Red blood cell membrane disorders

William T. Tse*, Samuel E. Lux

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

220 Scopus citations

Abstract

The recent discovery of the specific molecular defects in many patients with hereditary spherocytosis and hereditary elliptocytosis/pyropoikilocytosis partially clarifies the molecular pathology of these diseases. HE and HPP are caused by defects in the horizontal interactions that hold the membrane skeleton together, particularly the critical spectrin self-association reaction. Single gene defects cause red cells to elongate as they circulate, by a unknown mechanism, and are clinically harmless. The combination of two defective genes or one severe α spectrin defect and a thalassaemia-like defect in the opposite allele (α(LELY)) results in fragile cells that fragment into bizarre shapes in the circulation, with haemolysis and sometimes life-threatening anaemia. A few of the α spectrin defects are common, suggesting they provide an advantage against malaria or some other threat. HS, in contrast, is nearly always caused by family-specific private mutations. These involve the five proteins that link the membrane skeleton to the overlying lipid bilayer: α and β spectrin, ankyrin, band 3 and protein 4.2. Somehow, perhaps through loss of the anchorage band 3 provides its lipid neighbours (Peters et al, 1996), microvesiculation of the membrane surface ensues, leading to spherocytosis, splenic sequestration and haemolysis. Future research will need to focus on how each type of defect causes its associated disease, how the spleen aggrevates membrane skeleton defects (a process termed 'conditioning'), how defective red cells are recognized and removed in the spleen, and why patients with similar or even identical defects can have different clinical severity. Emphasis also needs to be given to improving diagnostic tests, particularly for HS, and exploring new options for therapy, like partial splenectomy, which can ameliorate symptoms while better protecting patients from bacterial sepsis and red cell parasites, and perhaps from atherosclerosis (Robinette and Fraumeni, 1977) and venous thrombosis (Stewart et al, 1996).

Original languageEnglish (US)
Pages (from-to)2-13
Number of pages12
JournalBritish Journal of Haematology
Volume104
Issue number1
DOIs
StatePublished - 1999

Keywords

  • Ankyrin
  • Elliptocytosis
  • Pyropoikilocytosis
  • Spectrin
  • Spherocytosis

ASJC Scopus subject areas

  • Hematology

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