Accumulation of oxidized peroxiredoxin 2 in red blood cells and its prevention

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pp. 1909-1918 ◽  
Author(s):  
Simone B. Bayer ◽  
Mark B. Hampton ◽  
Christine C. Winterbourn
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pp. 2967-2978 ◽  
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Joo-Yeun Oh ◽  
Ryan Stapley ◽  
Victoria Harper ◽  
Marisa B. Marques ◽  
Rakesh P. Patel

2012 ◽  
Vol 44 (7) ◽  
pp. 1072-1077 ◽  
Author(s):  
Yuki Ogasawara ◽  
Takuya Ohminato ◽  
Yusuke Nakamura ◽  
Kazuyuki Ishii

Transfusion ◽  
2011 ◽  
Vol 51 (7) ◽  
pp. 1439-1449 ◽  
Author(s):  
Sara Rinalducci ◽  
Gian M. D'Amici ◽  
Barbara Blasi ◽  
Stefania Vaglio ◽  
Giuliano Grazzini ◽  
...  

FEBS Open Bio ◽  
2014 ◽  
Vol 4 (1) ◽  
pp. 848-852 ◽  
Author(s):  
Y.I. Ishida ◽  
M. Takikawa ◽  
T. Suzuki ◽  
M. Nagahama ◽  
Y. Ogasawara

2019 ◽  
Vol 518 (4) ◽  
pp. 685-690
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Yo-ichi Ishida ◽  
Yuko Ichinowatari ◽  
Shoichi Nishimoto ◽  
Shin Koike ◽  
Kazuyuki Ishii ◽  
...  

Author(s):  
Kosuke Ueda ◽  
Hiroto Washida ◽  
Nakazo Watari

IntroductionHemoglobin crystals in the red blood cells were electronmicroscopically reported by Fawcett in the cat myocardium. In the human, Lessin revealed crystal-containing cells in the periphral blood of hemoglobin C disease patients. We found the hemoglobin crystals and its agglutination in the erythrocytes in the renal cortex of the human renal lithiasis, and these patients had no hematological abnormalities or other diseases out of the renal lithiasis. Hemoglobin crystals in the human erythrocytes were confirmed to be the first case in the kidney.Material and MethodsTen cases of the human renal biopsies were performed on the operations of the seven pyelolithotomies and three ureterolithotomies. The each specimens were primarily fixed in cacodylate buffered 3. 0% glutaraldehyde and post fixed in osmic acid, dehydrated in graded concentrations of ethanol, and then embedded in Epon 812. Ultrathin sections, cut on LKB microtome, were doubly stained with uranyl acetate and lead citrate.


Author(s):  
John A. Trotter

Hemoglobin is the specific protein of red blood cells. Those cells in which hemoglobin synthesis is initiated are the earliest cells that can presently be considered to be committed to erythropoiesis. In order to identify such early cells electron microscopically, we have made use of the peroxidatic activity of hemoglobin by reacting the marrow of erythropoietically stimulated guinea pigs with diaminobenzidine (DAB). The reaction product appeared as a diffuse and amorphous electron opacity throughout the cytoplasm of reactive cells. The detection of small density increases of such a diffuse nature required an analytical method more sensitive and reliable than the visual examination of micrographs. A procedure was therefore devised for the evaluation of micrographs (negatives) with a densitometer (Weston Photographic Analyzer).


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