Matrilins mediate weak cell attachment without promoting focal adhesion formation.

The matrilins form a family of non-collagenous adaptor proteins in the extracellular matrix. The extracellular ligand interactions of matrilins have been studied in some detail, while the potential interplay between matrilins and cells has been largely neglected. Except for matrilin-4, all matrilins mediate cell attachment, but only for matrilin-1 and -3 the binding is clearly dose dependent and seen already at moderate coating concentrations. Even so, much higher concentrations of matrilin-1 or -3 than of fibronectin are required for cell attachment to reach plateau values. Integrins contribute to the matrilin-mediated cell attachment, but the binding does not lead to formation of focal contacts and reorganisation of the actin cytoskeleton. Cells deficient in beta1 integrins are able to adhere, although weaker, and matrilins do not bind the soluble integrin alpha1beta1 and alpha2beta1 ectodomains. Cell surface proteoglycans may promote the attachment, as cells deficient in glycosaminoglycan biosynthesis adhere less well to matrilin-3. Even so, exogenous glycosaminoglycans are not able to compete for the attachment of HaCaT cells to matrilins.     

Protective Role of the Virus-Specific Immune Response for Development of Severe Neurologic Signs in Simian Immunodeficiency Virus-Infected Macaques

The pathogenesis of human immunodeficiency virus-associated motor and cognitive disorders is poorly understood. In this context both a protective and a harmful role of the immune system has been discussed. This question was addressed in the present study by correlating the occurrence of neurologic disease in simian immunodeficiency virus (SIV)-infected macaques with disease progression and the humoral and cellular intrathecal antiviral immune response. Overt neurologic signs consisting of ataxia and apathy were observed at a much higher frequency in rapid progressor animals (6 of 12) than in slow progressors (1 of 7). Whereas slow progressors mounted a strong antiviral antibody (Ab) response as evidenced by enzyme-linked immunosorbent and immunospot assays, neither virus-specific Ab titers nor Ab-secreting cells could be found in the cerebrospinal fluid (CSF) or brain parenchyma of rapid progressors. Similarly, increased infiltration of CD8⁺ T cells and cytotoxic T lymphocytes specific for viral antigens were detected only in the CSF of slow progressors. The finding that neurologic signs develop frequently in SIV-infected macaques in the absence of an antiviral immune response demonstrates that the immune system does not contribute to the development of motor disorders in these animals. Moreover, the lower incidence of neurologic symptoms in slow progressors with a strong intrathecal immune response suggests a protective role of the virus-specific immunity in immunodeficiency virus-induced central nervous system disease.     

The impact of vertebrate and invertebrate predators on a stream benthic community

I assessed the impact of both vertebrate and invertebrate predators on a lotic benthic community in a 1-month-long experiment, using enclosures containing cobble/gravel bottoms, with large-mesh netting that allowed invertebrates to drift freely. Brown trout (Salmo trutta) and leeches (Erpobdella octoculata) were used as predators and four treatments were tested: a predator-free control, leeches only, trout only, and leeches and trout together. A density of 26.7 leeches/m² (20 leeches/enclosure) and 1.3 trout/m² (one trout per enclosure) was stocked into the enclosures. The total biomass of invertebrate prey was significantly lower in the trout and trout plus leech treatments than in the leech and control treatments, which were due to strong negative effects of trout on Gammarus. On the individual prey taxon level, both trout and leeches affected the abundance of Asellus , Baetis and Ephemerella, whereas the abundance of Gammarus was only affected by trout, and the abundance of Orthocladiinae and Limnephilidae was only affected by leeches. In the treatment with trout and leeches together, the abundance of Ephemerella and Baetis was higher than when trout or leeches were alone, which was probably due to predator interactions. Leeches and trout had no effects on prey immigration but did affect per capita emigration rates. Both trout and leeches indirectly increased periphyton biomass in enclosures, probably due to their strong effects on grazers. Both trout and leeches were size-selective predators, with trout selecting large prey, and leeches selecting small prey. Size-selective predation by trout and leeches affected the size structure of five commonly consumed prey taxa. Trout produced prey populations of small sizes owing to consumption of large prey as well as increased emigration out of enclosures by these large prey. Leech predation produced prey assemblages of larger size owing to consumption and increased emigration of small prey. These results suggest that in lotic habits, predatory invertebrates can be as strong interactors as vertebrate predators. Received: 23 June 1997 / Accepted: 4 May 1998     

Molecular genetic evidence for extracytoplasmic localization of sulfur globules in Chromatium vinosum

Purple sulfur bacteria store sulfur as intracellular globules enclosed by a protein envelope. We cloned the genes sgpA, sgpB, and sgpC, which encode the three different proteins that constitute the sulfur globule envelope of Chromatium vinosum D (DSMZ 180^T). Southern hybridization analyses and nucleotide sequencing showed that these three genes are not clustered in the same operon. All three genes are preceded by sequences resembling σ⁷⁰-dependent promoters, and hairpin structures typical for rho-independent terminators are found immediately downstream of the translational stop codons of sgpA, sgpB, and sgpC. Insertional inactivation of sgpA in Chr. vinosum showed that the presence of only one of the homologous proteins SgpA and SgpB suffices for formation of intact sulfur globules. All three sgp genes encode translation products which – when compared to the isolated proteins – carry amino-terminal extensions. These extensions meet all requirements for typical signal peptides indicating an extracytoplasmic localization of the sulfur globule proteins. A fusion of the phoA gene to the sequence encoding the proposed signal peptide of sgpA led to high specific alkaline phosphatase activities in Escherichia coli, further supporting the envisaged targeting process. Together with electron microscopic evidence these results provide strong indication for an extracytoplasmic localization of the sulfur globules in Chr. vinosum and probably in other Chromatiaceae. Extracytoplasmic formation of stored sulfur could contribute to the transmembranous Δp that drives ATP synthesis and reverse electron flow in Chr. vinosum. Received: 1 October 1997 / Accepted: 17 December 1997     

Sulfide oxidation in the phototrophic sulfur bacterium Chromatium vinosum

Sulfide oxidation in the phototrophic purple sulfur bacterium Chromatium vinosum D (DSMZ 180^T) was studied by insertional inactivation of the fccAB genes, which encode flavocytochrome c, a protein that exhibits sulfide dehydrogenase activity in vitro. Flavocytochrome c is located in the periplasmic space as shown by a PhoA fusion to the signal peptide of the hemoprotein subunit. The genotype of the flavocytochrome-c-deficient Chr. vinosum strain FD1 was verified by Southern hybridization and PCR, and the absence of flavocytochrome c in the mutant was proven at the protein level. The oxidation of thiosulfate and intracellular sulfur by the flavocytochrome-c-deficient mutant was comparable to that of the wild-type. Disruption of the fccAB genes did not have any significant effect on the sulfide-oxidizing ability of the cells, showing that flavocytochrome c is not essential for oxidation of sulfide to intracellular sulfur and indicating the presence of a distinct sulfide-oxidizing system. In accordance with these results, Chr. vinosum extracts catalyzed electron transfer from sulfide to externally added duroquinone, indicating the presence of the enzyme sulfide:quinone oxidoreductase (EC 1.8.5.-). Further investigations showed that the sulfide:quinone oxidoreductase activity was sensitive to heat and to quinone analogue inhibitors. The enzyme is strictly membrane-bound and is constitutively expressed. The presence of sulfide:quinone oxidoreductase points to a connection of sulfide oxidation to the membrane electron transport system at the level of the quinone pool in Chr. vinosum. Received: 5 November 1997 / Accepted: 30 March 1998     

Osmotically reactive plasma membrane vesicles prepared from rabbit kidney tubules by mild hypotonic lysis

Plasma membrane vesicles were obtained by hypotonic lysis in an ice-cold medium containing EDTA and MgCl₂. The vesicles were isolated by differential centrifugation. Compared to a total kidney homogenate, a 10–12-fold enrichment of trehalase and alkaline phosphatase (marker enzymes for renal brush border), and a 6-fold enrichment of (Na⁺---:K⁺)-stimulated ATPase, (a marker enzyme for the basal and lateral plasma membrane of the tubule cell), was achieved. Contamination by other cell organelles was very low. The plasma membrane vesicles enclosed small amounts of the cytoplasmic enzymes lactate dehydrogenase and malate dehydrogenase, which exhibited full activity only after their release into the medium by sonication.Electron micrographs of this preparation showed microvilli with drumstick-like expansions, but also spherical vesicles. By measuring the distribution of radio-actively labelled compounds of different molecular weight in a packed sediment of the plasma membranes under isotonic conditions, an intravesicular volume of 82% or 9 μl/mg of membrane protein was estimated. The intravesicular volume decreased when the osmolality of the medium was augmented by raffinose. The scattering of light by the vesicular suspension could be used to monitor rapid volume changes. By this method, the following sequence of flux rates was established: glycerol>erythritol> adonitol>mannitol. The fluxes of LiCl, NaCl, and KCl were almost identical, but faster than those of adonitol and mannitol. The data indicate, that a large fraction of the plasma membrane isolated in this preparation have formed vesicles, and also that they have retained, as far as investigated, the permeability characteristics of the plasma membrane.     

Beziehungen zwischen Struktur und chemischer Zusammensetzung der Spermien vom Bergmolch,Triturus alpestris Laur.

Zusammenfassung Aus isolierten Achsenfäden der Spermien von Triturus alpestris Laur. wurden drei Proteinfraktionen extrahiert und nach ihrer Zusammensetzung analysiert. In der leichtlöslichen Fraktion f3 überwog Arginin, daneben fand sich u.a. Cystin. f1+f2b enthielt weniger Arginin, dafür aber mehr Lysin. Den größten Anteil hatte hier Alanin. In jeder der beiden Fraktionen waren nur neun Aminosäuren vorhanden. Die schwerlösliche Fraktion c3 enthielt außer Cystin, Methionin und Tyrosin alle nachweisbaren Aminosäuren. Außerdem wies die Fraktion f1+f2b nicht weniger als fünf unbekannte Komponenten auf, von denen eine ein hellgrüner Farbstoff war. In geringeren Mengen kamen drei dieser Substanzen in f3 und noch eine in c3 vor. Nach den Ergebnissen des enzymatischen Abbaus an Ultradünnschnitten von glutaraldehydfixiertem Material dürfte die argininreiche Fraktion im Inneren des Achsenfadens, und zwar in seinem distalen Anteil zu lokalisieren sein. Die lysinreiche Fraktion wäre demnach im Inneren des proximalen Anteils zu finden, während die schwerlösliche Komponente c3 mit der außerordentlich widerstandsfähigen Rinde des Achsenfadens identisch wäre. Im Halsstück, das aus einem kristallinen Mantel und einem homogenen elektronendichten zentralen Teil besteht, fanden sich mindestens drei Komponenten. Der Mantel enthielt ein leicht extrahierbares Protein und ein stabiles Gerüst, in dem aromatische Aminosäuren vermehrt vorzukommen scheinen. Der zentrale Teil bestand aus argininreichen Verbindungen. Die Befunde werden im Zusammenhang mit der Bildung von Achsenfaden und Halsstück während der Spermiogenese diskutiert.

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Relationships between structure and chemical composition of spermatozoa of the newt, Triturus alpestris Laur.

Summary Axial rods from spermatozoa of Triturus alpestris Laur. have been isolated. Three protein fractions therefrom could be extracted and analysed for their composition. Arginine prevailed in the soluble fraction f3, among others also cystine was found. f1+f2b contained less arginine, but more lysine. The highest percentage was found here for alinine. In each of the two fractions only nine amino acids were present. The sparely soluble fraction c3 contained all identifiable amino acids besides cystine, methionine and tyrosine. Moreover, the fraction f1+f2b showed as many as five unknown components, from which one was a light-green colour. To a lesser degree three of these compounds were also found in fraction f3 and still one in fraction c3. According to the results of the enzymatic digestion carried out on ultrathin section of material fixed with glutaraldehyde, the arginine-rich fraction should be localized in the center of the axial rod in its distal part. The lysine-rich fraction would then be found in the center of the proximal part, while the sparely soluble fraction c3 would be identical with the extremely resistant cortex of the axial rod. Within the neck-piece, which consists of a crystalline mantle and a homogenously dark central part, at least three components were present. The mantle contained an easily extractable protein and a stable frame, in which aromatic amino acids seemed to be increased. In the central part arginine prevailed. The results are discussed with regard to the formation of the axial rod and the neck-piece during spermiogenesis.

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Mit dankenswerter Unterstützung durch die Deutsche Forschungsgemeinschaft.