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476 Part VI: The Erythrocyte Chapter 31: Structure and Composition of the Erythrocyte 477

39. Buchanan GR, Holtkamp CA, Horton JA: Formation and disappearance of pocked ery- 75. Farquhar JW: Human erythrocytes phosphoglycerides. I. Quantification of plasmalo-
throcytes: Studies in human subjects and laboratory animals. Am J Hematol 25:243, gens, fatty acids and fatty aldehydes. Biochim Biophys Acta 60:80, 1962.
1987. 76. Kirk E: The concentration of lecithin, cephalin, ether-insoluble phosphatide, and cere-
40. Kass L: Origin and composition of Cabot rings in pernicious anemia. Am J Clin Pathol brosides in plasma and red blood cells of normal adults. J Biol Chem 123:637, 1938.
64:53, 1975. 77. Phillips GB, Roome NS: Quantitative chromatographic analysis of the phospholipids of
41. Kass L, Gray RH: Ultrastructural visualization of Cabot rings in pernicious anemia. abnormal human red blood cells. Proc Soc Exp Biol Med 109:360, 1962.
Experientia 32:507, 1976. 78. Westerman MP, Zhang Y, McConnell JP, et al: Ascorbate levels in red blood cells and
42. Jensen WN, Moreno GD, Bessis MC: An electron microscopic description of basophilic urine in patients with sickle cell anemia. Am J Hematol 65:174, 2000.
stippling in red cells. Blood 25:933, 1965. 79. Luecke R, Pearson PB: The microbiological determination of free choline in plasma and
43. Heinz R: Uber Blutdegeneration und Regeneration. Beitr Pathol 29:299, 1901. urine. J Biol Chem 153:259, 1944.
44. Chinprasertsuk S, Piankijagum A, Wasi P: In vivo induction of intraerythrocytic inclu- 80. Beerstecher E, Spangler S, Granick S, et al: Blood vitamins, hormones, enzymes. Blood
sion bodies in hemoglobin H disease: An electron microscopic study. Birth Defects Orig coenzymes: Vertebrates, in Blood and Other Body Fluids, edited by PL Altman, DS Ditt-
Artic Ser 23:317, 1987. mer, p 108. Federation of American Societies for Experimental Biology, Washington,
45. Sansone G, Sciarratta GV, Ivaldi G, Chiappara G: Hb H-like inclusions in red cells of DC, 1961.
patients with unstable haemoglobin. Haematologica 72:481, 1987. 81. Kaplan NO, Lipmann F: The assay of distribution of coenzyme A. J Biol Chem 174:37,
46. Wickramasinghe SN, Hughes M, Higgs DR et al: Ultrastructure of red cells containing 1948.
haemoglobin H inclusions induced by redox dyes. Clin Lab Haematol 3:51, 1981. 82. Klein JR, Perlzweig WA, Handler P: Determination of nicotinic acid in blood cells and
47. Bessis MC, Breton-Gorius J: Iron particles in normal erythroblasts and normal and plasma. J Biol Chem 145:27, 1942.
pathological erythrocytes. J Biophys Biochem Cytol 3:503, 1957. 83. Pearson PB: The pantothenic acid content of the blood of mammalia. J Biol Chem
48. Evans J, Gratzer W, Mohandas N, et al: Fluctuations of the red cell membrane: Relation 140:423, 1941.
to mechanical properties and lack of ATP-dependence. Biophys J 94: 4134, 2008. 84. Masse PG, Mahuren JD, Tranchant C, Dosy J: B-6, vitamers and 4-pyridoxic acid in
49. Mohandas N, Gallagher PG: Red cells: Past, present and future. Blood 112:393, 2008. the plasma, erythrocytes, and urine of postmenopausal women. Am J Clin Nutr 80:946,
50. Discher D, Mohandas N, Evans EA: Molecular maps of red cell deformation: Hidden 2004.
elasticity and in situ connectivity. Science 266:1032, 1994. 85. Burch HB, Bessey OA, Lowry OH: Fluorometric measurements of riboflavin and its
51. Liu SC, Derick LH, Palek J: Visualization of the hexagonal lattice in the erythrocyte natural derivatives in small quantities of blood serum and cells. J Biol Chem 175:457,
membrane skeleton. J Cell Biol 104:527, 1987. 1948.
52. Mohandas N, Clark MR, Jacobs MS, Shohet SB: Analysis of factors regulating erythro- 86. Beutler E: Glutathione reductase: Stimulation in normal subjects by riboflavin supple-
cyte deformability. J Clin Invest 66:563, 1980. mentation. Science 165:613, 1969.
53. Mohandas N, Chasis JA, Shohet SB: The influence of membrane skeleton on red cell 87. Burch HB, Bessey OA, Love RH, Lowry OH: The determination of thiamine and thi-
deformability, membrane material properties and shape. Semin Hematol 20:225, amine phosphates in small quantities of blood and blood cells. J Biol Chem 198:477,
1983. 1952.
54. Chasis JA, Mohandas N: Erythrocyte membrane deformability and stability. Two dis- 88. Beutler E: Red Cell Metabolism: A Manual of Biochemical Methods. Grune & Stratton,
tinct membrane properties which are independently regulated by skeletal protein asso- New York, 1984.
ciations. J Cell Biol 103:343, 1986. 89. Bishop C, Rankine D, Talbott JH: The nucleotides in normal human blood. J Biol Chem
55. Mohandas N, Chasis JA: Red cell deformability, membrane material properties and 234:1233, 1959.
shape: Regulation by transmembrane, skeletal and cytosolic proteins and lipids. Semin 90. Mandel P, Chambon P, Karon H, et al: Nucleotides libres des globules rouges et des
Hematol 30:171, 1993. reticulocytes. Folia Haematol Int Mag Klin Morphol Blutforsch 78:525, 1962.
56. Safeukui I, Buffet P, Delpaine G, et al: Quantitative assessment of sensing and seques- 91. Bartlett GR: Human red cell glycolytic intermediates. J Biol Chem 234:449, 1959.
tration of spherocytic erythrocytes by human spleen: Implications for understanding 92. Yoshikawa H, Nakano M, Miyamoto K, Tatibana M: Phosphorus metabolism in human
clinical variability of membrane disorders. Blood 120:424, 2012. erythrocyte. II. Separation of acid-soluble phosphorus compounds incorporating p32
57. Clark MR, Mohandas N, Caggiano V, Shohet SB: Effects of abnormal cation transport by column chromatography with ion exchange resin. J Biochem 47:635, 1960.
on deformability of desiccytes. J Supramol Struct 8:521, 1978. 93. Beutler E, Mathai CK: A comparison of normal red cell ATP levels as measured by the
58. Evans E, Mohandas N, Leung A: Static and dynamic rigidities of normal and sickle firefly system and the hexokinase system. Blood 30:311, 1967.
erythrocytes: Major influence of cell hemoglobin concentration. J Clin Invest 73:477, 94. Minakami S, Suzuki C, Saito T, Yoshikawa H: Studies on erythrocyte glycolysis. I.
1984. Determination of the glycolytic intermediates in human erythrocytes. J Biochem
59. Pantaleo A, Giribaldi G, Mannu F, et al: Naturally occurring anti-band 3 antibodies 58:543, 1965.
and red cell removal under physiological and pathological conditions. Autoimmun Rev 95. Patterson WD, Hardman JG, Sutherland EW: A comparison of cyclic nucleotide levels
7:457, 2008. in plasma and cells of rat and human blood. Endocrinology 95:325, 1974.
60. Arashiki N, Kimata N, Manno S, et al: Membrane peroxidation and methemoglobin 96. Canepa L, Ferraris AM, Miglino M, Gaetani GF: Bound and unbound pyridine dinu-
formation are both necessary for band 3 clustering: Mechanistic insights into erythro- cleotides in normal and glucose-6-phosphate dehydrogenase-deficient erythrocytes.
cyte senescence. Biochemistry 52:5760, 2013. Biochim Biophys Acta 1074:101, 1991.
61. Cooper RA: Loss of membrane components in pathogenesis of antibody-induced 97. Micheli V, Simmonds HA, Bari M, Pompucci G: HPLC determination of oxidized and
spherocytosis. J Clin Invest 51:16, 1972. reduced pyridine coenzymes in human erythrocytes. Clin Chim Acta 220:1, 1993.
62. Lock SP, Smith RS, Hardisty RM: Stomatocytosis: A hereditary red cell anomaly associ- 98. Lagendijk J, Ubbink JB, Vermaak WJH: Quantification of erythrocyte S-adenosyl-l-
ated with haemolytic anaemia. Br J Haematol 7:303, 1961. methionine levels and its application in enzyme studies. J Chromatogr B Biomed Appl
63. Delaunay J, Stewart G, Iolascon A: Hereditary dehydrated and overhydrated stomatoc- 576:95, 1992.
ytosis: Recent advances. Curr Opin Hematol 6:110, 1999. 99. Overgard-Hansen K, Jorgensen S: Determination and concentration of adenine nucle-
64. Delaunay J: The molecular basis of hereditary red cell membrane disorders. Blood Rev otides in human blood. Scand J Clin Lab Invest 12:10, 1960.
21:1, 2007. 100. Mills GC: Uridine diphosphate glucose and uridine diphosphate N-acetylglucosamine
65. De Franceschi L, Bosman GJ, Mohandas N: Abnormal red cell features associated with in erythrocytes. Tex Rep Biol Med 18:446, 1960.
hereditary neurodegenerative disorders: The neuroacanthocytosis syndromes. Curr 101. Liang HR, Takagaki T, Foltz RL, Bennett P: Quantitative determination of endogenous
Opin Hematol 21:201, 2014. sorbitol and fructose in human erythrocytes by atmospheric-pressure chemical ion-
66. Cooper RA, Jandl JH: Bile salts and cholesterol in the pathogenesis of target cells in ization LC tandem mass spectrometry. J Chromatogr B Analyt Technol Biomed Life Sci
obstructive jaundice. J Clin Invest 47:809, 1968. 824:36, 2005.
67. Padilla F, Bromberg PA, Jensen WN: Sickle–unsickle cycle—Cause of cell fragmenta- 102. Lionetti FJ, McLellan WL, Fortier NL, Foster JM: Phosphate esters produced from
tion leading to permanently deformed cells. Blood 41:653, 1973. inosine in human erythrocyte ghosts. Arch Biochem 94:7, 1961.
68. Horiuchi K, Ballas SK, Asakura T: The effect of deoxygenation rate on the formation of 103. Kawaguchi M, Fujii T, Kamiya Y, et al: Effects of fructose ingestion on sorbitol and
irreversibly sickled cells. Blood 71:46, 1988. fructose 3-phosphate contents of erythrocytes from healthy men. Acta Diabetol 33:100,
69. Bertles JF, Milner PF: Irreversibly sickled erythrocytes: A consequence of the hetero- 1996.
geneous distribution of hemoglobin types in sickle-cell anemia. J Clin Invest 47:1731, 104. Petersen A, Szwergold BS, Kappler F, et al: Identification of sorbitol 3-phosphate
1968. and fructose 3-phosphate in normal and diabetic human erythrocytes. J Biol Chem
70. Bull BS, Kuhn IN: Production of schistocytes by fibrin strands (a scanning electron 265:17424, 1990.
microscope study). Blood 35:104, 1970. 105. Colomer D, Pujades A, Carballo E, Vives Corrons JL: Erythrocyte fructose 2,6-bisphos-
71. Ponder E: Hemolysis and Related Phenomena. Grune & Stratton, New York, 1948. phate content in congenital hemolytic anemias. Hemoglobin 15:517, 1991.
72. Behrendt H: Chemistry of Erythrocytes. Charles C Thomas, Springfield, IL, 1957. 106. Deichmann WB, Dierker M: The spectrophotometric estimation of hexuronates
73. Tyan YC, Jong SB, Liao JD, et al: Proteomic profiling of erythrocyte proteins by prote- (expressed as glucuronic acid) in plasma or serum. J Biol Chem 163:753, 1946.
olytic digestion chip and identification using two-dimensional electrospray ionization 107 Jung CY: Carrier-mediated glucose transport across human red cell membranes, in The
tandem mass spectrometry. J Proteome Res 4:748, 2005. Red Blood Cell, edited by DM Surgenor, p 705. Academic Press, New York, 1975.
74. Pasini EM, Kirkegaard M, Mortensen P, et al: In-depth analysis of the membrane and 108. Lacko L, Wittke B, Geck P: The temperature dependence of the exchange transport of
cytosolic proteome of red blood cells. Blood 108:791, 2006. glucose in human erythrocytes. J Cell Physiol 82:213, 1973.

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