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R S Franco, J Lohmann, E B Silberstein, G Mayfield-Pratt, M Palascak, T A Nemeth, C H Joiner, M Weiner, D L Rucknagel
J Clin Invest. 1998;
101(12):2730
doi:10.1172/JCI2484
Abstract |
Full text
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S
ickle red blood cells (RBC) are subject to a number of important cellular changes and selection pressures. In this study, we validated a biotin RBC label by comparison to the standard 51Cr label, and used it to study changes that occur in sickle cells as they age. Sickle RBC had a much shorter lifespan than normal RBC, but the two labels gave equivalent results for each cell type. A variable number of sickle, but not normal, RBC disappeared from the circulation during the first few hours after reinfusion. The number of biotinylated sickle reticulocytes was decreased by 50% after 24 h and 75% after 48 h, with a gradual decrease in the amount of reticulum per cell. The labeled sickle cells exhibited major density increases during the first 4-6 d after reinfusion, with smaller changes thereafter. A small population of very light, labeled sickle RBC was essentially constant in number after the first few days. Fetal hemoglobin (HbF) content was determined in isolated biotinylated sickle RBC after reinfusion, allowing an estimate of lifespan for RBC containing HbF (F cells) and non-F cells. The lifespan of sickle biotinylated RBC lacking HbF was estimated to be approximately 2 wk, whereas F cells survived 6-8 wk.
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(20)
| Title and authors |
Publication |
Year |
Reconstructing sickle cell disease: A data-based analysis of the “hyperhemolysis paradigm” for pulmonary hypertension from the perspective of evidence-based medicine
Robert P. Hebbel
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Am. J. Hematol.
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2011 |
Expression patterns of fetal hemoglobin in sickle cell erythrocytes are both patient- and treatment-specific during childhood
Emily Riehm Meier, Colleen Byrnes, Maxine Weissman, Pierre Noel, Naomi L.C. Luban, Jeffery L. Miller
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Pediatr. Blood Cancer
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2011 |
Accelerated removal of antibody-coated red blood cells from the circulation is accurately tracked by a biotin label : RBC SURVIVAL BY BIOTIN
Donald M. Mock, Gary L. Lankford, Nell I. Matthews, Leon F. Burmeister, Daniel Kahn, John A. Widness, Ronald G. Strauss
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Transfusion
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2011 |
The measurement and importance of red cell survival
Robert S. Franco
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Am. J. Hematol.
|
2009 |
A novel human gamma-globin gene vector for genetic correction of sickle cell anemia in a humanized sickle mouse model: critical determinants for successful correction.
Ajay Perumbeti, Tomoyasu Higashimoto, Fabrizia Urbinati, Robert Franco, Herbert J Meiselman, David Witte, Punam Malik
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Blood
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2009 |
Red blood cell volume can be independently determined in vitro using sheep and human red blood cells labeled at different densities of biotin.
Donald M Mock, Nell I Matthews, Ronald G Strauss, Leon F Burmeister, Robert Schmidt, John A Widness
|
Transfusion
|
2009 |
Red cell life span heterogeneity in hematologically normal people is sufficient to alter HbA1c
R. M. Cohen, R. S. Franco, P. K. Khera, E. P. Smith, C. J. Lindsell, P. J. Ciraolo, M. B. Palascak, C. H. Joiner
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Blood
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2008 |
Sickle cell disease vasculopathy: A state of nitric oxide resistance
Katherine C. Wood, Lewis L. Hsu, Mark T. Gladwin
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Free Radical Biology and Medicine
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2008 |
A method for the continuous calculation of the age of labeled red blood cells
Christopher J. Lindsell, Robert S. Franco, Eric P. Smith, Clinton H. Joiner, Robert M. Cohen
|
Am. J. Hematol.
|
2008 |
Effects of age-dependent membrane transport changes on the homeostasis of senescent human red blood cells
V. L. Lew, N. Daw, Z. Etzion, T. Tiffert, A. Muoma, L. Vanagas, R. M. Bookchin
|
Blood
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2007 |
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