Literature DB >> 7265274

The distribution of copper in sickling erythrocytes as determined by an IBM cell separator.

K Schaeffer, J Aikens, M Williamson, E J Olson.   

Abstract

Elevated levels of copper have been found in sickling erythrocytes. Since this copper may inhibit sickling or induce hemolysis the authors decided to investigate the distribution of copper in sickling erythrocytes to gain some insight into its origin. When samples of sickling erythrocytes were fractionated by density gradient centrifugation with an IBM cell separator and the fractions analyzed for copper, it was found that the copper to hemoglobin ratio of the different fractions varied several fold. This finding indicated that the copper in sickling erythrocytes did not equilibrate with the copper in serum or other cells and that the copper was present in the cells when they were released into the blood stream. When erythrocytes were obtained from a sickle cell patient four days post-crises, a large amount of residual copper could be observed in the first (youngest) fraction. It was suspected that this copper was in mitochondrial residues. It was also observed that copper levels tended to be higher in control and sicklings erythrocytes during the winter months. The predominance of the first fraction in samples of sickling erythrocytes taken during the winter months suggests that the turnover of sickling erythrocytes is accelerated at this time.

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Year:  1981        PMID: 7265274      PMCID: PMC2553028     

Source DB:  PubMed          Journal:  J Natl Med Assoc        ISSN: 0027-9684            Impact factor:   1.798


  9 in total

1.  ULTRACENTRIFUGAL FRACTIONATION OF HUMAN ERYTHROCYTES WITH RESPECT TO CELL AGE.

Authors:  L GARBY; M HJELM
Journal:  Blut       Date:  1963-08

2.  Copper-induced generation of superoxide in human red cell membrane.

Authors:  K S Kumar; C Rowse; P Hochstein
Journal:  Biochem Biophys Res Commun       Date:  1978-07-28       Impact factor: 3.575

3.  A comprehensive screening program for hemoglobinopathies.

Authors:  M G Barnes; L Komarmy; A H Novack
Journal:  JAMA       Date:  1972-02       Impact factor: 56.272

4.  Occurrence of copper in sickling erythrocytes.

Authors:  K Schaeffer; J A Lofton; S C Powell; H H Osborne; L H Foster
Journal:  Proc Soc Exp Biol Med       Date:  1968-07

5.  Fractionation studies of copper in erythrocytes from normal, sickle cell anemia, and hemoglobin C disease.

Authors:  K Schaeffer; J E Young; G W Buckaloo; S M Howell
Journal:  Proc Soc Exp Biol Med       Date:  1970-05

6.  The occurrence of lysosome-like structures in sickling erythrocytes.

Authors:  K Schaeffer; B R Brinkley; J E Young; S S Oliver; J P Chang; W M Guillen
Journal:  Lab Invest       Date:  1970-09       Impact factor: 5.662

7.  Hemolytic anemia in Wilson's disease.

Authors:  A Deiss; G R Lee; G E Cartwright
Journal:  Ann Intern Med       Date:  1970-09       Impact factor: 25.391

8.  Copper-induced acute hemolytic anemia. A new complication of hemodialysis.

Authors:  A D Manzler; A W Schreiner
Journal:  Ann Intern Med       Date:  1970-09       Impact factor: 25.391

9.  Irreversibly sickled cells and red cell survival in sickle cell anemia: a study with both DF32P and 51CR.

Authors:  P R McCurdy; A S Sherman
Journal:  Am J Med       Date:  1978-02       Impact factor: 4.965

  9 in total
  1 in total

1.  The Role of Nutrition in Sickle Cell Disease.

Authors:  H I Hyacinth; B E Gee; J M Hibbert
Journal:  Nutr Metab Insights       Date:  2010-01-01
  1 in total

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