Hemopoietic cell expression of the chemokine decoy receptor D6 is dynamic and regulated by GATA1

D6 scavenges inflammatory chemokines and is essential for the regulation of inflammatory and immune responses. Mechanisms explaining the cellular basis for D6 function have been based on D6 expression by lymphatic endothelial cells. In this study, we demonstrate that functional D6 is also expressed by murine and human hemopoietic cells and that this expression can be regulated by pro- and anti-inflammatory agents. D6 expression was highest in B cells and dendritic cells (DCs). In myeloid cells, LPS down-regulated expression, while TGF-beta up-regulated expression. Activation of T cells with anti-CD3 and soluble CD28 up-regulated mRNA expression 20-fold, while maturation of human macrophage and megakaryocyte precursors also up-regulated D6 expression. Competition assays demonstrated that chemokine uptake was D6 dependent in human leukocytes, whereas mouse D6-null cells failed to uptake and clear inflammatory chemokines. Furthermore, we present evidence indicating that D6 expression is GATA1 dependent, thus explaining D6 expression in myeloid progenitor cells, mast cells, megakaryocytes, and DCs. We propose a model for D6 function in which leukocytes, within inflamed sites, activate D6 expression and thus trigger resolution of inflammatory responses. Our data on D6 expression by circulating DCs and B cells also suggest alternative roles for D6, perhaps in the coordination of innate and adaptive immune responses. These data therefore alter our models of in vivo D6 function and suggest possible discrete, and novel, roles for D6 on lymphatic endothelial cells and leukocytes.     

The Yin and Yang of treating BRCA-deficient tumors

The myriad changes that occur during the malignant progression of cancer cells present challenges to both clinicians and basic scientists. Two new studies in Nature underscore the central role of genome instability in tumor biology (Edwards et al., 2008; Sakai et al., 2008). These reports describe secondary changes in the BRCA2 locus that restore the wild-type reading frame and contribute to the development of resistance to chemotherapeutic agents.     

First detection, isolation and molecular characterization of infectious salmon anaemia virus associated with clinical disease in farmed Atlantic salmon (Salmo salar) in Chile

Background  

Several forms of progressive retinal atrophy (PRA) segregate in more than 100 breeds of dog with each PRA segregating in one or a few breeds. This breed specificity may be accounted for by founder effects and genetic drift, which have reduced the genetic heterogeneity of each breed, thereby facilitating the identification of causal mutations. We report here a new form of PRA segregating in the Border Collie breed. The clinical signs, including the loss of night vision and a progressive loss of day vision, resulting in complete blindness, occur at the age of three to four years and may be detected earlier through systematic ocular fundus examination and electroretinography (ERG).     

Rosiglitazone stimulates nitric oxide synthesis in human aortic endothelial cells via AMP-activated protein kinase

The thiazolidinedione anti-diabetic drugs increase activation of endothelial nitric-oxide (NO) synthase by phosphorylation at Ser-1177 and increase NO bioavailability, yet the molecular mechanisms that underlie this remain poorly characterized. Several protein kinases, including AMP-activated protein kinase, have been demonstrated to phosphorylate endothelial NO synthase at Ser-1177. In the current study we determined the role of AMP-activated protein kinase in rosiglitazone-stimulated NO synthesis. Stimulation of human aortic endothelial cells with rosiglitazone resulted in the time- and dose-dependent stimulation of AMP-activated protein kinase activity and NO production with concomitant phosphorylation of endothelial NO synthase at Ser-1177. Rosiglitazone stimulated an increase in the ADP/ATP ratio in endothelial cells, and LKB1 was essential for rosiglitazone-stimulated AMPK activity in HeLa cells. Infection of endothelial cells with a virus encoding a dominant negative AMP-activated protein kinase mutant abrogated rosiglitazone-stimulated Ser-1177 phosphorylation and NO production. Furthermore, the stimulation of AMP-activated protein kinase and NO synthesis by rosiglitazone was unaffected by the peroxisome proliferator-activated receptor-gamma inhibitor GW9662. These studies demonstrate that rosiglitazone is able to acutely stimulate NO synthesis in cultured endothelial cells by an AMP-activated protein kinase-dependent mechanism, likely to be mediated by LKB1.     

Integrating ecology with biogeography using landscape characteristics: a case study of subtidal habitat across continental Australia

Aim We aimed to redress a current limitation of local ecological studies (i.e. piecemeal information on specific taxa) by integrating existing ecological knowledge with quantifiable patterns in primary habitat (i.e. composition, distribution and cover) from local to continental scales. By achieving this aim, we sought to provide a biogeographical framework for the interpretation of variation in the ecology of, and threats to, subtidal rocky landscapes. Location The subtidal rocky coast of continental Australia, with longitudinal comparisons spanning > 4000 km of southern coast (115°03′ E–153°60′ E) between latitudes of 33°05′ S and 35°36′ S, and latitudinal comparisons across 26°40′ S to 37°08′ S of eastern Australia. Methods The frequency and size of patches of major benthic habitat were quantified to indicate contemporary function (ecology) and to establish patterns that may result from contrasting regional‐scale processes (biogeography). This was achieved by quantifying the composition and patchiness of key subtidal habitats across the continent and relating them to the known ecology of subsets of locations in each region. A nested design of several spatial scales (1000s, 100s, 10–1 km) was adopted to distinguish patterns at local through to biogeographical scales. Results We show biogeography (in terms of longitude and latitude) to have a fundamental influence on the patterns of abundance and composition of subtidal habitats across regional (1000s of kilometres) to local (10s of kilometres to metres) scales. Across the continent, the most fundamental patterns related to (1) the proportion of rock covered by kelp forests, as related to particular functional groups of herbivores, and (2) the small‐scale heterogeneity (metres) that characterizes these forests. Main conclusions We interpret these results within a framework of alternative processes known to maintain habitat heterogeneity across these regions (e.g. productivity versus consumption as shapers of habitat structure). These interpretations illustrate how regional differences in ecological patterns and processes can create contradictory outcomes for the management of natural resources. We suggest that researchers and managers of natural resources alike may benefit from understanding local issues (e.g. the effects of fishing and its synergies with water pollution) in their biogeographical contexts.     

Interactive effects of shade and surface orientation on the recruitment of spirorbid polychaetes

A series of observations and an experiment were carried out to test hypotheses about the effects of shade on the densities of spirorbid polychaetes (Neodexiospira spp.) on intertidal pneumatophores (mangrove roots) of Avicennia marina. Densities of spirorbids were greater on pneumatophores surrounded by seagrass (Zostera mucronata) than patches without seagrass. Within patches of seagrass, the density and survivorship of spirorbids on pneumatophores was greater near the substratum (covered by seagrass) than high above the substratum (not covered by seagrass). The model that these patterns of abundance are explained by greater recruitment of spirorbids to shaded surfaces was assessed. This was done by experimentally testing the hypothesis that recruitment to patches without seagrass would not differ between the upper (unshaded) and lower surfaces (unshaded) of clear plastic sheets, but would be greater on the lower surfaces (shaded) than upper surfaces (unshaded) of black plastic sheets. Recruitment was consistent with these predictions and therefore provided evidence that differences in densities of spirorbids between substrata with and without seagrass may be due largely to differences in shading.     

EPA,not DHA,prevents fibrosis in pressure overload-induced heart failure: potential role of free fatty acid receptor 4

Heart failure with preserved ejection fraction (HFpEF) is half of all HF, but standard HF therapies are ineffective. Diastolic dysfunction, often secondary to interstitial fibrosis, is common in HFpEF. Previously, we found that supra-physiologic levels of ω3-PUFAs produced by 12 weeks of ω3-dietary supplementation prevented fibrosis and contractile dysfunction following pressure overload [transverse aortic constriction (TAC)], a model that resembles aspects of remodeling in HFpEF. This raised several questions regarding ω3-concentration-dependent cardioprotection, the specific role of EPA and DHA, and the relationship between prevention of fibrosis and contractile dysfunction. To achieve more clinically relevant ω3-levels and test individual ω3-PUFAs, we shortened the ω3-diet regimen and used EPA- and DHA-specific diets to examine remodeling following TAC. The shorter diet regimen produced ω3-PUFA levels closer to Western clinics. Further, EPA, but not DHA, prevented fibrosis following TAC. However, neither ω3-PUFA prevented contractile dysfunction, perhaps due to reduced uptake of ω3-PUFA. Interestingly, EPA did not accumulate in cardiac fibroblasts. However, FFA receptor 4, a G protein-coupled receptor for ω3-PUFAs, was sufficient and required to block transforming growth factor β1-fibrotic signaling in cultured cardiac fibroblasts, suggesting a novel mechanism for EPA. In summary, EPA-mediated prevention of fibrosis could represent a novel therapy for HFpEF.