Nonrandom Association of Free Iron With Membranes of Sickle and ,8-Thalassemic Erythrocytes

نویسندگان

  • Tanya Repka
  • Oded Shalev
  • Ratnammal Reddy
  • Jie Yuan
  • Ayala Abrahamov
  • Eliezer A. Rachmilewitz
چکیده

To further define the nature of abnormal iron deposits on the membranes of pathologic red blood cells, we have used sickle cell anemia (HbSS), HbSC, and @-thalassemic erythrocytes (RBCs) to prepare inside-out membranes (IOM) and insoluble membrane aggregates (AGGs) containing coclustered hemichrome and band 3. Study of IOM from HbSC and thalassemic patients showed that amounts of heme iron and, especially, free iron were much higher in patients who had undergone surgical splenectomy. The membrane AGGs from HbSS and @-thalassemic RBCs contained much more globin than heme, with this discrepancy being variable from patient to patient. Although these AGGs were enriched (compared with the ghosts from

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تاریخ انتشار 2003