Time-dependent changes in the density and hemoglobin F content of biotin-labeled sickle cells

被引:66
作者
Franco, RS
Lohmann, J
Silberstein, EB
Mayfield-Pratt, G
Palascak, M
Nemeth, TA
Joiner, CH
Weiner, M
Rucknagel, DL
机构
[1] Univ Cincinnati, Coll Med, Div Hematol Oncol, Cincinnati, OH 45267 USA
[2] Childrens Hosp Res Fdn, Cincinnati, OH 45229 USA
[3] Cincinnati Comprehens Sickle Cell Ctr, Cincinnati, OH 45229 USA
[4] Cincinnati Vet Adm Med Ctr, Cincinnati, OH 45220 USA
关键词
red blood cell; sickle cell disease; biotin; red cell survival; flow cytometry;
D O I
10.1172/JCI2484
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Sickle 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 (51)Cr label, and used it to study changes that occur in sickle cells as they age, Sickle RBC had 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 similar to 2 wk, whereas F cells survived 6-8 wk.
引用
收藏
页码:2730 / 2740
页数:11
相关论文
共 28 条
[1]   Pulmonary entrapment of sickle cells: The role of regional alveolar hypoxia [J].
Aldrich, TK ;
Dhuper, SK ;
Patwa, NS ;
Makolo, E ;
Suzuka, SM ;
Najeebi, SA ;
Santhanakrishnan, S ;
Nagel, RL ;
Fabry, ME .
JOURNAL OF APPLIED PHYSIOLOGY, 1996, 80 (02) :531-539
[2]   RED-BLOOD-CELL CHANGES DURING THE EVOLUTION OF THE SICKLE-CELL PAINFUL CRISIS [J].
BALLAS, SK ;
SMITH, ED .
BLOOD, 1992, 79 (08) :2154-2163
[3]   IRREVERSIBLY SICKLED ERYTHROCYTES - A CONSEQUENCE OF HETEROGENOUS DISTRIBUTION OF HEMOGLOBIN TYPES IN SICKLE-CELL ANEMIA [J].
BERTLES, JF ;
MILNER, PFA .
JOURNAL OF CLINICAL INVESTIGATION, 1968, 47 (08) :1731-&
[4]  
Campbell T. A., 1997, Blood, V90, p126A
[5]  
CASTRO O, 1976, J LAB CLIN MED, V88, P732
[6]   THE MEASUREMENT OF THE TOTAL VOLUME OF RED-CELLS IN MAN - A NON-RADIOACTIVE APPROACH USING BIOTIN [J].
CAVILL, I ;
TREVETT, D ;
FISHER, J ;
HOY, T .
BRITISH JOURNAL OF HAEMATOLOGY, 1988, 70 (04) :491-493
[7]  
CHRISTIAN JA, 1993, BLOOD, V82, P3469
[8]   DENSITY FRACTIONATION OF ERYTHROCYTES BY PERCOLL HYPAQUE RESULTS IN ONLY A SLIGHT ENRICHMENT FOR AGED CELLS [J].
DALE, GL ;
NORENBERG, SL .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1036 (03) :183-187
[9]  
DALE GL, 1991, ADV EXP MED BIOL, V307, P93
[10]  
DALE GL, 1991, BLOOD, V77, P1096