Literature DB >> 5658583

Hemoglobin CC disease: rheological properties or erythrocytes and abnormalities in cell water.

J R Murphy.   

Abstract

Suspensions of erythrocytes from patients with hemoglobin (Hb) CC disease showed an increased viscosity and decreased filterability suggesting a less deformable cell. Hemolysates prepared from Hb CC erythrocytes had an increased viscosity compared with hemolysates of normal cells, suggesting that the increased viscosity of Hb CC cells in serum was the result of an increased internal viscosity of the cell. These abnormal rheological properties of Hb CC erythrocytes were associated with a decreased content of cations and an abnormality of cell water. The fraction of the cell volume, which is water in Hb CC cells, was 95.5% of normal. The amount of cell water in Hb CC cells available for osmotic equilibrium, termed solvent water, was only 67% of that in normal cells. The smaller amount of solvent water in Hb CC cells indicates a greater amount of water bound to protein. Altered rheological properties of erythrocytes with Hb AA, CC, and SC also were observed during pregnancy. Suspensions of erythrocytes in serum or plasma from pregnant patients resulted in an increased viscosity compared with suspension in serum or plasma from nonpregnant individuals. An increased viscosity during pregnancy is consistent with the increased severity of the hemolytic anemia in patients with these hemoglobinopathies during pregnancy. The studies reported here suggest that in Hb CC disease the mechanism of erythrocyte destruction, splenic sequestration, results from the increased viscosity, and less deformability of the erythrocyte with on increased internal viscosity.

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Year:  1968        PMID: 5658583      PMCID: PMC297308          DOI: 10.1172/JCI105842

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  31 in total

1.  A MOLECULAR MECHANISM OF SICKLED ERYTHROCYTE FORMATION.

Authors:  M MURAYAMA
Journal:  Nature       Date:  1964-04-18       Impact factor: 49.962

2.  INFLUENCE OF FIBRINOGEN ON FLOW PROPERTIES OF ERYTHROCYTE SUSPENSIONS.

Authors:  R E WELLS; T H GAWRONSKI; P J COX; R D PERERA
Journal:  Am J Physiol       Date:  1964-11

3.  Clinical manifestations of hemoglobin C disorders.

Authors:  E W SMITH; J R KREVANS
Journal:  Bull Johns Hopkins Hosp       Date:  1959-01

4.  An improved procedure for starch-gel electrophoresis: further variations in the serum proteins of normal individuals.

Authors:  O SMITHIES
Journal:  Biochem J       Date:  1959-03       Impact factor: 3.857

5.  In vitro crystallization of hemoglobin occuring in citrated blood from patients with hemoglobin C.

Authors:  A P KRAUS; L W DIGGS
Journal:  J Lab Clin Med       Date:  1956-05

6.  Titratable sulfhydryl groups of hemoglobin C and fetal hemoglobin at 0 degrees and 38 degrees.

Authors:  M MURAYAMA
Journal:  J Biol Chem       Date:  1958-01       Impact factor: 5.157

7.  Studies on abnormal hemoglobins. IX. Pure (homozygous) hemoglobin C disease.

Authors:  K SINGER; A Z CHAPMAN; S R GOLDBERG; H M RUBINSTEIN; S A ROSENBLUM
Journal:  Blood       Date:  1954-11       Impact factor: 22.113

8.  Intraerythrocytic crystals in a white patient with hemoglobin C in the absence of other types of hemoglobin.

Authors:  L W DIGGS; A P KRAUS; D B MORRISON; R P RUDNICKI
Journal:  Blood       Date:  1954-12       Impact factor: 22.113

9.  The biophysics of the variants of sickle-cell disease.

Authors:  R C GRIGGS; J W HARRIS
Journal:  AMA Arch Intern Med       Date:  1956-03

10.  Pathogenesis of hemolytic anemia in homozygous hemoglobin C disease.

Authors:  S Charache; C L Conley; D F Waugh; R J Ugoretz; J R Spurrell
Journal:  J Clin Invest       Date:  1967-11       Impact factor: 14.808

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  5 in total

1.  Analysis of factors regulating erythrocyte deformability.

Authors:  N Mohandas; M R Clark; M S Jacobs; S B Shohet
Journal:  J Clin Invest       Date:  1980-09       Impact factor: 14.808

2.  Rate of activation and deactivation of K:Cl cotransport by changes in cell volume in hemoglobin SS, CC and AA red cells.

Authors:  M Canessa; J R Romero; C Lawrence; R L Nagel; M E Fabry
Journal:  J Membr Biol       Date:  1994-12       Impact factor: 1.843

3.  Regulation of cation content and cell volume in hemoglobin erythrocytes from patients with homozygous hemoglobin C disease.

Authors:  C Brugnara; A S Kopin; H F Bunn; D C Tosteson
Journal:  J Clin Invest       Date:  1985-05       Impact factor: 14.808

4.  Abnormal rheology of oxygenated blood in sickle cell anemia.

Authors:  S Chien; S Usami; J F Bertles
Journal:  J Clin Invest       Date:  1970-04       Impact factor: 14.808

5.  Some aspects of the pathophysiology of homozygous Hb CC erythrocytes.

Authors:  M E Fabry; D K Kaul; C Raventos; S Baez; R Rieder; R L Nagel
Journal:  J Clin Invest       Date:  1981-05       Impact factor: 14.808

  5 in total

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