TY - JOUR
T1 - Characterization of acatalasemic erythrocytes treated with low and high dose hydrogen peroxide
T2 - Hemolysis and aggregation
AU - Masuoka, Noriyoshi
AU - Sugiyama, Hitoshi
AU - Ishibashi, Naoki
AU - Wang, Da Hong
AU - Masuoka, Takayoshi
AU - Kodama, Hiroyuki
AU - Nakano, Taku
PY - 2006/8/4
Y1 - 2006/8/4
N2 - The effects of hydrogen peroxide on normal and acatalasemic erythrocytes were examined. Severe hemolysis of acatalasemic erythrocytes and a small tyrosine radical signal (g = 2.005) associated with the formation of ferryl hemoglobin were observed upon the addition of less than 0.25 mM hydrogen peroxide. However, when the concentration of hydrogen peroxide was increased to 0.5 mM, acatalasemic erythrocytes became insoluble in water and increased the tyrosine radical signal. Polymerization of hemoglobin and aggregation of the erythrocytes were observed. On the other hand, normal erythrocytes exhibited only mild hemolysis by the addition of hydrogen peroxide under similar conditions. From these results, the scavenging of hydrogen peroxide by hemoglobin generates the ferryl hemoglobin species (H-Hb-Fe(IV)=O) plus protein-based radicals ( .Hb-Fe(IV)=O). These species induce hemolysis of erythrocytes, polymerization of hemoglobin, and aggregation of the acatalasemic erythrocytes. A mechanism for the onset of Takarara disease is proposed.
AB - The effects of hydrogen peroxide on normal and acatalasemic erythrocytes were examined. Severe hemolysis of acatalasemic erythrocytes and a small tyrosine radical signal (g = 2.005) associated with the formation of ferryl hemoglobin were observed upon the addition of less than 0.25 mM hydrogen peroxide. However, when the concentration of hydrogen peroxide was increased to 0.5 mM, acatalasemic erythrocytes became insoluble in water and increased the tyrosine radical signal. Polymerization of hemoglobin and aggregation of the erythrocytes were observed. On the other hand, normal erythrocytes exhibited only mild hemolysis by the addition of hydrogen peroxide under similar conditions. From these results, the scavenging of hydrogen peroxide by hemoglobin generates the ferryl hemoglobin species (H-Hb-Fe(IV)=O) plus protein-based radicals ( .Hb-Fe(IV)=O). These species induce hemolysis of erythrocytes, polymerization of hemoglobin, and aggregation of the acatalasemic erythrocytes. A mechanism for the onset of Takarara disease is proposed.
UR - http://www.scopus.com/inward/record.url?scp=33746835312&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33746835312&partnerID=8YFLogxK
U2 - 10.1074/jbc.M513818200
DO - 10.1074/jbc.M513818200
M3 - Article
C2 - 16751193
AN - SCOPUS:33746835312
SN - 0021-9258
VL - 281
SP - 21728
EP - 21734
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 31
ER -