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      MECANISMO MOLECULAR DE LAS ESTATINAS EN EL TRATAMIENTO DE LA ERITROCITOSIS PATOLÓGICA DE ALTURA Translated title: MOLECULAR MECHANISM OF STATINS IN THE TREATMENT OF HIGH ALTITUDE PATHOLOGICAL ERYTHROCYTOSIS

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          Abstract

          Introducción La Eritrocitosis Patológica de Altura es la manifestación hematológica de la Enfermedad Crónica de Altura, por adaptación inadecuada a grandes alturas de genes reguladores de la eritropoyesis. Las estatinas son inhibidores de la vía del mevalonato involucrado en la regulación de la eritropoyesis. El presente trabajo describe los mecanismos moleculares de la inhibición de la eritropoyesis en pacientes con eritrocitosis patológicas. Material y métodos Se estudiaron 35 pacientes con eritrocitosis patológicas con radicatorias en las ciudades de La Paz y El Alto (3600 y 4000 msnm respectivamente). Se realizaron Cultivo de células progenitoras hematopoyéticas y Western Blot. Resultados Statins induce apoptosis of erythroid progenitors in the cell culture medium. Without the supplement of simvastatin the apoptosis was 12.3% and With simvastatin the apoptosis was 38.4% (p = 0.001). Furthermore statins inhibit the proliferation and differentiation of erythroid progenitors. Conclusiones Los mecanismos moleculares involucrados en la inhibición de la eritropoyesis son: a) Bloqueo de la isoprenilación de Rho y Ras, b) Inhibición de la fosforilación de Jak-2 y Stat-5, c) inhibición de la glicosilación del EpoR, d) Disminución de colesterol en microdominios de la membrana celular (raft lipid), e) Inducción de apoptosis a través de BCLxL y caspasa 9.

          Translated abstract

          Introduction The High altitude Pathological Erythrocytosis is the chronic mountain sickness hematologic manifestation by inadequate adaptation to high altitudes of genes regulating erythropoiesis. Statins are inhibitors of the mevalonate pathway involved in the regulation of erythropoiesis. This paper describes the molecular mechanisms of erythropoiesis inhibitionin patients with pathological erythrocytosis. Material and methods We studied 35 patients with pathological erythrocytosis from La Paz and El Alto city (3600 and 4000 masl respectively). Were performed hematopoietic progenitor cell culture and Western blotting. Results Statins induce apoptosis in liquid culture medium. without simvastatin erythroid progenitors from apoptosis presentarón and 12.3% in the group supplemented with simvastatin 38.4% apoptosis (p = 0.001), statins also inhibit the proliferation and differentiation of erythroid progenitors, and inhibit transcription of STAT-5. Conclusions The molecular mechanisms involved in the erythropoiesis inhibition are: a) Inhibition of Ras and Rho isoprenylation, b) Inhibition of Jak-2 and Stat-5 phosphorylation, c) inhibition of EpoR glycosylation, d) Statins reduce lipid rafts cholesterol and reduce JAK2 localization to lipid rafts, e) Induction of apoptosis through caspase 9 and BclxL.

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          Most cited references28

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          Lipid raft microdomains and neurotransmitter signalling.

          Lipid rafts are specialized structures on the plasma membrane that have an altered lipid composition as well as links to the cytoskeleton. It has been proposed that these structures are membrane domains in which neurotransmitter signalling might occur through a clustering of receptors and components of receptor-activated signalling cascades. The localization of these proteins in lipid rafts, which is affected by the cytoskeleton, also influences the potency and efficacy of neurotransmitter receptors and transporters. The effect of lipid rafts on neurotransmitter signalling has also been implicated in neurological and psychiatric diseases.
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            Erythropoiesis: development and differentiation.

            Through their oxygen delivery function, red blood cells are pivotal to the healthy existence of all vertebrate organisms. These cells are required during all stages of life--embryonic, fetal, neonatal, adolescent, and adult. In the adult, red blood cells are the terminally differentiated end-product cells of a complex hierarchy of hematopoietic progenitors that become progressively restricted to the erythroid lineage. During this stepwise differentiation process, erythroid progenitors undergo enormous expansion, so as to fulfill the daily requirement of ~2 × 10(11) new erythrocytes. How the erythroid lineage is made has been a topic of intense research over the last decades. Developmental studies show that there are two types of red blood cells--embryonic and adult. They develop from distinct hemogenic/hematopoietic progenitors in different anatomical sites and show distinct genetic programs. This article highlights the developmental and differentiation events necessary in the production of hemoglobin-producing red blood cells.
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              Apoptotic mechanisms in the control of erythropoiesis.

              U Testa (2004)
              Erythropoiesis is a complex multistep process encompassing the differentiation of hemopoietic stem cells to mature erythrocytes. The steps involved in this complex differentiation process are numerous and involve first the differentiation to early erythoid progenitors (burst-forming units-erythroid, BFU-E), then to late erythroid progenitors (colony-forming units-erythroid) and finally to morphologically recognizable erythroid precursors. A key event of late stages of erythropoiesis is nuclear condensation, followed by extrusion of the nucleus to produce enucleated reticulocytes and finally mature erythrocytes. During the differentiation process, the cells became progressively sensitive to erythropoietin that controls both the survival and proliferation of erythroid cells. A normal homeostasis of the erythropoietic system requires an appropriate balance between the rate of erythroid cell production and red blood cell destruction. Growing evidences outlined in the present review indicate that apoptotic mechanism play a relevant role in the control of erythropoiesis under physiologic and pathologic conditions. Withdrawal of erythropoietin or stimulation of death receptors such as Fas or TRAIL-Rs leads to activation of a subset of caspase-3, -7 and -8, which then cleave the transcription factors GATA-1 and TAL-1 and trigger apoptosis. In addition, there is evidence that a number of caspases are physiologically activated during erythroid differentiation and are functionally required for erythroid maturation. Several caspase substrates are cleaved in differentiating cells, including the protein acinus whose activation by cleavage is required for chromatin condensation. The studies on normal erythropoiesis have clearly indicated that immature erythroid precursors are sensitive to apoptotic triggering mediated by activation of the intrinsic and extrinsic apoptotic pathways. These apoptotic mechanisms are frequently exacerbated in some pathologic conditions, associated with the development of anemia (ie, thalassemias, multiple myeloma, myelodysplasia, aplastic anemia). The considerable progress in our understanding of the apoptotic mechanisms underlying normal and pathologic erythropoiesis may offer the way to improve the treatment of several pathologic conditions associated with the development of anemia.
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                Author and article information

                Contributors
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Journal
                rmcmlp
                Revista Médica La Paz
                Rev. Méd. La Paz
                Colegio Médico de La Paz (La Paz, , Bolivia )
                1726-8958
                December 2013
                : 19
                : 2
                : 19-27
                Affiliations
                [01] La Paz orgnameUniversidad Mayor de San Andrés orgdiv1Facultad de Medicina orgdiv2Departamento de Ciencias Funcionales Bolivia amaru.ricardo@ 123456icloud.com
                Article
                S1726-89582013000200003
                b184f6d2-74b6-43ef-a961-30af07c58cd8

                This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

                History
                : 02 July 2013
                : 07 August 2013
                Page count
                Figures: 0, Tables: 0, Equations: 0, References: 19, Pages: 9
                Product

                SciELO Bolivia


                Eritrocitosis patológica de altura,enfermedad crónica de altura,estatinas,Pathological Erythrocytosis,Chronic mountain sickness,statins

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