stand based on its dbhs and stem coordinates. The comparison of measured and predicted mean fine-root biomasses of the second stand revealed no significant differences between the measured mean and the means estimated by three of the four model types. Whereas with two of the model types we achieved means and medians, respectively, nearly identical to the measured average, none of the model types was able to predict values as high as the measured maximum. Constraints of the models and points that need to be considered regarding the minimum number of soil cores needed for a reliable parameterisation of the model are discussed.     

Native and exotic Amphipoda and other Peracarida in the River Meuse: new assemblages emerge from a fast changing fauna

Samples issued from intensive sampling in the Netherlands (1992–2001) and from extensive sampling carried out in the context of international campaigns (1998, 2000 and 2001) were revisited. Additional samples from artificial substrates (1992–2003) and other techniques (various periods) were analysed. The combined data provide a global and dynamic view on the Peracarida community of the River Meuse, with the focus on the Amphipoda. Among the recent exotic species found, Crangonyx pseudogracilisis regressing, Dikerogammarus haemobaphesis restricted to the Condroz course of the river, Gammarus tigrinusis restricted to the lowlands and seems to regress, Jaera istriis restricted to the ‘tidal’ Meuse, Chelicorophium curvispinumis still migrating upstream into the Lorraine course without any strong impact on the other amphipod species. After a rapid expansion Dikerogammarus villosushas continued its upstream invasion between 1998 and 2002 at a rate of 30–40 km per year, but no further progression was noticed in 2003. Locally and temporarily the native species (Gammarus fossarum and G. pulex) and naturalized species (G. roeseliand Echinogammarus berilloni)mayhave been excluded by the most recent invaders (mainly D. villosus), but none of the native and naturalized species has disappeared completely. Therefore, the number of amphipod species found in the River Meuse has increased. Moreover, the native and naturalized species keep on dominating the tributaries from which the recent invaders seem to be excluded. A changing Peracarida community structure is observed along the course of the River Meuse: four native or naturalized species inhabit the upstream (Lorraine) course, three invasive species dominate in the middle reach (Ardenne-Condroz zone), one exotic species is housed in the Border Meuse and three or four invasive species dominate the assemblages in the lowlands.     

Neuroligins mediate excitatory and inhibitory synapse formation: involvement of PSD-95 and neurexin-1beta in neuroligin-induced synaptic specificity

The balance between excitatory and inhibitory synapses is a tightly regulated process that requires differential recruitment of proteins that dictate the specificity of newly formed contacts. However, factors that control this process remain unidentified. Here we show that members of the neuroligin (NLG) family, including NLG1, NLG2, and NLG3, drive the formation of both excitatory and inhibitory presynaptic contacts. The enrichment of endogenous NLG1 at excitatory contacts and NLG2 at inhibitory synapses supports an important in vivo role for these proteins in the development of both types of contacts. Immunocytochemical and electrophysiological analysis showed that the effects on excitatory and inhibitory synapses can be blocked by treatment with a fusion protein containing the extracellular domain of neurexin-1beta. We also found that overexpression of PSD-95, a postsynaptic binding partner of NLGs, resulted in a shift in the distribution of NLG2 from inhibitory to excitatory synapses. These findings reveal a critical role for NLGs and their synaptic partners in controlling the number of inhibitory and excitatory synapses. Furthermore, relative levels of PSD-95 alter the ratio of excitatory to inhibitory synaptic contacts by sequestering members of the NLG family to excitatory synapses.     

The permeability transition pore as a pathway for the release of mitochondrial DNA

This study shows that under oxidative stress DNA from liver mitochondria (mtDNA) can be released through the non-specific permeability transition pore. Pore opening was induced after the addition of Fe2+ and hydrogen peroxide, in the presence of calcium ions. Under these conditions mitochondria undergo large extent swelling, accompanied by the generation of thiobarbituric acid-reactive substances. It was observed that mtDNA was hydrolyzed after the oxidative stress, and it is proposed that some of the fragments were released from the matrix, in such a way that approximately 12% of the total mtDNA remained in the mitochondria. The remaining genetic material was analyzed, after its extraction in an agarose gel. The fragments released were smaller that 1000 bp, by analysis in a native 8% polyacrilamide gel. The presence of cyclosporin A, that inhibited permeability transition, also inhibited mtDNA release by roughly 52%.