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Sandoval H Thiagarajan P Dasgupta SK Schumacher A Prchal JT Chen M Wang J 《Nature》2008,454(7201):232-235
Erythroid cells undergo enucleation and the removal of organelles during terminal differentiation. Although autophagy has been suggested to mediate the elimination of organelles for erythroid maturation, the molecular mechanisms underlying this process remain undefined. Here we report a role for a Bcl-2 family member, Nix (also called Bnip3L), in the regulation of erythroid maturation through mitochondrial autophagy. Nix(-/-) mice developed anaemia with reduced mature erythrocytes and compensatory expansion of erythroid precursors. Erythrocytes in the peripheral blood of Nix(-/-) mice exhibited mitochondrial retention and reduced lifespan in vivo. Although the clearance of ribosomes proceeded normally in the absence of Nix, the entry of mitochondria into autophagosomes for clearance was defective. Deficiency in Nix inhibited the loss of mitochondrial membrane potential (DeltaPsi(m)), and treatment with uncoupling chemicals or a BH3 mimetic induced the loss of DeltaPsi(m) and restored the sequestration of mitochondria into autophagosomes in Nix(-/-) erythroid cells. These results suggest that Nix-dependent loss of DeltaPsi(m) is important for targeting the mitochondria into autophagosomes for clearance during erythroid maturation, and interference with this function impairs erythroid maturation and results in anaemia. Our study may also provide insights into molecular mechanisms underlying mitochondrial quality control involving mitochondrial autophagy. 相似文献
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A common progenitor for human myeloid and lymphoid cells 总被引:15,自引:0,他引:15
J T Prchal D W Throckmorton A J Carroll E W Fuson R A Gams J F Prchal 《Nature》1978,274(5671):590-591
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This paper focuses on combining association measures using corresponding receiver operating characteristic curves. The approach is motivated by a problem of automatic bigram collocation extraction from the field of computational linguistics. It is based on supervised machine learning techniques and the fact that different association measures discover different collocation types. Clusters of equivalent ROC curves are first determined by a testing procedure. The paper’s major contribution is an investigation of the possibility of combining representatives of the clusters of equivalent association measures into more complex models, thus improving performance of the collocation extraction. 相似文献
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Ang SO Chen H Hirota K Gordeuk VR Jelinek J Guan Y Liu E Sergueeva AI Miasnikova GY Mole D Maxwell PH Stockton DW Semenza GL Prchal JT 《Nature genetics》2002,32(4):614-621
Chuvash polycythemia is an autosomal recessive disorder that is endemic to the mid-Volga River region. We previously mapped the locus associated with Chuvash polycythemia to chromosome 3p25. The gene associated with von Hippel-Lindau syndrome, VHL, maps to this region, and homozygosity with respect to a C-->T missense mutation in VHL, causing an arginine-to-tryptophan change at amino-acid residue 200 (Arg200Trp), was identified in all individuals affected with Chuvash polycythemia. The protein VHL modulates the ubiquitination and subsequent destruction of hypoxia-inducible factor 1, subunit alpha (HIF1alpha). Our data indicate that the Arg200Trp substitution impairs the interaction of VHL with HIF1alpha, reducing the rate of degradation of HIF1alpha and resulting in increased expression of downstream target genes including EPO (encoding erythropoietin), SLC2A1 (also known as GLUT1, encoding solute carrier family 2 (facilitated glucose transporter), member 1), TF (encoding transferrin), TFRC (encoding transferrin receptor (p90, CD71)) and VEGF (encoding vascular endothelial growth factor). 相似文献
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