Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 6 de 6
Filter
Add more filters










Database
Language
Publication year range
1.
Am J Physiol Heart Circ Physiol ; 311(6): H1392-H1408, 2016 12 01.
Article in English | MEDLINE | ID: mdl-27694217

ABSTRACT

The HDL receptor SR-BI mediates the transfer of cholesteryl esters from HDL to cells and controls HDL abundance and structure. Depending on the genetic background, loss of SR-BI causes hypercholesterolemia, anemia, reticulocytosis, splenomegaly, thrombocytopenia, female infertility, and fatal coronary heart disease (CHD). The carboxy terminus of SR-BI (505QEAKL509) must bind to the cytoplasmic adaptor PDZK1 for normal hepatic-but not steroidogenic cell-expression of SR-BI protein. To determine whether SR-BI's carboxy terminus is also required for normal protein levels in steroidogenic cells, we introduced into SR-BI's gene a 507Ala/STOP mutation that produces a truncated receptor (SR-BIΔCT). As expected, the dramatic reduction of hepatic receptor protein in SR-BIΔCT mice was similar to that in PDZK1 knockout (KO) mice. Unlike SR-BI KO females, SR-BIΔCT females were fertile. The severity of SR-BIΔCT mice's hypercholesterolemia was intermediate between those of SR-BI KO and PDZK1 KO mice. Substantially reduced levels of the receptor in adrenal cortical cells, ovarian cells, and testicular Leydig cells in SR-BIΔCT mice suggested that steroidogenic cells have an adaptor(s) functionally analogous to hepatic PDZK1. When SR-BIΔCT mice were crossed with apolipoprotein E KO mice (SR-BIΔCT/apoE KO), pathologies including hypercholesterolemia, macrocytic anemia, hepatic and splenic extramedullary hematopoiesis, massive splenomegaly, reticulocytosis, thrombocytopenia, and rapid-onset and fatal occlusive coronary arterial atherosclerosis and CHD (median age of death: 9 wk) were observed. These results provide new insights into the control of SR-BI in steroidogenic cells and establish SR-BIΔCT/apoE KO mice as a new animal model for the study of CHD.


Subject(s)
Adrenal Cortex/metabolism , Hypercholesterolemia/genetics , Leydig Cells/metabolism , Liver/metabolism , Ovary/metabolism , Scavenger Receptors, Class B/genetics , Anemia, Macrocytic/genetics , Animals , Apolipoproteins E/genetics , Coronary Artery Disease/genetics , Coronary Artery Disease/mortality , Coronary Disease/genetics , Coronary Disease/mortality , Coronary Occlusion/genetics , Coronary Occlusion/mortality , Female , Gene Knock-In Techniques , Hematopoiesis, Extramedullary/genetics , Immunoblotting , Lipoproteins, HDL/genetics , Male , Mice , Mutation , Polymerase Chain Reaction , Receptors, Lipoprotein/genetics , Reticulocytosis/genetics , Splenomegaly/genetics , Thrombocytopenia/genetics , Transcriptome
2.
Clin Chim Acta ; 442: 125-9, 2015 Mar 10.
Article in English | MEDLINE | ID: mdl-25632835

ABSTRACT

BACKGROUND: Misdiagnosis of G-6-PD deficiency in neonates, at risk of severe hemolytic episodes, extreme hyperbilirubinemia, and bilirubin encephalopathy, could possibly occur due to presence of reticulocytes, which contain higher amounts of G-6-PD than mature erythrocytes. G-6-PD mutations in the population might also affect G-6-PD activity. This study evaluated the relationship among G-6-PD activity, G-6-PD variants and reticulocytosis in northeastern Thai neonates. METHODS: Blood samples obtained from routine fluorescence spot test examination for G-6-PD deficiency were analyzed using a quantitative enzymatic assay and for common G-6-PD mutations by restriction fragment length polymorphism (RFLP)-PCR. Correlation between G-6-PD activity and percent reticulocytosis was determined. RESULTS: Among 106G-6-PD-deficient (G-6PD activity<7.0U/g Hb) neonates, no significant association is observed between G-6PD activity and percent reticulocytosis (r=0.125, p-value=0.201), but there is a weak correlation in G-6-PD-normal neonates (r=0.377, p-value=0.014). There is a high frequency of G-6-PD Viangchan in male hemizygous and female heterozygous G-6-PD-deficient and G-6-PD-normal neonates. CONCLUSIONS: A high reticulocytosis does not bias measurements of enzyme activity in G-6-PD-deficient neonates. Also, G-6-PD activity varies among female heterozygous neonates, and G-6-PD mutation analysis provides a reliable method to detect G-6-PD deficiency.


Subject(s)
Enzyme Assays , Glucosephosphate Dehydrogenase/genetics , Glucosephosphate Dehydrogenase/metabolism , Mutation , Reticulocytosis/genetics , Artifacts , Female , Genotyping Techniques , Glucosephosphate Dehydrogenase/blood , Glucosephosphate Dehydrogenase Deficiency/blood , Glucosephosphate Dehydrogenase Deficiency/enzymology , Glucosephosphate Dehydrogenase Deficiency/genetics , Glucosephosphate Dehydrogenase Deficiency/physiopathology , Humans , Infant, Newborn , Male , Thailand
3.
Blood ; 121(13): 2553-62, 2013 Mar 28.
Article in English | MEDLINE | ID: mdl-23361909

ABSTRACT

B-cell lymphoma 11A (BCL11A) downregulation in human primary adult erythroid progenitors results in elevated expression of fetal γ-globin. Recent reports showed that BCL11A expression is activated by KLF1, leading to γ-globin repression. To study regulation of erythropoiesis and globin expression by KLF1 and BCL11A in an in vivo model, we used mice carrying a human ß-globin locus transgene with combinations of Klf1 knockout, Bcl11a floxed, and EpoR(Cre) knockin alleles. We found a higher percentage of reticulocytes in adult Klf1(wt/ko) mice and a mild compensated anemia in Bcl11a(cko/cko) mice. These phenotypes were more pronounced in compound Klf1(wt/ko)::Bcl11a(cko/cko) mice. Analysis of Klf1(wt/ko), Bcl11a(cko/cko), and Klf1(wt/ko)::Bcl11a(cko/cko) mutant embryos demonstrated increased expression of mouse embryonic globins during fetal development. Expression of human γ-globin remained high in Bcl11a(cko/cko) embryos during fetal development, and this was further augmented in Klf1(wt/ko)::Bcl11a(cko/cko) embryos. After birth, expression of human γ-globin and mouse embryonic globins decreased in Bcl11a(cko/cko) and Klf1(wt/ko)::Bcl11a(cko/cko) mice, but the levels remained much higher than those observed in control animals. Collectively, our data support an important role for the KLF1-BCL11A axis in erythroid maturation and developmental regulation of globin expression.


Subject(s)
Carrier Proteins/genetics , Erythropoiesis/genetics , Genes, Switch/genetics , Globins/genetics , Kruppel-Like Transcription Factors/genetics , Nuclear Proteins/genetics , Animals , DNA-Binding Proteins , Embryo, Mammalian , Erythropoiesis/physiology , Fetal Development/genetics , Gene Expression Regulation, Developmental , Gene Rearrangement/genetics , Gene Rearrangement/physiology , Genes, Switch/physiology , Humans , Mice , Mice, Mutant Strains , Mice, Transgenic , Repressor Proteins , Reticulocytosis/genetics , Reticulocytosis/physiology , Spleen/cytology , Spleen/embryology , Spleen/metabolism
4.
Blood Cells Mol Dis ; 48(3): 173-8, 2012 Mar 15.
Article in English | MEDLINE | ID: mdl-22244935

ABSTRACT

Cell surface proteins Hfe, Tfr2, hemojuvelin and Tmprss6 play key roles in iron homeostasis. Hfe and Tfr2 induce transcription of hepcidin, a small peptide that promotes the degradation of the iron transporter ferroportin. Hemojuvelin, a co-receptor for bone morphogenic proteins, induces hepcidin transcription through a Smad signaling pathway. Tmprss6 (also known as matriptase-2), a membrane serine protease that has been found to bind and degrade hemojuvelin in vitro, is a potent suppressor of hepcidin expression. In order to examine if Hfe and Tfr2 are substrates for Tmprss6, we generated mice lacking functional Hfe or Tfr2 and Tmprss6. We found that double mutant mice lacking functional Hfe or Tfr2 and Tmprss6 exhibited a severe iron deficiency microcytic anemia phenotype mimicking the phenotype of single mutant mice lacking functional Tmprss6 (Tmprss6msk/msk mutant) demonstrating that Hfe and Tfr2 are not substrates for Tmprss6. Nevertheless, the phenotype of the mice lacking Hfe or Tfr2 and Tmprss6 differed from Tmprss6 deficient mice alone, in that the double mutant mice exhibited much greater erythropoiesis. Hfe and Tfr2 have been shown to play important roles in the erythron, independent of their role in regulating liver hepcidin transcription. We demonstrate that lack of functional Tfr2 and Hfe allows for increased erythropoiesis even in the presence of high hepcidin expression, but the high levels of hepcidin levels significantly limit the availability of iron to the erythron, resulting in ineffective erythropoiesis. Furthermore, repression of hepcidin expression by hypoxia was unaffected by the loss of functional Hfe, Tfr2 and Tmprss6.


Subject(s)
Anemia, Hypochromic/genetics , Erythropoiesis/genetics , Membrane Proteins/deficiency , Receptors, Transferrin/deficiency , Serine Endopeptidases/deficiency , Anemia, Hypochromic/metabolism , Animals , Erythropoietin/blood , Female , Hemochromatosis Protein , Histocompatibility Antigens Class I/genetics , Hypoxia/genetics , Male , Membrane Proteins/genetics , Mice , Mice, 129 Strain , Mice, Inbred AKR , Mice, Inbred C57BL , Mice, Knockout , Phenotype , Receptors, Transferrin/genetics , Reticulocytosis/genetics , Serine Endopeptidases/genetics
5.
Arterioscler Thromb Vasc Biol ; 30(7): 1439-45, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20431066

ABSTRACT

OBJECTIVE: Disruption of scavenger receptor class B type I (SR-BI) in mice impairs high-density lipoprotein (HDL)-cholesterol (HDL-C) delivery to the liver and induces susceptibility to atherosclerosis. In this study, it was investigated whether introduction of cholesteryl ester transfer protein (CETP) can normalize HDL-C transport to the liver and reduce atherosclerosis in SR-BI knockout (KO) mice. METHODS AND RESULTS: Expression of human CETP in SR-BI(KO) mice resulted in decreased plasma HDL-C levels, both on chow diet (1.8-fold, P<0.001) and on challenge with Western-type diet (1.6-fold, P<0.01). Furthermore, the presence of CETP partially normalized the abnormally large HDL particles observed in SR-BI(KO) mice. Unexpectedly, expression of CETP in SR-BI(KO) mice did not reduce atherosclerotic lesion development, probably because of consequences of SR-BI deficiency, including the persistence of higher VLDL-cholesterol (VLDL-C) levels, unchanged elevated free cholesterol/total cholesterol ratio, and the increased oxidative status of the animals. In addition, CETP expression did not normalize other characteristics of SR-BI deficiency, including female infertility, reticulocytosis, thrombocytopenia, and impaired platelet aggregation. CONCLUSIONS: CETP restores HDL-C levels in SR-BI(KO) mice, but it does not change the susceptibility to atherosclerosis and other typical characteristics that are associated with SR-BI disruption. This may indicate that the pathophysiology of SR-BI deficiency is not a direct consequence of changes in the HDL pool.


Subject(s)
Atherosclerosis/metabolism , Cholesterol Ester Transfer Proteins/metabolism , Cholesterol, HDL/blood , Liver/metabolism , Scavenger Receptors, Class B/deficiency , Animals , Atherosclerosis/genetics , Atherosclerosis/pathology , Cholesterol Ester Transfer Proteins/genetics , Cholesterol, LDL/blood , Cholesterol, VLDL/blood , Disease Models, Animal , Female , Humans , Infertility, Female/genetics , Infertility, Female/metabolism , Kinetics , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Mice, Transgenic , Oxidative Stress , Particle Size , Platelet Aggregation/genetics , Platelet Count , Reticulocytosis/genetics , Scavenger Receptors, Class B/genetics
6.
Blood ; 108(12): 3637-45, 2006 Dec 01.
Article in English | MEDLINE | ID: mdl-16882712

ABSTRACT

Actin oligomers are a significant structural component of the erythrocyte cytoskeleton. Rac1 and Rac2 GTPases regulate actin structures and have multiple overlapping as well as distinct roles in hematopoietic cells; therefore, we studied their role in red blood cells (RBCs). Conditional gene targeting with a loxP-flanked Rac1 gene allowed Crerecombinase-induced deletion of Rac1 on a Rac2 null genetic background. The Rac1(-/-);Rac2(-/-) mice developed microcytic anemia with a hemoglobin drop of about 20% and significant anisocytosis and poikilocytosis. Reticulocytes increased more than 2-fold. Rac1(-/-);Rac2(-/-) RBCs stained with rhodamine-phalloidin demonstrated F-actin meshwork gaps and aggregates under confocal microscopy. Transmission electron microscopy of the cytoskeleton demonstrated junctional aggregates and pronounced irregularity of the hexagonal spectrin scaffold. Ektacytometry confirmed that these cytoskeletal changes in Rac1(-/-);Rac2(-/-) erythrocytes were associated with significantly decreased cellular deformability. The composition of the cytoskeletal proteins was altered with an increased actin-to-spectrin ratio and increased phosphorylation (Ser724) of adducin, an F-actin capping protein. Actin and phosphorylated adducin of Rac1(-/-);Rac2(-/-) erythrocytes were more easily extractable by Triton X-100, indicating weaker association to the cytoskeleton. Thus, deficiency of Rac1 and Rac2 GTPases in mice alters actin assembly in RBCs and causes microcytic anemia with reticulocytosis, implicating Rac GTPases as dynamic regulators of the erythrocyte cytoskeleton organization.


Subject(s)
Actin Cytoskeleton/metabolism , Erythrocyte Membrane/metabolism , Neuropeptides/metabolism , Reticulocytes/metabolism , rac GTP-Binding Proteins/metabolism , Actin Cytoskeleton/genetics , Anemia/genetics , Anemia/metabolism , Anemia/pathology , Animals , Calmodulin-Binding Proteins/metabolism , Carrier Proteins/metabolism , Erythrocyte Membrane/genetics , Erythrocyte Membrane/ultrastructure , Mice , Mice, Knockout , Microfilament Proteins/metabolism , Neuropeptides/deficiency , Phosphorylation , Protein Processing, Post-Translational/genetics , Reticulocytes/ultrastructure , Reticulocytosis/genetics , Spectrin/metabolism , rac GTP-Binding Proteins/deficiency , rac1 GTP-Binding Protein , RAC2 GTP-Binding Protein
SELECTION OF CITATIONS
SEARCH DETAIL
...