101 research outputs found

    Impact of climate induced glacial melting on coastal marine systems in the Western Antarctic Peninsula region

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    IMCOAST is an international research program that features a multidisciplinary approach involving geo and biological sciences, field investigations, remote sensing and modeling and knowledge into the hydrographical and biological history of the marine coastal ecosystems of the Western Antarctic Peninsula region

    State and Transition Model of Lowland Grassland in Flooding Pampa

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    Rainfall conditions are considered to be a major factor in determining vegetation structure in temperate grasslands with grazing playing a secondary role (Biondini et al., 1998; Sternberg et al., 2000). In order to analyse the relative importance of both factors on the lowland community of the Flooding Pampa we compared the responses of functional groups under both intermittent and continuous grazing regimes over a 3- year period of important inter seasonal rainfall variation. The results are presented in a state and transition model

    Grassland Use and Plant Diversity in Grazed Ecosystems

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    Earth biomes are being deconstructed, through unprecedented rates of species disappearance or invasion (McCann 2000). This, added to the threat of global environmental change and changes in values of a developed society, caused that biodiversity became a topic that has captured the attention of the public as well as the scientific community. Such concern on the importance of biodiversity is based in four basic reasons clearly described by West (1993): (i) morality, that aims for the protection of species; (ii) aesthetics, as people desire to see and appreciate the living parts of nature; (iii) economics and, (iv) the array of “services” provided by the natural ecosystems. It is vital to know how badly is affecting ecosystem function human alarming rate of destroying the original diversity

    Analysis of Some Farm Driving Variables and Its Relation with Milk Production in a Pastoral Dairy Farm of Buenos Aires, Argentina

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    The quantity of milk solids produced determines a dairy farm income and contributes to its profit. Total pasture production, forage quality and herd consumption are factors to be managed in this production system. The outcomes of two years were analyzed. Primary production showed its dependence on climatic conditions and use of technological inputs. Forage quality was promoted through interseeding legumes, applying fertilizer and maintaining the pasture young and leafy. Total forage removed by the herd was similar in both years although pasture production decreased. It was possible to cope with seasonal variations in forage production, by varying the grazing pressure and this allowed an increase in daily herd milk production and annual fat production per hectare. Changes in milk production per cow was not related to changes in stocking rate, however, although the nutritive value of the pasture was improved during the second period, daily milk production and forage consumption per animal decreased when grazing pressure increased. The relation between total milk produced and total dry matter consumed in both periods were similar

    The Effect of Phosphorus Fertilization on Botanical Composition and Production in Temperate Pastures in Argentina

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    The objective of this paper is to evaluate floristic changes and above-ground primary production in native grasslands and old pastures dominated by tall fescue (Festuca arundinacea) that were fertilized with different levels of phosphorus. For this, aerial biomass was sequentially harvested from November 1998 to October 1999. Above-ground production of native grassland more than doubled (from 3000 to 7300 kg DM/ha) with the highest level of P through the increment of three naturalized species: the winter annual ryegrass (Lolium multiflorum) and two legumes: white clover (Trifolium repens) and lotus (Lotus corniculatus). In contrast, above-ground production of old fescue pastures remained unchanged while nutritive value improved as legumes and warm-season grasses increased where they were fertilized

    The Expression of CD154 by Kaposi's Sarcoma Cells Mediates the Anti-Apoptotic and Migratory Effects of HIV-1-Tat Protein:

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    Kaposi's sarcoma (KS) is a malignancy associated to conditions of immune system impairment such as HIV-1 infection and post-transplantation therapy. Here we report that HIV-1-Tat protein, at concentrations well below those detected in AIDS patients, up-regulates the expression of both CD40 and CD154 on KS cells. This occurred also in the presence of vincristine, that at doses shown to induce apoptosis decreased the expression of both CD40 and CD154 on KS cells. The treatment with a soluble CD40-muIg fusion protein (CD40 fp) that prevents the binding of CD154 with cell surface CD40, as well as the transfection with a vector for soluble CD40 (KS sCD40), decreased the anti-apoptotic effect of Tat. Moreover, Tat-induced motility of KS cells was inhibited by soluble CD40 fp. Tat also enhanced the expression of intracellular proteins known to transduce signals triggered by CD40 engagement, in particular TRAF-3. Tat as well as soluble CD154 (sCD154) prevented vincristine-induced reduction of TRAF-3 in KS cells t..

    Human liver stem cell-derived microvesicles accelerate hepatic regeneration in hepatectomized rats

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    Several studies indicate that adult stem cells may improve the recovery from acute tissue injury. It has been suggested that they may contribute to tissue regeneration by the release of paracrine factors promoting proliferation of tissue resident cells. However, the factors involved remain unknown. In the present study we found that microvesicles (MVs) derived from human liver stem cells (HLSC) induced in vitro proliferation and apoptosis resistance of human and rat hepatocytes. These effects required internalization of MVs in the hepatocytes by an α4-integrin-dependent mechanism. However, MVs pre-treated with RNase, even if internalized, were unable to induce hepatocyte proliferation and apoptosis resistance, suggesting an RNA-dependent effect. Microarray analysis and quantitative RT-PCR demonstrated that MVs were shuttling a specific subset of cellular mRNA, such as mRNA associated in the control of transcription, translation, proliferation and apoptosis. When administered in vivo, MVs accelerated the morphological and functional recovery of liver in a model of 70% hepatectomy in rats. This effect was associated with increase in hepatocyte proliferation and was abolished by RNase pre-treatment of MVs. Using human AGO2, as a reporter gene present in MVs, we found the expression of human AGO2 mRNA and protein in the liver of hepatectomized rats treated with MVs. These data suggested a translation of the MV shuttled mRNA into hepatocytes of treated rats. In conclusion, these results suggest that MVs derived from HLSC may activate a proliferative program in remnant hepatocytes after hepatectomy by a horizontal transfer of specific mRNA subsets

    Microparticle-mediated transfer of the viral receptors CAR and CD46, and the CFTR channel in a CHO cell model confers new functions to target cells

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    Cell microparticles (MPs) released in the extracellular milieu can embark plasma membrane and intracellular components which are specific of their cellular origin, and transfer them to target cells. The MP-mediated, cell-to-cell transfer of three human membrane glycoproteins of different degrees of complexity was investigated in the present study, using a CHO cell model system. We first tested the delivery of CAR and CD46, two monospanins which act as adenovirus receptors, to target CHO cells. CHO cells lack CAR and CD46, high affinity receptors for human adenovirus serotype 5 (HAdV5), and serotype 35 (HAdV35), respectively. We found that MPs derived from CHO cells (MP-donor cells) constitutively expressing CAR (MP-CAR) or CD46 (MP-CD46) were able to transfer CAR and CD46 to target CHO cells, and conferred selective permissiveness to HAdV5 and HAdV35. In addition, target CHO cells incubated with MP-CD46 acquired the CD46-associated function in complement regulation. We also explored the MP-mediated delivery of a dodecaspanin membrane glycoprotein, the CFTR to target CHO cells. CFTR functions as a chloride channel in human cells and is implicated in the genetic disease cystic fibrosis. Target CHO cells incubated with MPs produced by CHO cells constitutively expressing GFP-tagged CFTR (MP-GFP-CFTR) were found to gain a new cellular function, the chloride channel activity associated to CFTR. Time-course analysis of the appearance of GFP-CFTR in target cells suggested that MPs could achieve the delivery of CFTR to target cells via two mechanisms: the transfer of mature, membrane-inserted CFTR glycoprotein, and the transfer of CFTR-encoding mRNA. These results confirmed that cell-derived MPs represent a new class of promising therapeutic vehicles for the delivery of bioactive macromolecules, proteins or mRNAs, the latter exerting the desired therapeutic effect in target cells via de novo synthesis of their encoded proteins

    Microvesicles Derived from Mesenchymal Stem Cells Enhance Survival in a Lethal Model of Acute Kidney Injury

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    Several studies demonstrated that treatment with mesenchymal stem cells (MSCs) reduces cisplatin mortality in mice. Microvesicles (MVs) released from MSCs were previously shown to favor renal repair in non lethal toxic and ischemic acute renal injury (AKI). In the present study we investigated the effects of MSC-derived MVs in SCID mice survival in lethal cisplatin-induced AKI. Moreover, we evaluated in vitro the effect of MVs on cisplatin-induced apoptosis of human renal tubular epithelial cells and the molecular mechanisms involved. Two different regimens of MV injection were used. The single administration of MVs ameliorated renal function and morphology, and improved survival but did not prevent chronic tubular injury and persistent increase in BUN and creatinine. Multiple injections of MVs further decreased mortality and at day 21 surviving mice showed normal histology and renal function. The mechanism of protection was mainly ascribed to an anti-apoptotic effect of MVs. In vitro studies demonstrated that MVs up-regulated in cisplatin-treated human tubular epithelial cells anti-apoptotic genes, such as Bcl-xL, Bcl2 and BIRC8 and down-regulated genes that have a central role in the execution-phase of cell apoptosis such as Casp1, Casp8 and LTA. In conclusion, MVs released from MSCs were found to exert a pro-survival effect on renal cells in vitro and in vivo, suggesting that MVs may contribute to renal protection conferred by MSCs
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