Characterization of Lymphocyte Fibronectin

In vitrocultured “activated” peripheral blood lymphocytes and T-cell lines synthesized a high-molecular-weight gelatin binding molecule (MW 500 kDa), whereas resting lymphocytes showed poor or negligible synthesis of the same component. Concanavalin A-mediated anchorage of the lymphocytes to a substratum potentiated synthesis of the high-molecular-weight molecule. Western blotting of the gelatin-binding lymphocyte molecule demonstrated reactivity with antibodies specific for human fibronectin. Furthermore, immunocytochemistry showed reactivity of anti-fibronectin antibodies with T-lymphocytes at the single-cell level. The lymphocyte-derived fibronectin was preferentially cell associated and relatively small amounts were present in the culture medium. RT-PCR of total RNA from CD4⁺T-cells and the lymphoid T-cell line MOLT-4 showed that the most abundant species of fibronectin mRNA lacked the entire III CS exon encoding the α₄β₁binding region LDV. Amplification of the III CS region from other T-cell lines revealed that these cells expressed several fibronectin mRNA isoforms most of which were lacking the LDV coding sequence. In conclusion, synthesis of fibronectin is demonstrated to occur in T-lymphocytes and to be regulated by signals which activate the cells.     

Lack of correlation between the rate of cholesterol biosynthesis and the activity of 3-hydroxy-3-methylgutaryl coenzyme A reductase in rats and in fibroblasts treated with ML-236B

The phospholipase-2 inhibitor, p-bromophenacyl bromide, has been shown to inhibit strongly the elongation of endogenous fatty acids in preparations of brain mitochondria and microsomes. On the other hand, it does not inhibit the elongation of added palmitic or linoleic acids. The implication is that the normal first step in alteration of membrane lipid fatty acids is their release to other membrane-bound enzyme systems by a membrane-bound phospholipase A.     

Factors controlling the in vitro growth pattern of human microvascular endothelial cells

Monolayer cultures of endothelial cells of human dermal microvascular origin were exposed to a variety of culture conditions and in vitro differentiation of the cells assessed by light and electron microscopic examination. Restoration of a cytologic and fine structural appearance which resembled most closely that present in vivo was possible by raising the intracellular cAMP level. These cells formed junctional complexes seen in uncontracted microvessels and specialized attachment sites at their basal cell membrane, contained a complex network of bundled micro- and intermediate filaments and numerous Weibel-Palade bodies and accumulated electron-opaque deposits between the cells and the culture dish surface.     

Immunoperoxidase staining of glial fibrillary acidic (GFA) protein polymerized in vitro: An ultramicroscopic study

The unlabeled antibody peroxidase-antiperoxidase (PAP) method of Sternberger et al. has been employed at the ultramicroscopic level to stain filaments polymerized in vitro from aqueous extracts of multiple sclerosis (MS) plaques. The filaments were heavily decorated with antiserum to the glial fibrillary acidic (GFA) protein but not stained with serum absorbed with GFA protein, preimmunization serum, or anti-rat brain tubulin antiserum. Reassembled rat brain tubulin was heavily stained with antiserum to tubulin but was not stained with antiserum to the GFA protein. The present study provides direct morphological evidence that filaments polymerized in vitro from extracts of MS plaques contain the GFA protein.     

Ground beetle responses to patch retention harvesting in high elevation forests of British Columbia

The effect of a forest harvesting system whereby small (typically 0.1–2.0 ha) patches of standing timber are retained inside of harvests, was compared to conventional clearcutting for its effect on ground beetle assemblages. Two seasons of pitfall trapping entailed 46 451 trap days, and yielded 15 799 individuals of 28 species; abundance was dominated by four species comprising 92.4% of the catch. Most species were known to have wide geographic distributions in Canada and Alaska but many species seemed to respond to disturbance on a site-specific basis. Contrary to findings of similar studies, no species could be characterized as "mature-forest specialists", or "forest generalists". Forest patches and edge habitats immediately inside the forest canopy contained assemblages more closely related to mature forest than to cleared areas. Harvested areas with patches yielded catches distinct from typical clearcuts, based primarily on changes in abundance of one common species. Climatic regimes and landscape disturbance levels were the two important factors distinguishing our study from others, and we have suggested that these may influence the degree to which patches are an effective conservation tool.     

Varying immunological effects in mice of intranasal infection with different strains of influenza virus

Intranasal infection of CBA/Ca mice with a sublethal dose of A/2 Japan influenza virus 305/57 decreased the blastogenic response to concanavalin A and phytohemagglutinin, and less to lipopolysaccharide andEscherichia coli bacteria. This depression of the blastogenic responses could be transferred from infected donor mice by intravenous injection of 4×10⁷ spleen cells to otherwise untreated syngenic recipient mice. Similar infections with A/Victoria 3/75 and A/Texas 1/77 influenza virus strains caused less depressing effects. Less consistent results were seen with NMRI mice. No impairment of the antibody responses to unrelated protein antigen could be noted after such intranasal influenza infection. In contrast, the IgE antibody response was particularly increased after infection with Texas virus. Some deleterious effects of Victoria and Texas virus infections on the delayed hypersensitivity response to picryl chloride were seen in CBA mice but not in NMRI mice. This immune suppression by virus infection was not reflected by the defense against intraperitoneal infection withListeria monocytogenes andE. coli. In contrast, a small increase in resistance toListeria infection was recorded. The results of this study lend little support to the hypothesis that influenza infection impairs the immunological defense against a following bacterial infection, but may result in allergy.     

ATP level of a starving surface-bound and free-living marine Vibrio sp.

Abstract ATP levels of three marine isolates (a Vibrio sp., Serratia marcescens , and an unidentified rodshaped organism) were measured during nutrient-limiting conditions for free-living bacteria or cells adhered to a glass/liquid interface. In all strains there was a higher content of ATP per biovolume (numbers × cell volume) for cells starved at the glass/liquid interface compared with those in the bulk phase. Leakage from viable cells and the formation of a conditioning film are suggested only partly to explain the elevated levels of ATP per biovolume at the surface.