Literature DB >> 7074218

Spectrin tetramer-dimer equilibrium in hereditary elliptocytosis.

T Coetzer, S Zail.   

Abstract

The proportion of spectrin tetramers and dimers in 4 degrees C low ionic strength extracts of red cell membranes of 9 subjects with 4 different variants of hereditary elliptocytosis (HE) and 2 subjects with hereditary spherocytosis (HS) was determined by nondenaturing gel electrophoresis. Such extracts reflect the native oligomeric state of spectrin in the red cell membrane. In two hemolytic HE variants (an unclassified adult with increased thermal sensitivity of red cells and an infant also showing increased thermal sensitivity of red cells), the proportion of dimers was increased, whereas the remaining subjects had values within the control range. Conversion of spectrin tetramers to dimers under isotonic conditions at 37 degrees C, or spectrin dimers to tetramers at 30 degrees C, resulted in a high proportion of dimers in the above two HE variants, as well as in a third variant with probable mild HE and sporadic hemolysis. The mother of the infant with elliptocytosis and increased thermal sensitivity of red cells, although hematologically normal, had an increased proportion of dimers in 4 degrees C low ionic strength extracts of her red cell membranes. These findings reflect an underlying primary or secondary abnormality of spectrin in these subjects that affects the association state of spectrin in the red cell membrane. Their exact relationship to the pathogenesis of the elliptical shape of the red cell, or to the presence of hemolysis, is at present unclear.

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Year:  1982        PMID: 7074218

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  11 in total

1.  Immunocytochemical study of membrane skeletons in abnormally shaped erythrocytes as revealed by a quick-freezing and deep-etching method.

Authors:  S Ohno; N Terada; Y Fujii; H Ueda; H Kuramoto; N Kamisawa
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1993

2.  Abnormalities in the erythrocyte membrane in acute lymphoid leukaemia.

Authors:  M Kundu; J Basu; P Chakrabarti; M M Rakshit
Journal:  Biochem J       Date:  1989-03-15       Impact factor: 3.857

3.  Interactions of spectrin in hereditary elliptocytes containing truncated spectrin beta-chains.

Authors:  S W Eber; S A Morris; W Schröter; W B Gratzer
Journal:  J Clin Invest       Date:  1988-02       Impact factor: 14.808

4.  Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis.

Authors:  P A Lane; R L Shew; T A Iarocci; N Mohandas; T Hays; W C Mentzer
Journal:  J Clin Invest       Date:  1987-03       Impact factor: 14.808

5.  Four different mutations in codon 28 of alpha spectrin are associated with structurally and functionally abnormal spectrin alpha I/74 in hereditary elliptocytosis.

Authors:  T L Coetzer; K Sahr; J Prchal; H Blacklock; L Peterson; R Koler; J Doyle; J Manaster; J Palek
Journal:  J Clin Invest       Date:  1991-09       Impact factor: 14.808

6.  Defective binding of spectrin to ankyrin in a kindred with recessively inherited hereditary elliptocytosis.

Authors:  S S Zail; T L Coetzer
Journal:  J Clin Invest       Date:  1984-09       Impact factor: 14.808

7.  Structural and functional effects of hereditary hemolytic anemia-associated point mutations in the alpha spectrin tetramer site.

Authors:  Massimiliano Gaetani; Sara Mootien; Sandra Harper; Patrick G Gallagher; David W Speicher
Journal:  Blood       Date:  2008-01-24       Impact factor: 22.113

8.  Comparison between erythrocyte hemoglobin and spectrin glycosylation and role of oxidative stress in type-2 diabetes mellitus.

Authors:  Y S Mahindrakar; A N Suryakar; R D Ankush; R V Katkam; K M Kumbhar
Journal:  Indian J Clin Biochem       Date:  2007-03

9.  Hereditary pyropoikilocytosis and elliptocytosis in a Caucasian family. Transmission of the same molecular defect in spectrin through three generations with different clinical expression.

Authors:  M C Lecomte; D Dhermy; M Garbarz; C Feo; H Gautero; O Bournier; C Picat; I Chaveroche; C Galand; P Boivin
Journal:  Hum Genet       Date:  1987-12       Impact factor: 4.132

10.  Pathologic and nonpathologic variants of the spectrin molecule in two black families with hereditary elliptocytosis.

Authors:  M C Lecomte; D Dhermy; M Garbarz; C Feo; H Gautero; O Bournier; C Picat; I Chaveroche; A Ester; C Galand
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

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