Lipocortin 1 reduces myocardial ischemia-reperfusion injury by affecting local leukocyte recruitment.

We assessed here the effect of the glucocorticoid-regulated protein lipocortin 1 (LC1) in a model of rat myocardial ischemia reperfusion. Treatment of animals with human recombinant LC1 at the end of a 25-min ischemic period significantly reduced the extent of infarct size in the area at risk as measured 2 h later, with approximately 50% inhibition at the highest dose tested of 50 microg per rat (equivalent to 5.4 nmol/kg). The protective effect of LC1 was abolished by protein denaturation and not mimicked by the structurally related protein annexin V. A combination of electron and light microscopy techniques demonstrated the occurrence of the myocardial damage at the end of the reperfusion period, with loss of fiber organization. LC1 provided a partial and visible protection. The dose-dependent protection afforded by LC1 was paralleled by lower values of myeloperoxidase activity, tumor necrosis factor a, and macrophage inflammatory protein-1a. The functional link between migrated leukocytes and the myocardial damage was confirmed by electron and light microscopy, and a significantly lower number of extravasated leukocytes was counted in the group of rats treated with LC1 (50 microg). In conclusion, we demonstrate for the first time that LC1 reduces the leukocyte-dependent myocardial damage associated with an ischemia-reperfusion procedure.     

Matching diatom assemblages in lake sediment cores and modern surface sediment samples: the implications for lake conservation and restoration with special reference to acidified systems

Restoration goals for damaged freshwater habitats can bedefinedaccording to ecological as well as to chemical criteria. Fordisturbed lakes, the sediment microfossil record can be usedtoselect potential modern analogue sites as possible restorationtarget ecosystems.Fossil diatom assemblages in two acidified lakes (Round LochofGlenhead and Loch Dee) in Galloway, Scotland, were comparedfloristically with modern surface sediment samples from ca. 200lakes in Britain, Ireland, Sweden and Norway using numericaltechniques. Mean squared Chi-squared dissimilarity (SCD)valuesbased on between sample Chi-square distance measures were usedtocompare samples.Space-for-time substitution using diatom assemblage matchingtechniques identified several modern analogue sites withHebrideanLoch Teanga and Irish Lough Claggan possessing modern diatomflorasmost similar to those which existed at the Round Loch ofGlenheadand Loch Dee before acidification.From the point of view of atmospheric pollution, the mostcloselymatching modern analogue sites were not necessarily in themostpristine regions. Some analogues occurred in UK regions ofmoderateor low acid deposition and modern diatom assemblages inatmospherically cleaner mid Norway were generally less similarfloristically.It is argued that identification of modern analogue sitesraisesthe possibility of using time-space substitution of closelymatchedmodern and fossil samples to infer whole lake ecosystems.Diatoms are however poor indicators of some water chemistryvariables and the two closest matched modern analogue siteshavetoo high calcium concentrations making faunistic comparisonsquestionable.Identification of good modern analogue lakes can be improvedbyusing selection criteria, other than diatoms, to pre-selectsites.Screening inappropriate sites according to water chemistry andbasin features combined with a larger biological database ofmodernand fossil samples offers a promising way of refining theselectionprocesses.Despite necessary refinements, modern analogue matching canpotentially identify whole lake ecosystems that can serve asbiological target communities for currently disturbed sites.Beingbased on biological rather than chemical criteria, thisapproachdoes not rely on species-water chemistry transfer functions.It istherefore directly relevant to lake conservation andrestorationobjectives and offers an alternative method for reconstructing lakepalaeo-environments.     

An Update on the Functional Molecular Immunology (FIMM) Database

Data on the major histocompatibility complex, T-cell epitopes, B-cell epitopes, antigens and diseases are heterogeneous and scattered among different databases and the literature. Since it has become increasingly difficult to obtain an integrated view of functional immune response components, we have developed and updated over several years the Functional molecular IMMunology (FIMM) database (http:// research.i2r.a-star.edu.sg/fimm/). FIMM contains integrated expert-curated data on protein antigens, and on human immunological receptors that recognise and bind them in healthy or disease states. Interfaces with multiple, intuitive query options and query reports provide immunologists with prioritised information that aids data interpretation, vaccine target discovery and immune disease research.     

富含多糖草莓果实总RNA提取方法的改进

以草莓果实为模式实验材料,将Chomczynski提出的常规RNA提取方法与Kenneth等提出的改进方法相结合,并做了进一步改进,建立了一种简单实用的从富舍多糖的植物材料中提取总RNA的方法。先利用冷的丙酮去除色素类物质,再利用乙二醇丁醚去除多糖,从而有效克服了从富含色素和多糖娄物质的植物材料中提取RNA的困难;获取的RNA样品在纯度和浓度上都可以满足PCR及Northern杂交等分子生物学实验的要求。     

Evidence for the presence and location of annexins in human platelets.

In this study the identity of annexins in human platelets has been determined together with their ability to be released by agents which induce platelet degranulation. The presence of proteins cross-reacting to antibodies against annexins I and V was detected in human platelets. However, the study provided evidence that these annexins are not located on the surface of the plasma membrane in a Ca++ dependent manner. Moreover, activation of platelets with several agents which induced platelet degranulation did not cause release of annexins I or V as determined by both immunoblotting and ELISA.     

The relationship between diatoms and surface water quality in the Høylandet area of Nord-Trøndelag, Norway

Although the ecological effects of surface wateracidification are now well researched, factorscontrolling the abundance and occurrence of aquaticorganisms in unpolluted acid-sensitive systems arepoorly known. The Høylandet region in central Norwayexperiences relatively low levels of atmosphericpollution and its surface waters, although acid, arenot significantly acidified. Hence lakes and streamsin this region were selected to study the influence ofwater chemistry on diatom algae. Relationships betweenthe two were explored using the multivariate techniqueof canonical correspondence analysis (CCA). Theprincipal water chemistry variables influencingspecies composition of periphytic diatoms were foundto be pH and water colour. Furthermore, therelationship between species abundance and pH wassufficiently strong to enable reconstruction of wateracidity from diatom data. Establishing the nature ofaquatic communities in atmospherically clean butgeologically sensitive regions is an important meansof identifying control systems against which therecovery of acidified lakes in polluted regions can beassessed. The Høylandet region has the potential toprovide a Europe-wide control system of this naturebut much further work is required to follow up andextend the results of this preliminary study.     

Characterization of the genome of feline foamy virus and its proteins shows distinct features different from those of primate spumaviruses.

The genome of the feline foamy virus (FeFV) isolate FUV was characterized by molecular cloning and nucleotide sequence analysis of subgenomic proviral DNA. The overall genetic organization of FeFV and protein sequence comparisons of different FeFV genes with their counterparts from other known foamy viruses confirm that FeFV is a complex foamy virus. However, significant differences exist when FeFV is compared with primate foamy viruses. The FeFV Gag protein is smaller than that of the primate spumaviruses, mainly due to additional MA/CA sequences characteristic of the primate viruses only. Gag protein sequence motifs of the NC domain of primate foamy viruses assumed to be involved in genome encapsidation are not conserved in FeFV. FeFV Gag and Pol proteins were detected with monospecific antisera directed against Gag and Pol domains of the human foamy virus and with antisera from naturally infected cats. Proteolytic processing of the FeFV Gag precursor was incomplete, whereas more efficient proteolytic cleavage of the pre125Pro-Pol protein was observed. The active center of the FeFV protease contains a Gln that replaces an invariant Gly residue at this position in other retroviral proteases. Functional studies on FeFV gene expression directed by the promoter of the long terminal repeat showed that FeFV gene expression was strongly activated by the Bell/Tas transactivator protein. The FeFV Bell/Tas transactivator is about one-third smaller than its counterpart of primate spumaviruses. This difference is also reflected by a limited sequence similarity and only a moderate conservation of structural motifs of the different foamy virus transactivators analyzed.