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A basis of the acanthocytosis in inherited and acquired disorders
1Department of Oncology, McGill University, 546 Pine Avenue West, Montreal, Que., Canada H2W 1S6. pierre.wong@mcgill.ca
Insights
Acanthocytosis, a red blood cell shape change, is linked to Band 3 protein alterations. This study proposes a mechanism involving Band 3 conformation changes to explain acanthocytosis in various inherited and acquired disorders.
Area of Science:
- Hematology
- Cell Biology
- Biochemistry
Background:
- Acanthocytosis describes erythrocyte transformation into cells with irregular projections.
- It is associated with diverse inherited and acquired conditions.
- Previous work suggested a link between chorea-acanthocytosis and altered Band 3 protein.
Purpose of the Study:
- To propose a mechanism for erythrocyte shape control involving Band 3 protein conformations.
- To explain the occurrence of acanthocytosis in various disorders based on this mechanism.
- To investigate the role of Band 3 conformation and membrane skeleton in erythrocyte shape determination.
Main Methods:
- Proposed a model of erythrocyte shape control based on Band 3 outward-facing (Band 3(o)) and inward-facing (Band 3(i)) conformations.
- Related the Band 3 conformation ratio to the Donnan equilibrium of anions and protons.
- Analyzed evidence linking acanthocytosis to alterations in membrane skeleton and Band 3 properties across different conditions.
Main Results:
- The proposed mechanism explains acanthocytosis in pyruvate kinase deficiency, pyrimidine 5'-nucleotidase deficiency, dehydrated hereditary stomatocytosis, In(Lu) phenotype, chorea-acanthocytosis, and McLeod phenotype via decreased Donnan ratio.
- Alterations in membrane skeleton conformation are consistent with the proposed mechanism in chorea-acanthocytosis, McLeod phenotype, and Fanconi's anemia.
- Acanthocytosis in Band 3 HT variant, chorea-acanthocytosis, In(Lu) phenotype, alcoholic cirrhosis, and abetalipoproteinemia supports the role of Band 3 conformation changes.
Conclusions:
- Erythrocyte shape is significantly determined by Band 3 conformation and membrane skeleton status.
- The proposed mechanism provides a unifying explanation for acanthocytosis in numerous disorders.
- Lipid bilayer changes play a secondary role, with Band 3 conformation being the primary determinant of erythrocyte shape.
Abstract:
Acanthocytosis refers to the transformation of the normal biconcave disc erythrocyte into one with a few irregularly shaped external projections distributed unevenly at its membrane surface. It is associated with a variety of inherited and acquired disorders. A relationship between the acanthocytosis in chorea-acanthocytosis and an alteration of Band 3, the anion exchange protein, has been previously suggested. We have previously proposed a mechanism of erythrocyte shape control in which decrease and increase of the ratio of the outward-facing (Band 3(o)) and inward-facing (Band 3(i)) conformations of Band 3 contracts and relaxes the membrane skeleton, thus promoting echinocytosis and stomatocytosis, respectively. The equilibrium Band 3(o)/Band 3(i) ratio is determined by the Donnan equilibrium ratio of anions and protons, increasing with the increase of the Donnan ratio. Based on the evidence suggesting that the acanthocyte and echinocyte are interrelated, the mechanism could explain by a decrease of the Donnan ratio the occurrence of acanthocytes in pyruvate kinase and pyrimidine 5'-nucleotidase deficiencies, dehydrated hereditary stomatocytocytosis, In(Lu) phenotype, chorea-acanthocytosis, and McLeod phenotype. Consistent with the proposed mechanism indicating that the membrane skeleton is an important determinant of the erythrocyte shape, is the alteration of its conformation in chorea-acanthocytosis, McLeod phenotype and Fanconi's anemia. In agreement with the proposed mechanism indicating that Band 3 conformation controls the erythrocyte shape are the occurrence of an acanthocytosis in individuals expressing the rare Band 3 HT variant and of alterations of Band 3 properties in chorea-acanthocytosis and In(Lu) phenotype. The observations that the lipid composition or organization are normal in chorea-acanthocytosis and McLeod phenotype are supportive of the proposed mechanism since it postulates that the lipid bilayer has a secondary role in determining the erythrocyte shape. The acanthocytoses in alcoholic cirrhosis and abetalipoproteinemia are accompanied by significant increases of the cholesterol level and of the ratio of sphingomyelin and glycerophospholipids, respectively. However, they could occur by a change of the Band 3 conformation since cholesterol binds specifically to Band 3 and inhibits its anion transport activity, and that sphingomyelin potentiates this inhibition. Thus, the acanthocytosis could involve an alteration of the Band 3 conformation.
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