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      El factor de crecimiento del endotelio vascular hepático en la infección murina por Schistosoma mansoni Translated title: The endothelial growth factor vascular infection in murine liver by Schistosoma mansoni

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          Abstract

          Los antígenos secretados por los huevos de S. mansoni inducen la proliferación de células endoteliales in vivo, así como la producción del Factor de Crecimiento del Endotelio Vascular (VEGF), sugiriendo que la patogénesis en la esquistosomiasis se relaciona con eventos angiogénicos. Se evaluó la expresión del VEGF, como una medida de angiogénesis estimulada por los huevos y los gusanos de S. mansoni, en la infección Bisexual (BIS) y los gusanos adulto (infección UNI) en el hígado de ratones Balb/c, antes y después del tratamiento con PZQ. Los resultados indican que tanto la infección UNI como BIS son capaces de estimular la producción de VEGF en tejido hepático, lo que explica la vascularizacón anómala durante este cuadro infeccioso. Este proceso se acompaña con la presencia de un elevado número de infiltrados leucocitarios en los sitios donde se observa lesión tisular; la producción de VEFG remite tras 48 de tratamiento con PZQ. Estos resultados indican que la producción anómala de VEGF junto con la intensa respuesta pro-inflamatoria asociada no solo a la actividad de VEGF sino también a los infiltrados leucocitarios observados en el tejido hepático, causada tanto por los huevos secretados como por las formas adultas de S. mansoni son los mecanismos que subyacen a las lesiones granulomatosas observadas durante el curso de la esquistosomiasis, pudiendo al menos revertirse el incremento en la vascularización mediante el uso de PZQ.

          Translated abstract

          The antigens secreted by eggs of S. mansoni induce the proliferation of endothelial cells in vivo, as well as the production of Factor Vascular Endothelial Growth factor (VEGF), suggesting that the pathogenesis of schistosomiasis relations with angiogenic events. We evaluated the expression of VEGF, as a measure of angiogenesis stimulated by the eggs and worms S. mansoni in infection bisexual (BIS) and adult worms ( UNI infection ) in the liver of BALB / c mice before and after treatment with PZQ. These results indicate that abnormal production of VEGF with intense pro-inflammatory response not only associated with the activity of VEGF but also leukocyte infiltrates observed in the liver tissue caused by both secreted and eggs by adult forms S. mansoni are the mechanisms underlying granulomatous lesions observed during the course of schistosomiasis, and can be reversed at least the increased vascularization by using PZQ .

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          Most cited references32

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          Heterozygous embryonic lethality induced by targeted inactivation of the VEGF gene.

          Angiogenesis is required for a wide variety of physiological and pathological processes. The endothelial cell-specific mitogen vascular endothelial growth factor (VEGF) is a major mediator of pathological angiogenesis. Also, the expression of VEGF and its two receptors, Flt-1 and Flk-1/KDR, is related to the formation of blood vessels in mouse and rat embryos. Mice homozygous for mutations that inactivate either receptor die in utero between days 8.5 and 9.5. However, ligand(s) other than VEGF might activate such receptors. To assess the role of VEGF directly, we disrupted the VEGF gene in embryonic stem cells. Here we report the unexpected finding that loss of a single VEGF allele is lethal in the mouse embryo between days 11 and 12. Angiogenesis and blood-island formation were impaired, resulting in several developmental anomalies. Furthermore, VEGF-null embryonic stem cells exhibit a dramatically reduced ability to form tumours in nude mice.
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            Proinflammatory Role of Vascular Endothelial Growth Factor in the Pathogenesis of Rheumatoid Arthritis: Prospects for Therapeutic Intervention

            Recent experimental and clinical studies have placed new emphasis on the role of angiogenesis in chronic inflammatory disease. Vascular endothelial growth factor (VEGF) and its receptors are the best characterized system in the regulation of rheumatoid arthritis (RA) by angiogenesis. Furthermore, in addition to its angiogenic role, VEGF can act as a direct proinflammatory mediator during the pathogenesis of RA, and protect rheumatoid synoviocytes from apoptosis, which contributes to synovial hyperplasia. Therefore, the developments of synovial inflammation, hyperplasia, and angiogenesis in the joints of RA patients seem to be regulated by a common cue, namely, VEGF. Agents that target VEGF, such as anti-VEGF antibody and aptamer, have yielded promising clinical data in patients with cancer or macular degeneration, and in RA patients, pharmacologic modulations targeting VEGF or its receptor may offer new therapeutic approaches. In this review, the authors integrate current knowledge of VEGF signaling and information on VEGF antagonists gleaned experimentally and place emphasis on the use of synthetic anti-VEGF hexapeptide to prevent VEGF interacting with its receptor.
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              Role of resident liver cells in the pathogenesis of schistosomiasis.

              Pathology in schistosomiasis occurs as a result of eggs deposited in the liver by the schistosome parasite. A granulomatous reaction occurs, resulting in portal hypertension and hepatic fibrosis. Resident non-parenchymal cells within the liver take part in this process, including hepatic stellate cells, which are responsible for collagen production, and Kupffer cells, the liver macrophages involved in both host protection and in pathology. Other cells such as liver sinusoidal endothelial cells or portal fibroblasts may also be involved in this process. This review discusses the possible role of these resident liver cells in the pathology associated with schistosomiasis and provides information which may assist our understanding of the mechanisms associated with chronic liver disease in general. Copyright © 2012 Elsevier Ltd. All rights reserved.
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                Author and article information

                Journal
                s
                Salus
                Salus
                Universidad de Carabobo (Valencia, Carabobo, Venezuela )
                1316-7138
                December 2013
                : 17
                : 3
                : 27-33
                Affiliations
                [01] Valencia orgnameInstituto de Biología Molecular de Parásitos (Instituto BioMolP) orgdiv1Laboratorio de Helmintología Venezuela
                Article
                S1316-71382013000300005 S1316-7138(13)01700305
                b777fa54-63a2-4b49-94c0-f61bc0f5136b

                http://creativecommons.org/licenses/by/4.0/

                History
                : April 2013
                : September 2013
                Page count
                Figures: 0, Tables: 0, Equations: 0, References: 21, Pages: 7
                Product

                SciELO Venezuela

                Categories
                Artículos

                inflamación crónica,S. mansoni,experimental infection,VEGF,inflammation chronic,infección experimental

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