Immunocytochemical Distribution of 5-HT (Serotonin) in the Nervous System of the Gastrotrich Turbanella cornuta

The 5-HT (serotonin) distribution in the nervous system of the macrodasyoid gastrotrich Turbanella cornuta was studied using immunocytochemical methods. Positive immunoreaction was found in two pairs of neurons. The neurons of one pair had processes which extended peripherally to the surface of the body. Central processes of both pairs entered the brain commissure and proceeded into the longitudinal cords. Unlike other acoelomate worms studied so far, the Platyhelminthes and the Nematoda, in this gastrotrich no 5-HT positive perikarya or processes were present in the pharynx innervation, and no positive neurons sent processes directly to the nerve cords     

Clinical and Molecular Characterization of Patients with Distal 11q Deletions

Jacobsen syndrome is caused by segmental aneusomy for the distal end of the long arm of chromosome 11. Typical features include mild to moderate psychomotor retardation, trigonocephaly, facial dysmorphism, cardiac defects, and thrombocytopenia, though none of these features are invariably present. To define the critical regions responsible for these abnormalities, we studied 17 individuals with de novo terminal deletions of 11q. The patients were characterized in a loss-of-heterozygosity analysis using polymorphic dinucleotide repeats. The breakpoints in the complete two-generation families were localized with an average resolution of 3.9 cM. Eight patients with the largest deletions extending from 11q23.3 to 11qter have breakpoints, between D11S924 and D11S1341. This cytogenetic region accounts for the majority of 11q⁻ patients and may be related to the FRA11B fragile site in 11q23.3. One patient with a small terminal deletion distal to D11S1351 had facial dysmorphism, cardiac defects, and thrombocytopenia, suggesting that the genes responsible for these features may lie distal to D11S1351. Twelve of 15 patients with deletion breakpoints as far distal as D11S1345 had trigonocephaly, while patients with deletions distal to D11S912 did not, suggesting that, if hemizygosity for a single gene is responsible for this dysmorphic feature, the gene may lie distal to D11S1345 and proximal to D11S912.     

Isolation and characterization of mosquito ferritin and cloning of a cDNA that encodes one subunit

Ferritin, an iron storage protein, was isolated from larvae and pupae of Aedes aegypti grown in an iron-rich medium. Mosquito ferritin is a high molecular weight protein composed of several different, relatively small, subunits. Subunits of molecular mass 24, 26, and 28 kDa are equally abundant, while that of 30 kDa is present only in small amounts. The N-terminal sequence of the 24 and 26 kDa subunits are identical for the first 30 amino acids, while that of the 28 kDa subunit differs. Studies using antiserum raised against a subunit mixture showed that the ferritin subunits were present in larvae, pupae, and adult females, and were increased in animals exposed to excess iron. The antiserum also was used to screen a cDNA library from unfed adult female mosquitoes. Nine clones were obtained that differed only in a 27 bp insertion in the 3′ end. Rapid amplification of cDNA ends (RACE) was used to obtain the complete protein coding sequence. A putative iron-responsive element (IRE) is present in the 5′-untranslated region. The deduced amino acid sequence shows a typical leader sequence, consistent with the fact that most insect ferritins are secreted, rather than cytoplasmic proteins. The sequence encodes a mature polypeptide of 20,566 molecular weight, smaller than the estimated size of any of the subunits. However, the sequence exactly matches the N-terminal sequences of the 24 and 26 kDa subunits as determined by Edman degradation. Of the known ferritin sequences, that of the mosquito is most similar to that of somatic cells of a snail. © 1995 Wiley-Liss, Inc.     

Serological detection of H-2K- and H-2D-gene products

Using the fluorescence-activated cell sorter (FACS II), we have analyzed the expression of H-2K- and H-2D-gene products on the membrane of various cellular components of the murine immune system. Using this serological technique we show a basic difference between T and B lymphocytes. Whereas all cellular components analyzed — hydrocortisone-resistant thymocytes, splenic T and B lymphocytes, macrophages and bone-marrow cells — expressed H-2K-subregion-encoded alloantigens at a high density, it seems that the high density expression of H-2D-encoded alloantigens is restricted mainly to B cells and to macrophages. Hydrocortisone-resistant thymocytes, splenic T lymphocytes and bone-marrow cells, on the other hand, showed significant expression of the H-2D alloantigens only at low membrane density. These results, then, provide evidence for the existence of an imbalance in serologically detectable expression of H-2K- and H-2D-region-gene products on the cell membrane of various cells comprising the murine immune system.Abbreviations usedin this paper DTH delayed type hypersensitivity - FCS fetal calf serum - FITC fluorescein isothiocyanate - HrT hydrocortisone-resistant thymocytes - Ig immunoglobulins P. De Baetselier is an EMBO and Euratom postdoctoral fellow     

Action of surfactants on egg lecithin liposomes

The lytic action of several homologous series of surfactants including N-acyl derivatives of the Na-salt of amino acids on the egg lecithin multilamellar liposomes was examined. The affinity for the lipid membrane and the solubilising capacity of the agents were estimated. The contribution of a CH₂ group and that of the polar head group of surfactants to the free energy of the agent's binding to the membrane were evaluated. The results obtained indicate that the contribution of a CH₂ group to the free binding energy depends on the nature of the surfactants' head group. This dependence is attributed to either various localisation of the agent's molecules in the lipid bilayer or to different properties of the agent's hydrocarbon tails. The contributions of the head groups of the surfactants are assumed to reflect the affinity of these head groups for the lecithin polar head group at the membrane interface. The results obtained indicate some degree of specificity involved in the interactions of the head groups.     

Direct current electric field in some teleost species: Effect of medium salinity

Summary A direct current electric field up to 3 mV/ cm was recorded in 33 sea water around the fishMyoxocephalus brandti, Hexogrammos octogrammos, Enophrys diceraus, Pleuronectes stellatus, Bathimaste r derjugini, Sebastes scorpaeniformis. The body surface potentials were positive in relation to the external and internal media; they attained 10 mV and slowly varied near the mean value at every point. The potentials at the surface points of individual skin sections adjoining the oral and branchial cavities, the anal orifice and peripheral fin sections were normally characterized by polarities opposite to those of body surface potentials (in sea water they were negative in relation to the external medium).When placed in sea water during their fresh water cycle, the salmonOncorhynchus keta and the fresh water fishSalvelinus alpinus andMisgurnus fossilis had no d.c. field.In fresh water containing less than 0.03 salt, a d.c. field up to 25 mV/cm was recorded around all the above mentioned species. The potentials had an opposite polarity to that recorded in sea water.The distribution of potentials over the fish surface depends on the species. The potentials at some points of the body surfaces were found to vary when other fish or metal objects were placed in the aquarium.The parameters of the direct current electric field generated by a whole fish and by isolated skin pieces were identical and varied by the same law with changed medium salinity. Thus it may be assumed that the d.c. electric field around the fish is produced by active electrogenic ion transport mechanisms localized in the skin.     

Comparative primary productivity of algal epiphytes on three species of macrophyte in the littoral zone of Lake Ohrid, Yugoslavia

Primary productivity of algal epiphytes on the surfaces of Phragmites, Potamogeton , and Nuphar was measured seasonally from June 1978, through June 1979, in the littoral zone of Lake Ohrid, using ¹⁴C methodology. Surface areas of individual macrophytes were determined throughout the study period through the use of a non-miscible surfactant and a calibration curve of surfactant weight versus known, calculated surface areas.
Mean total surface area available for epiphytic colonization during the study period was 1.032 m² macrophyte surface per m² of littoral zone for Phragmites , 0.810 m² for Potamogeton , and 0.167 m² for Nuphar . Seasonal rates of mean primary productivity of algal epiphytes on Phragmites from the surface to the light-compensation depth ranged from 84–1406 mg C m⁻² littoral zone d⁻¹; ranges for epiphytes on Potamogeton and Nuphar were 77–586 and 69–268 mg C m⁻² littoral zone d⁻¹, respectively. Maximum rates were observed typically during June; minimum rates were observed typically during August to December. Mean daily productivity rates over the 12 month period were for epiphytes on Potamogeton 167.0, on Nuphar 100.4 and on Phragmites 671.2 mg C m⁻² littoral zone d⁻¹. Calculated annual production for epiphytes on Nuphar was 36.65, on Potamogeton 60.95 and on Phragmites 245.0 g C m⁻² littoral zone yr⁻¹. Epiphytic production data were typically considerably higher than production data obtained for littoral and pelagial planktonic algae and compare favorably with published data for epiphytic and periphytic production in Lawrence Lake, Marion Lake, and Borax Lake.     

Co-purification of soluble human galactosyltransferase and immunoglobulins

Preparations of human malignant effusion galactosyltransferase activity purified according to previously published techniques using enzyme-specific affinity chromatography consistently produced antibodies directed toward immunoglobulins with no detectable antigalactosyltransferase. Double immunodiffusion analysis of the antigen showed the presence of both IgG and IgA. Affinity chromatography with anti-human IgG-Sepharose and anti-human serum-Sepharose resulted in a 48,000-fold purification of galactosyltransferase activity with no detectable IgG by radioimmunoassay. Immunization of rabbits with this preparation produced antibodies directed against galactosyltransferase activity and minimal anti-Ig. The persistence of immunoglobulins during the purification of soluble galactosyltransferase activity through two enzyme-specific affinity chromatographic steps suggests an association of immunoglobulins with galactosyltransferase activity.     

Block-synthesis of higher oligosaccharides: Synthesis of hexa- and nona-saccharide fragments of the o-antigenic polysaccharide of Salmonella newington

Successive condensation of derivatives of the trisaccharide, biological repeating-unit of the O-antigenic polysaccharide of Salmonella newington, followed by removal of protecting groups, has given the hexa- and nona-saccharides. The structures of these oligosaccharides were confirmed chemically and by ¹³C-n.m.r. spectroscopy.     

Molecular genetic analysis of the Escherichia coli phoP locus.

We have cloned the Escherichia coli phoP gene, a member of the family of environmentally responsive two-component systems, and found its deduced amino acid sequence to be 93% identical to that of the Salmonella typhimurium homolog, which encodes a major virulence regulator necessary for intramacrophage survival and resistance to cationic peptides of phagocytic cells. The phoP gene was mapped to kilobase 1202 on the Kohara map (25-min region) of the E. coli genome (Y. Kohara, K. Akiyama, and K. Isono, Cell 50:495-508, 1987) and found to be transcribed in a counterclockwise direction. Both E. coli and S. typhimurium phoP mutants were more sensitive than their isogenic wild-type strains to the frog-derived antibacterial peptide magainin 2, suggesting a role for PhoP in the response to various stresses in both enteric species.