Literature DB >> 14367773

The specific heat and the heat of compression of human red cells, sickled red cells, and paracrystalline rat red cells.

E PONDER.   

Abstract

The investigation of two thermal properties of red cells throws some light on whether sickling is a process involving the crystallization of a relatively insoluble hemoglobin. These properties are the specific heat and the heat of compression, both of which would be expected to become numerically less if the hemoglobin of the red cell were to crystallize. In the case of paracrystalline rat red cells, which give spacings at 45 A and 58 A by x-ray diffraction, the specific heat is reduced to 85 per cent of that of the normal red cells, and the heat of compression is only about 75 per cent of that found for the normal red cell. In the case of the red cell sickled by a reduction of the O(2) tension, the specific heat and the heat of compression are substantially the same as found for the normal red cell. This is an argument against sickling being the result of a crystallization process, and supports the observation that sickled cells do not give x-ray spacings. The result is compatible, on the other hand, with sickling being the result of the formation of an oriented and birefringent gel.

Entities:  

Keywords:  ERYTHROCYTES

Mesh:

Substances:

Year:  1955        PMID: 14367773      PMCID: PMC2147504          DOI: 10.1085/jgp.38.5.575

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  3 in total

1.  Studies on abnormal hemoglobins. VIII. The gelling phenomenon of sickle cell hemoglobin: its biologic and diagnostic significance.

Authors:  K SINGER; L SINGER
Journal:  Blood       Date:  1953-11       Impact factor: 22.113

2.  Studies on the destruction of red blood cells. VIII. Molecular orientation in sickle cell hemoglobin solutions.

Authors:  J W HARRIS
Journal:  Proc Soc Exp Biol Med       Date:  1950-10

3.  Diffractometric measurements of the tonicity volume relations of human red cells in hypotonic systems.

Authors:  E PONDER
Journal:  J Gen Physiol       Date:  1951-05       Impact factor: 4.086

  3 in total
  3 in total

1.  Studies of sickle cell anemia. I. The transport of phosphorus across the red cell envelope as measured with radiophosphorus (P32).

Authors:  G P LABAT; T G SHELTON; C STANLEY; H BRANSON
Journal:  J Natl Med Assoc       Date:  1958-01       Impact factor: 1.798

2.  A comparison of the electrophoretic characteristics of the human normal and sickle erythrocyte.

Authors:  G V Seaman; B A Pethica
Journal:  Biochem J       Date:  1964-03       Impact factor: 3.857

3.  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

  3 in total

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