CD36-positive stress reticulocytosis in sickle cell anemia

Journal of Laboratory and Clinical Medicine

Volumn 127, Issue 4, 1996, Pages 340-347

  Browne, Paul V ^a   Hebbel, Robert P ^a  

^a UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CD36 ANTIGEN;

ARTICLE; BLOOD; CHEMISTRY; COMPARATIVE STUDY; DENSITY GRADIENT CENTRIFUGATION; FLOW CYTOMETRY; HEMATOLOGIC DISEASE; HUMAN; RETICULOCYTE; RETICULOCYTE COUNT; SCANNING ELECTRON MICROSCOPY; SICKLE CELL ANEMIA; SPLENECTOMY; ULTRASTRUCTURE;

ANEMIA, SICKLE CELL; ANTIGENS, CD36; CENTRIFUGATION, DENSITY GRADIENT; FLOW CYTOMETRY; HEMATOLOGIC DISEASES; HUMANS; MICROSCOPY, ELECTRON, SCANNING; RETICULOCYTE COUNT; RETICULOCYTES; SPLENECTOMY;

EID: 0030119698     PISSN: 00222143     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-2143(96)90181-X     Document Type: Article

References (31)

1. Platt OS, Thorington BD, Brambilla DJ, et al. Pain in sickle cell disease. Rates and risk factors. N Engl J Med 1991;325: 11-6.
2. San Biagio PL, Hofrichter J, Mozzarelli A, Henry ER, Eaton WA. Current perspectives on the kinetics of hemoglobin S gelation. Ann NY Acad Sci 1989;565:53-62.
3. Hebbel RP, Mohandas N. Sickle cell adherence. In: Embury SH, Hebbel RP, Mohandas N, Steinberg MH, eds. Sickle cell disease: basic principles and clinical practice. New York: Raven Press, 1994:217-30.
4. Hebbel RP, Boogaerts MAB, Eaton JW, Steinberg MH. Erythrocyte adherence to endothelium in sickle-cell anemia. A possible determinant of disease severity. N Engl J Med 1980;302:992-5.
5. Sugihara K, Sugihara T, Mohandas N, Hebbel RP. Thrombospondin mediates adherence of CD36+ sickle reticulocytes to endothelial cells. Blood 1992;80:2634-42.
6. Brittain HA, Eckman JR, Swerlick RA, Howard RJ, Wick TM. Thrombospondin from activated platelets promotes sickle erythrocyte adherence to human microvascular endothelium under physiologic flow: a potential for platelet activation in sickle cell vaso-occlusion. Blood 1993;81:2137-43.
7. Greenwalt DE, Lipsky RH, Ockenhouse CF, et al. Membrane glycoprotein CD36: a review of its roles in adherence, signal transduction, and transfusion medicine. Blood 1992; 80:1105-15.
8. Okumura N, Tsuji K, Nakahata T. Changes in cell surface antigen expressions during proliferation and differentiation of human erythroid progenitors. Blood 1992;80:642-50.
9. Diggs LW. Siderofibrosis of the spleen in sickle cell anemia. JAMA 1935;104:538-41.
10. Sorette MP, Shiffer K, Clark MR. Improved isolation of normal human reticulocytes via exploitation of chloride-dependent potassium transport. Blood 1992;80:249-54.
11. Bessis M, Breton-Gorius J. Le reticulocyte. Colorations vitales et microscopie electronique. Nouv Rev Fr Hemat 1964; 4:77-94.
12. Mel HC, Prenant M, Mohandas N. Reticulocyte motility and form: studies on maturation and classification. Blood 1977; 49:1001-9.
13. Coulombel L, Tchernia G, Mohandas N. Human reticulocyte maturation and its relevance to erythropoietic stress. J LAB CLIN MED 1979;94:467-74.
14. Noble NA, Xu Q-P, Ward JH. Reticulocytes I. Isolation and in vitro maturation of synchronized populations. Blood 1989; 74:475-81.
15. Joneckis CC, Ackley RL, Orringer EP, Wayner EA, Parise LV. Integrin alpha-4 beta-1 and glycoprotein IV (CD36) are expressed on circulating reticulocytes in sickle cell anemia. Blood 1993;82:3548-55.
16. Perrotta AL, Finch CA. The polychromatophilic erythrocyte. Am J Clin Pathol 1972;57:471-7.
17. Brecher G, Haley JE, Prenant M, Bessis M. Macronormoblasts, macroreticulocytes and macrocytes. Blood Cells 1975; 1:547-56.
18. Noble NA, Xu Q-P, Hoge LL. Reticulocytes II: reexamination of the in vivo survival of stress reticulocytes. Blood 1980;75:1877-82.
19. Patel VP, Ciechanover A, Platt O, Lodish HF. Mammalian reticulocytes lose adhesion to fibronectin during maturation to erythrocytes. Proc Natl Acad Sci 1985;82:440-4.
20. van Schravendijk MR, Handunetti SM, Barnwell JW, Howard RJ. Normal human erythrocytes express CD36, an adhesion molecule of monocytes, platelets, and endothelial cells. Blood 1992;80:2105-14.
21. Asch AS, Tepler J, Silbiger S, Nachman RL. Cellular attachment to thrombospondin. Cooperative interactions between receptor systems. J Biol Chem 1991;266:1740-5.
22. Asch AS, Barnwell J, Silverstein RL, Nachman RL. Isolation of the thrombospondin membrane receptor. J Clin Invest 1987;79:1054-61.
23. Li WX, Howard RJ, Leung LL. Identification of SVTCG in thrombospondin as the conformation-dependent, high affinity binding site for its receptor, CD36. J Biol Chem 1993;268: 16179-84.
24. Asch AS, Liu I, Bricetti FM, et al. Analysis of CD36 binding domains: ligand specificity controlled by dephosphorylation of an ectodomain. Science 1993;262:1436-40.
25. Browne PV, Mosher D, Steinberg MH, Hebbel RP. Disturbance of plasma and platelet thrombospondin levels in sickle cell anemia. Am J Hematol (in press).
26. Hebbel RP. The sickle erythrocyte in double jeopardy: autoxidation and iron decompartmentalization. Semin Hematol 1990;27:51-69.
27. Shinar E, Rachmilewitz EA. Oxidative denaturation of red blood cells in thalassemia. Semin Hematol 1990;27:70-82.
28. Schreck R, Albermann K, Baeuerle PA. Nuclear factor κB: an oxidative stress-responsive transcription factor of eukaryotic cells (a review). Free Radic Res Commun 1992;7:221-37.
29. Armesilla AL, Vega MA. Structural organization of the gene for human CD36 glycoprotein. J Biol Chem 1994;269:18985-91.
30. Advani R, Mentzer W, Andrews D, Schrier S. Oxidation of hemoglobin F is associated with the aging process of neonatal red blood cells. Pediatric Res 1992;32:165-8.
31. Jain SK. The neonatal erythrocyte and its oxidative susceptibility. Semin Hematol 1989;26:286-300.