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Haematologica
2009 Aug 01;948:1049-59. doi: 10.3324/haematol.2008.002873.
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A novel erythroid anion exchange variant (Gly796Arg) of hereditary stomatocytosis associated with dyserythropoiesis.
Iolascon A, De Falco L, Borgese F, Esposito MR, Avvisati RA, Izzo P, Piscopo C, Guizouarn H, Biondani A, Pantaleo A, De Franceschi L.
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Stomatocytoses are a group of inherited autosomal dominant hemolytic anemias and include overhydrated hereditary stomatocytosis, dehydrated hereditary stomatocytosis, hereditary cryohydrocytosis and familial pseudohyperkalemia. We report a novel variant of hereditary stomatocytosis due to a de novo band 3 mutation (p. G796R-band3 CEINGE) associated with a dyserythropoietic phenotype. Band 3 genomic analysis, measurement at of hematologic parameters and red cell indices and morphological analysis of bone marrow were carried out. We then evaluated the red cell membrane permeability and ion transport systems by functional studies of the patient's erythrocytes and Xenopus oocytes transfected with mutated band 3. We analyzed the red cell membrane tyrosine phosphorylation profile and the membrane association of the tyrosine kinases Syk and Lyn from the Src-family-kinase group, since the activity of the membrane cation transport pathways is related to cyclic phosphorylation-dephosphorylation events. The patient showed mild hemolytic anemia with circulating stomatocytes together with signs of dyserythropoiesis. Her red cells displayed increased Na(+) content with decreased K(+)content and abnormal membrane cation transport activities. Functional characterization of band 3 CEINGE in Xenopus oocytes showed that the mutated band 3 is converted from being an anion exchanger (Cl(-), HCO(3)(-)) to being a cation pathway for Na(+) and K(+). Increased tyrosine phosphorylation of some red cell membrane proteins was observed in diseased erythrocytes. Syk and Lyn membrane association was increased in the patient's red cells compared to in normal controls, indicating perturbation of phospho-signaling pathways involved in cell volume regulation events. Band 3 CEINGE alters function from that of anion exchange to cation transport, affects the membrane tyrosine phosphorylation profile, in particular of band 3 and stomatin, and its presence during red cell development likely contributes to dyserythropiesis.
Anong,
Rate of rupture and reattachment of the band 3-ankyrin bridge on the human erythrocyte membrane.
2006, Pubmed
Anong,
Rate of rupture and reattachment of the band 3-ankyrin bridge on the human erythrocyte membrane.
2006,
Pubmed Biondani,
Heat-shock protein-27, -70 and peroxiredoxin-II show molecular chaperone function in sickle red cells: Evidence from transgenic sickle cell mouse model.
2008,
Pubmed Bordin,
Effector-induced Syk-mediated phosphorylation in human erythrocytes.
2005,
Pubmed Bruce,
Red cell membrane transport abnormalities.
2008,
Pubmed Bruce,
Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1.
2005,
Pubmed
,
Xenbase Brugnara,
Regulation of cation content and cell volume in hemoglobin erythrocytes from patients with homozygous hemoglobin C disease.
1985,
Pubmed Brunati,
Sequential phosphorylation of protein band 3 by Syk and Lyn tyrosine kinases in intact human erythrocytes: identification of primary and secondary phosphorylation sites.
2000,
Pubmed Carella,
Genomewide search for dehydrated hereditary stomatocytosis (hereditary xerocytosis): mapping of locus to chromosome 16 (16q23-qter).
1998,
Pubmed Carella,
A second locus mapping to 2q35-36 for familial pseudohyperkalaemia.
2004,
Pubmed Coles,
A variant of hereditary stomatocytosis with marked pseudohyperkalaemia.
1999,
Pubmed De Franceschi,
Membrane cation and anion transport activities in erythrocytes of hereditary spherocytosis: effects of different membrane protein defects.
1997,
Pubmed De Franceschi,
PTPepsilon has a critical role in signaling transduction pathways and phosphoprotein network topology in red cells.
2008,
Pubmed De Franceschi,
Evidence for a protective role of the Gardos channel against hemolysis in murine spherocytosis.
2005,
Pubmed De Franceschi,
Red blood cell cation transports in uraemic anaemia: evidence for an increased K/Cl co-transport activity. Effects of dialysis and erythropoietin treatment.
1995,
Pubmed De Franceschi,
Deficiency of Src family kinases Fgr and Hck results in activation of erythrocyte K/Cl cotransport.
1997,
Pubmed DODGE,
The preparation and chemical characteristics of hemoglobin-free ghosts of human erythrocytes.
1963,
Pubmed Flatt,
The hereditary stomatocytoses.
2009,
Pubmed Glader,
Congenital hemolytic anemia associated with dehydrated erythrocytes and increased potassium loss.
1974,
Pubmed Guizouarn,
Point mutations involved in red cell stomatocytosis convert the electroneutral anion exchanger 1 to a nonselective cation conductance.
2007,
Pubmed
,
Xenbase Harrison,
Phosphorylation of human erythrocyte band 3 by endogenous p72syk.
1994,
Pubmed Jarvis,
A novel stomatocytosis variant showing marked abnormalities in intracellular [Na] and [K] with minimal haemolysis.
2001,
Pubmed Joiner,
Urea stimulation of KCl cotransport induces abnormal volume reduction in sickle reticulocytes.
2007,
Pubmed Li,
Spectrin-level modeling of the cytoskeleton and optical tweezers stretching of the erythrocyte.
2005,
Pubmed Mentzer,
Hereditary stomatocytosis: membrane and metabolism studies.
1975,
Pubmed Miraglia del Giudice,
Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis.
1994,
Pubmed Musch,
Volume expansion stimulates p72(syk) and p56(lyn) in skate erythrocytes.
1999,
Pubmed Musch,
Tyrosine kinase inhibition affects skate anion exchanger isoform I alterations after volume expansion.
2005,
Pubmed Olivieri,
A case of congenital dyserythropoietic anaemia with stomatocytosis, reduced bands 7 and 8 and normal cation content.
1992,
Pubmed Paw,
Cell-specific mitotic defect and dyserythropoiesis associated with erythroid band 3 deficiency.
2003,
Pubmed Perlman,
Cell membrane surface expression and tyrosine kinase regulate the osmolyte channel (skAE1) in skate erythrocytes.
2006,
Pubmed Platt,
Exercise-induced hemolysis in xerocytosis. Erythrocyte dehydration and shear sensitivity.
1981,
Pubmed Rivera,
Effect of complete protein 4.1R deficiency on ion transport properties of murine erythrocytes.
2006,
Pubmed Roncada,
Acrylamide-agarose copolymers: improved resolution of high molecular mass proteins in two-dimensional gel electrophoresis.
2005,
Pubmed Salzer,
Ca(++)-dependent vesicle release from erythrocytes involves stomatin-specific lipid rafts, synexin (annexin VII), and sorcin.
2002,
Pubmed Salzer,
Identification of the phosphorylation site on human erythrocyte band 7 integral membrane protein: implications for a monotopic protein structure.
1993,
Pubmed Stewart,
Hemolytic disease due to membrane ion channel disorders.
2004,
Pubmed Tilly,
Protein tyrosine phosphorylation is involved in osmoregulation of ionic conductances.
1993,
Pubmed Varela,
NAD(P)H oxidase-derived H(2)O(2) signals chloride channel activation in cell volume regulation and cell proliferation.
2004,
Pubmed Walsh,
Transforming growth factor-beta stimulates intestinal epithelial focal adhesion kinase synthesis via Smad- and p38-dependent mechanisms.
2008,
Pubmed