Stomatocytosis is absent in 'stomatin'-deficient murine red blood cells

Blood

Volumn 93, Issue 7, 1999, Pages 2404-2410

  Zhu, Yiwen ^b   Paszty, Chris ^b   Turetsky, Tikva ^b   Tsai, Susan ^b   Kuypers, Frans A ^b   Lee, Gloria ^b   Cooper, Philip ^b   Gallagher, Patrick G ^b   Stevens, Mary E ^b   Rubin, Edward ^b   Mohandas, Narla ^b   Mentzer, William C ^a  

^a SAN FRANCISCO GENERAL HOSPITAL   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

CELL MEMBRANE PROTEIN; MONOVALENT CATION;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CATION TRANSPORT; CELL MEMBRANE PERMEABILITY; CONTROLLED STUDY; ERYTHROCYTE DISORDER; ERYTHROCYTE MEMBRANE; ERYTHROCYTE STRUCTURE; FEMALE; GENE TARGETING; HEMOLYTIC ANEMIA; HOMOZYGOTE; IMMUNOBLOTTING; KNOCKOUT MOUSE; LIPID TRANSPORT; MALE; MEAN CORPUSCULAR VOLUME; NONHUMAN; PRIORITY JOURNAL;

EID: 0033121167     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v93.7.2404.407k13_2404_2410     Document Type: Article

References (44)

1. Lande WM, Mentzer WC: Haemolytic anaemia associated with increased cation permeability. Clin Haematol 14:89, 1985
2. Lande WM, Thiemann PVW, Mentzer WC Jr: Missing band 7 membrane protein in two patients with high Na, low K erythrocytes. J Clin Invest 70:1273, 1982
3. Eber SW, Lande WM, Iarocci TA, Mentzer WC, Hohn P, Wiley JS, Schroter W: Hereditary stomatocytosis: Consistent association with an integral membrane protein deficiency. Br J Haematol 72:452, 1989
4. -)-cotransport in a case of congenital stomatocytosis. Br J Haematol 71:141, 1989
5. + stomatocytic erythrocytes. Blood 79:1593, 1992
6. Kanzaki A, Yawata Y: Hereditary stomatocytosis: Phenotypical expression of sodium transport and band 7 peptides in 44 cases. Br J Haematol 82:133, 1992
7. Stewart GW, Argent AC, Dash BCJ: Stomatin: A putative cation transport regulator in the red cell membrane. Biochim Biophys Acta 1225:15, 1993
8. Wang D, Mentzer WC, Cameron T, Johnson RM: Purification of band 7.2b, a 31-kDa integral phosphoprotein absent in hereditary stomatocytosis. J Biol Chem 266:17826, 1991
9. Hiebl-Dirschmied CM, Adolf GR, Prohaska R: Isolation and partial characterization of the human erythrocyte band 7 integral membrane protein. Biochim Biophys Acta 1061:195, 1991
10. Salzer U, Ahorn H, Prohaska R: Identification of the phosphorylation site on human erythrocyte band 7 integral membrane protein: Implications for a monotopic protein structure. Biochim Biophys Acta 1151:149, 1993
11. Huang M, Gu G, Ferguson EL, Chalfie M: A stomatin-like protein necessary for mechanosensation in C. elegans. Nature 378:292, 1995
12. Gallagher PG, Forget BG: Structure, organization, and expression of the human band 7.2b gene, a candidate gene for hereditary hydrocytosis. J Biol Chem 270:26358, 1995
13. Gallagher PG, Turetsky T, Mentzer WC: Genomic organization and 5′ flanking DNA sequence of the murine stomatin gene (Epb72). Genomics 34:410, 1996
14. Hiebl-Dirschmied CM, Entler B, Glotzmann C, Maurer-Fogy I, Stratowa C, Prohaska R: Cloning and nucleotide sequence of cDNA encoding human erythrocyte band 7 integral membrane protein. Biochim Biophys Acta 1090:123, 1991
15. Wang D, Teretsky T, Perrine S, Johnson RM, Mentzer WC: Further studies on RBC membrane protein 7.2b deficiency in hereditary stomatocytosis. Blood 80:275a, 1992 (suppl 1)
16. Gallagher PG, Segel G, Marchesi SL, Forget BG: The gene for erythrocyte band 7.2b in hereditary stomatocytosis. Blood 80:276a, 1992 (suppl 1)
17. Gallagher PG, Romana M, Lieman JH, Ward DC: cDNA structure, tissue-specific expression and chromosomal localization of the murine band 7.2b gene. Blood 86:359, 1995
18. Schlegel W, Unfried I, Prohaska R: Cloning and analysis of a cDNA encoding the BALB/c murine erythrocyte band 7 integral membrane protein. Gene 178:115, 1996
19. Paszty C, Mohandas N, Stevens ME, Loring JF, Liebhaber SA, Brion CM, Rubin EM: Lethal a-thalassaemia created by gene targeting in mice and its genetic rescue. Nat Genet 11:33, 1995
20. Chen EY, Liao Y-C, Smith DH, Barrera-Saldana HA, Gelinas RE, Seeburg PH: The human growth hormone locus: Nucleotide sequence, biology and evolution. Genomics 4:479, 1989
21. Nagy A, Rossant J, Nagy R, Abramow-Newerly W, Roder J: Derivation of completely cell culture-derived mice from early-passage embryonic stem cells. Proc Natl Acad Sci USA 90:8424, 1993
22. Sedivy JM, Joyner AL: Gene Targeting. Freeman, New York, NY, 1992
23. Krauss SW, Larabell CA, Lockett S, Gascard P, Penman S, Mohandas N, Chasis JA: Structural protein 4.1 in the nucleus of human cells: Dynamic rearrangements during cell division. J Cell Biol 137:275, 1997
24. Paszty C, Brion CM, Manci E, Witkowska HE, Stevens ME, Mohandas N, Rubin EM: Transgenic knockout mice with exclusively human sickle hemoglobin and sickle cell disease. Science 278:876, 1997
25. Clark MR, Mohandas N, Shohet SB: Osmotic gradient ektacytometry: Comprehensive characterization of red cell volume and surface maintenance. Blood 61:899, 1983
26. Armsby CC, Brugnara C, Alper SL: Cation transport in mouse erythrocytes: Role of K(+)-Cl-cotransport in regulatory volume decrease. Am J Physiol 268:C894, 1995
27. Joiner, CH, Franco RS, Jiang M, France MS, Barker JE, Lux SE: Increased cation permeability in mutant mouse red blood cells with defective membrane skeletons. Blood 86:4307, 1995
28. Kuypers FA, Lewis RA, Ernst JD, Discher D, Lubin BH: Detection of altered membrane phospholipid asymmetry in subpopulations of human red cells using fluorescently labeled annexin V. Blood 87:1179, 1996
29. Kuypers FA: Phospholipid asymmetry in health and disease. Curr Opin Hematol 5:122, 1998
30. Ho MM, Nicolaou A, Argent AC, Stewart GW: Trans-bilayer phospholipid movements in human red blood cells deficient in the 32 kDa band-7.2b membrane protein "stomatin." Biochem Soc Trans 25:492S, 1997
31. Alloisio N, Dalla Venezia N, Rana A, Andrabi K, Texier P, Gilsanz F, Cartron J-P, Delaunay J, Chishti AH: Evidence that red blood cell protein p55 may participate in the skeleton-membrane linkage that involves protein 4.1 and glycophorin C. Blood 82: 1323, 1993
32. Wang K, Richards FM: An approach to nearest neighbor analysis of membrane proteins. J Biol Chem 249:8005, 1974
33. Sinard JH, Stewart GW, Argent AC, Morrow JS: Stomatin binding to adducin: A novel link between transmembrane ion transport and the cytoskeleton. Mol Biol Cell 5:421a, 1994 (suppl)
34. Moore RB, Shriver SK: Protein 7.2b of human erythrocyte membranes binds to calpromotin. Biochem Biophys Res Commun 232:294, 1997
35. Mayer H, Salzer U, Breuss J, Ziegler S, Marchler-Bauer A, Prohaska R: Isolation, molecular characterization, and tissue-specific expression of a novel putative G protein-coupled receptor. Biochim Biophys Acta 1395:301, 1998
36. Snyers L, Thines-Sempoux D, Prohaska R: Colocalization of stomatin (band 7.2b) and actin microfilaments in UAC epithelial cells. Eur J Cell Biol 73:281, 1997
37. Snyers L, Umlauf E, Prohaska R: Oligomeric nature of the integral membrane protein Stomatin. J Biol Chem 273:17221, 1998
38. Peters LL, Shivdasani PA, Liu S-C, Hanspal M, John KM, Gonzalez JM, Brugnara C, Gwynn B, Mohandas N, Alper SL, Orkin SH, Lux SE: Anion exchanger 1 (band 3) is required to prevent erythrocyte membrane surface loss but not to form the membrane skeleton. Cell 86:917, 1996
39. Peters LL, Gwynn B, John KM, Korsgren C, Ciciotte SL, Cohen CM, Lux SE, Brugnara C: Mild spherocytic anemia and altered red blood cell ion transport in mice deficient in protein 4.1. Blood 90:266a, 1997 (suppl 1)
40. Shi Z-T, Walensky LD, Snyder SH, Nelson RJ, Conboy JG, Mohandas N, Rubin E: Protein 4.1-R knockout mice exhibit mechanically unstable erythrocytes and unexpected neurological defects. Blood 90:266a, 1997 (suppl 1)
41. Shohet SB: Reconstitution of spectrin-deficient, spherocytic mouse erythrocyte membranes. J Clin Invest 64:483, 1979
42. Desneves J, Berman A, Dynon K, LaGreca N, Foley M, Tilley L: Human erythrocyte band 7.2b is preferentially labeled by a photoreactive phospholipid. Biochem Biophys Res Commun 224:108, 1996
43. Barnes TM, Jin Y, Horvitz HR, Ruvkun G, Hekimi S: The Caenorhabditis elegans behavioral gene unc-24 encodes a novel bipartite protein similar to both erythrocyte band 7.2 (stomatin) and nonspecific lipid transfer protein. J Neurochem 67:46, 1996
44. Kuypers FA, Yee M, Mentzer WC: Phospholipid composition and organization in protein 7.2b deficient human erythrocytes. Blood 80:273a, 1992 (suppl 1)