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Imbalance in the network of soluble mediators may play a pivotal role in the pathogenesis of Kaposi's sarcoma (KS). In this study, we demonstrated that KS cells grown in vitro produced and in part released platelet activating factor (PAF), a powerful lipid mediator of inflammation and cell-to-cell communication. IL-1, TNF, and thrombin enhanced the synthesis of PAF. PAF receptor mRNA and specific, high affinity binding site for PAF were present in KS cells. Nanomolar concentration of PAF stimulated the chemotaxis and chemokinesis of KS cells, endothelial cells, and vascular smooth muscle cells. The migration response to PAF was inhibited by WEB 2170, a hetrazepinoic PAF receptor antagonist. Because neoangiogenesis is essential for the growth and progression of KS and since PAF can activate vascular endothelial cells, we examined the potential role of PAF as an instrumental mediator of angiogenesis associated with KS. Conditioned medium (CM) from KS cells (KS-CM) or KS cells themselves induced angiogenesis and macrophage recruitment in a murine model in which Matrigel was injected subcutaneously. These effects were inhibited by treating mice with WEB 2170. Synthetic PAF or natural PAF extracted from plasma of patients with classical KS also induced angiogenesis, which in turn was inhibited by WEB 2170. The action of PAF was amplified by expression of other angiogenic factors and chemokines: these included basic and acidic fibroblast growth factor, placental growth factor, vascular endothelial growth factor and its specific receptor flk-1, hepatocyte growth factor, KC, and macrophage inflammatory protein-2. Treatment with WEB 2170 abolished the expression of the transcripts of these molecules within Matrigel containing KS-CM. These results indicate that PAF may cooperate with other angiogenic molecules and chemokines in inducing vascular development in KS.

Juvenile Atlantic salmon (Salmo salar) meristic and morphometric characteristics were examined from 47 European and North American river populations. The relative importance of continental origin, stream gradient, overall temperature regime, and seasonal temperatures in explaining the phenotypic variation of these populations was evaluated using multi-way ANOVA. Ecological factors explained a greater percentage of the variance than continental origin for both meristic and morphometric characters. Stream gradient was the most important factor explaining morphometric variation and April-May mean temperature was the most important factor explaining meristic variation.

Since the mid-19th century, numerous attempts have been made to restore or enhance populations of the Atlantic salmon, Salmo salar, within the endemic range, and to establish the species in other parts of the world. Despite all efforts, salmon have become naturalized locally only in eastern North America, Argentina, the Faeroe Islands, and New Zealand. Principal factors affecting the disappearance, restoration, or naturalization of populations are water temperature and availability of suitable spawning and nursery sites. Commercial exploitation of the species in coastal and offshore waters is viewed internationally as a factor of increased importance in the numerical regulation of river spawning runs. A further expansion of the world distribution of Atlantic salmon by naturalization seems unlikely except in areas where preliminary plantings have been made or brood stocks are presently held. Atlantic salmon produced by commercial sea farming operations in Norway, Scotland, Spain, and France are considered to be of comparable quality to fish harvested from the wild. Also, there is presently interest in the potential of sea ranching of Atlantic salmon. Key words: zoogeography, endemic range, naturalized range, artificial propagation, environmental impact, exploitation, aquaculture

Effects of various loadings of a test gravel incubation substrate (32- to >4-mm pebble) with a single sediment mix (−1). Mean survival (75%) from ova burial to juvenile emergence was not influenced significantly by different sediment loadings. However, time to first and median emergence, duration of emergence, stage of development at emergence, and within-substrate behaviour were each correlated positively with mean particle size (r ≥ 0.72) and negatively with sediment loading rates (r ≥ −0.68).

Lake trout, Salvelinus namaycush, released into Tadenac Lake as juveniles, show a pronounced acceleration in growth rate, following a change in diet from benthic invertebrates to rainbow smelt, Osmerus mordax, beginning at age 6 (> 30 cm). An abrupt increase in the rate of mercury accumulation in white muscle of these fish occurs at the same time. Mercury levels in lake trout ([Formula: see text] = 0.24–3.44 μg/g) and coresident smelt ([Formula: see text] = 0.06–0.48 μg/g) from Tadenac and eight neighboring lakes reveal maximum levels reaching 10.0 and 0.84 μg/g, respectively. Mercury levels in lake trout from Tadenac Lake, an undisturbed PreCambrian Shield ecosystem without detected indigenous sources, exceed the "safe" level (0.5 μg/g) at sexual maturity and at a size less than generally acceptable for human utilization. Mercury accumulation by the trout is correlated with length (r = 0.92) in each lake population examined, but substantial among-lake differences occur in fish of comparable ages. As the growth rates are similar in various waters, differences in extent of mercury accumulation is attributed to differences in mercury availability among lakes. In view of a strong correlation (r = 0.96) between mercury levels in smelt and trout calculated at standardized length, it is proposed that the smelt is an appropriate indicator species for the ranking of cold-water lakes relative to the availability of mercury for uptake by lake trout and other living aquatic organisms.Key words: mercury uptake, lake trout, rainbow smelt, growth rate, diet

Random samples of rainbow smelt, Osmerus mordax, from commercial summer trawl harvests in the Central and Eastern basins of Lake Erie are examined. Analysis of the meristic, morphometric, and electrophoretic data indicates no statistical evidence of genetic differences between basin populations. However, significant differences in size and growth data between basin populations occur and are attributed to differences in limnological conditions between basins which affect the time of spawning, length of growing season, and growth rate. Thus, these differences indicate an ecophenotypic distinction between the Central and Eastern Basin populations because of between-basin limnological dissimilarities.

This note supplements the original paper by MacCrimmon and Marshall (J. Fish. Res. Bd. Canada 25: 2527–2548, 1968) in presenting modified and more complete information on the native range, attempted introductions, and present world distribution of the brown trout.

This note supplements the original paper by MacCrimmon and Campbell (J. Fish. Res. Bd. Canada 26: 1699–1725, 1969) by presenting additional information on the native range, attempted introductions, and present world distribution of the brook trout.

Human immunodeficiency virus-1 (HIV-1)-Tat, the transactivating gene product of HIV-1, has been shown to interact with different cell types, inducing gene expression, altering their growth and migratory behavior. In this study we examined whether Tat might affect functions of acquired immunodeficiency syndrome (AIDS)-related non-Hodgkin’s lymphoma (NHL), relevant to the in vivo dissemination. Our results show that Tat significantly augmented the motility of the two AIDS-related Burkitt’s lymphoma cell lines (AS283 and PA682PB) and AIDS-primary effusion lymphoma cell line (HBL-6-AIDS-PEL). Mutations in RGD or basic domain of Tat (KGE-MBP and LxI-MBP, respectively) sharply reduced migration compared with wild type, suggesting that both domains are required for migration. In contrast, a Tat protein mutation outside the active domains (NH2-TAT-GST) did not reduce lymphoma cell migration. The treatment of lymphoma cells with Tat did not influence their adhesion to matrix proteins or to human vascular endothelial cells, but endothelial cells treated with Tat became more adhesive to lymphoma cells. Flow cytometric analysis showed that treatment of endothelial cells with Tat induced the cell surface expression of the adhesion molecules vascular cell adhesion molecule-1 (VCAM-1) and E-selectin and increased the expression of intercellular adhesion molecule-1 (ICAM-1). Only antibodies against VCAM-1 on endothelial cells or against the VLA-4 integrin expressed on AS283 cells inhibited the increment of adhesion, indicating the relevance of this pathway in the adhesion of lymphoma cells to vascular endothelium. In our work, we show for the first time that Tat can enhance the migration of lymphoma cells and their adhesion to endothelial cells, two processes that may contribute to the malignant behavior of NHL in patients with AIDS.

Human immunodeficiency virus type 1 (HIV-1) Tat transactivates viral genes and is released by infected cells, acting as a soluble mediator. In endothelial cells (EC), it activates a proangiogenic program by activating vascular endothelial growth factor receptor type 2 (VEGFR-2) and integrins. A structure-activity relationship study was performed by functional analysis of Tat substitution and deletion variants to define the Tat determinants necessary for EC activation. Variants were made (i) in the basic and (ii) in the cysteine-rich domains and (iii) in the C-terminal region containing the RGD sequence required for integrin recognition. Our results led to the following conclusions. (i) Besides a high-affinity binding site corresponding to VEGFR-2, EC express low-affinity binding sites. (ii) The basic and the cysteine-rich variants bind only to the low-affinity binding sites and do not promote tyrosine phosphorylation of VEGFR-2. Furthermore, they have a reduced ability to activate EC in vitro, and they lack angiogenic activity. (iii) Mutants with mutations in the C-terminal region are partially defective for in vitro biological activities and in vivo angiogenesis, but they activate VEGFR-2 as Tat wild type. In conclusion, regions encoded by the first exon oftatare necessary and sufficient for activation of VEGFR-2. However, the C-terminal region, most probably through RGD-mediated integrin engagement, is indispensable for full activation of an in vitro and in vivo angiogenic program.