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   <subfield code="a">10.1007/s11010-014-2206-0</subfield>
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   <subfield code="a">Erythropoietin protects red blood cells from TRAIL1-induced cell death during red blood cell transition in Xenopus laevis</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Kei Tamura, Nobuhiko Takamatsu, Michihiko Ito]</subfield>
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   <subfield code="a">In anuran amphibians, larval red blood cells (RBCs) are replaced by adult-type RBCs during metamorphosis. We previously showed that tumor necrosis factor-related apoptosis-inducing ligand 1 (TRAIL1) induces apoptosis in larval-, but not adult-type RBCs in Xenopus laevis. We also found that protein kinase C (PKC) activation is involved in establishing resistance to TRAIL1-induced apoptosis in adult-type RBCs. Here, we investigated whether erythropoietin (EPO), which induces PKC activation in mammalian erythroblasts, is involved in the RBC transition in X. laevis. RT-PCR analysis revealed that epo mRNA was upregulated in the lung, from the metamorphic climax (stage 60) onward. In an RBC culture system, EPO pretreatment significantly attenuated the TRAIL1-induced death of larval- and adult-type RBCs isolated from tadpoles and adults, probably due partly to PKC activation. In samples from froglets undergoing RBC transition, which included both larval- and adult-type RBCs, EPO exhibited a stronger protective effect on the adult-type than the larval-type RBCs. Newly differentiated RBCs isolated from tadpoles treated with a hemolytic reagent were more resistant to TRAIL1-induced cell death than non-treated controls. These results suggest that EPO functions to protect adult-type RBCs from TRAIL1-induced cell death during RBC transition, and that the protective effect might decrease as RBCs age.</subfield>
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   <subfield code="a">Springer Science+Business Media New York, 2014</subfield>
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   <subfield code="a">Red blood cell transition</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Erythropoietin</subfield>
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   <subfield code="a">Protein kinase C</subfield>
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   <subfield code="a">RBC : Red blood cell</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">EPO : Erythropoietin</subfield>
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   <subfield code="a">TRAIL : Tumor necrosis factor-related apoptosis-inducing ligand</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">PKC : Protein kinase C</subfield>
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  <datafield tag="700" ind1="1" ind2=" ">
   <subfield code="a">Tamura</subfield>
   <subfield code="D">Kei</subfield>
   <subfield code="u">Laboratory of Molecular Biology, Department of Biosciences, School of Science, Kitasato University, 1-15-1 Kitasato, Minamiku, 252-0373, Sagamihara, Japan</subfield>
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   <subfield code="a">Takamatsu</subfield>
   <subfield code="D">Nobuhiko</subfield>
   <subfield code="u">Laboratory of Molecular Biology, Department of Biosciences, School of Science, Kitasato University, 1-15-1 Kitasato, Minamiku, 252-0373, Sagamihara, Japan</subfield>
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   <subfield code="a">Ito</subfield>
   <subfield code="D">Michihiko</subfield>
   <subfield code="u">Laboratory of Molecular Biology, Department of Biosciences, School of Science, Kitasato University, 1-15-1 Kitasato, Minamiku, 252-0373, Sagamihara, Japan</subfield>
   <subfield code="4">aut</subfield>
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   <subfield code="t">Molecular and Cellular Biochemistry</subfield>
   <subfield code="d">Springer US; http://www.springer-ny.com</subfield>
   <subfield code="g">398/1-2(2015-01-01), 73-81</subfield>
   <subfield code="x">0300-8177</subfield>
   <subfield code="q">398:1-2&lt;73</subfield>
   <subfield code="1">2015</subfield>
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   <subfield code="a">BK010053</subfield>
   <subfield code="b">XK010053</subfield>
   <subfield code="c">XK010000</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="D">Kei</subfield>
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