PARTIALLY OXYGENATED SICKLED CELLS - SICKLE-SHAPED RED-CELLS FOUND IN CIRCULATING BLOOD OF PATIENTS WITH SICKLE-CELL DISEASE

被引:24
作者
ASAKURA, T
MATTIELLO, JA
OBATA, K
ASAKURA, K
REILLY, MP
TOMASSINI, N
SCHWARTZ, E
OHENEFREMPONG, K
机构
[1] UNIV PENN,SCH MED,DEPT PEDIAT,PHILADELPHIA,PA 19104
[2] UNIV PENN,SCH MED,DEPT BIOCHEM & BIOPHYS,PHILADELPHIA,PA 19104
[3] UNIV PENN,SCH MED,DEPT HUMAN GENET,PHILADELPHIA,PA 19104
关键词
D O I
10.1073/pnas.91.26.12589
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A previously uncharacterized type of sickled cell was found in venous blood of patients with sickle cell disease when blood was collected without exposure to air and fixed immediately with 1% glutaraldehyde solution equilibrated with 5% oxygen. These cells were either elongated, resembling irreversibly sickled cells (ISCs), or nonelongated, with a raisin-like shape. Both types assumed a normal discoidal shape upon full oxygenation. Since these cells exist only under partially oxygenated conditions, they are described as partially oxygenated sickled cells (POSCs). POSCs are morphologically distinct from partially deoxygenated sickled cells formed during deoxygenation by having rounded edges, while the latter have sharp edges. Transmission electron microscopy of POSCs revealed various amounts of misaligned Hb S polymers. Investigations in vitro demonstrated the formation of POSC-like cells by partial oxygenation of deoxygenated cells. Since POSCs contain intracellular fibers and sickle readily upon deoxygenation, they may have clinical and pathological significance.
引用
收藏
页码:12589 / 12593
页数:5
相关论文
共 27 条
[1]  
ALLISON AC, 1956, CLIN SCI, V15, P497
[2]  
ASAKURA T, 1984, J LAB CLIN MED, V104, P987
[3]   AUTOMATED-METHOD FOR DETERMINATION OF OXYGEN EQUILIBRIUM CURVES OF RED-CELL SUSPENSIONS UNDER CONTROLLED BUFFER CONDITIONS AND ITS CLINICAL APPLICATIONS [J].
ASAKURA, T .
CRITICAL CARE MEDICINE, 1979, 7 (09) :391-395
[4]  
ASAKURA T, 1992, BLOOD, V80, P9
[5]   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-&
[6]  
BRIEHL RW, 1994, BLOOD, V83, P573
[7]  
Eaton W A, 1990, Adv Protein Chem, V40, P63, DOI 10.1016/S0065-3233(08)60287-9
[8]  
HAHN EV, 1927, ARCH INTERN MED, V239, P233
[9]  
HAHN JA, 1956, BRIT J HAEMATOL, V34, P559
[10]   STUDIES ON THE DESTRUCTION OF RED BLOOD CELLS .10. THE BIOPHYSICS AND BIOLOGY OF SICKLE-CELL DISEASE [J].
HARRIS, JW ;
BREWSTER, HH ;
HAM, TH ;
CASTLE, WB .
ARCHIVES OF INTERNAL MEDICINE, 1956, 97 (02) :145-168