Cell Preservation by Application of Tardigrada's Adaptation to Extreme Circumstances

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T. Nemoto ◽  
Tadahiro Kin ◽  
M. Nakano ◽  
A. Shimamoto ◽  
F. Nogata ◽  
...  
Keyword(s):  
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John G. Baust

PLoS ONE ◽  
2013 ◽  
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Bote G. Bruinsma ◽  
Jungwoo Lee ◽  
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2017 ◽  
Vol 69 (11) ◽  
pp. 591
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Brielle Tishler ◽  
Kimberlee Gauvreau ◽  
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Robert J. Howe ◽  
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W.L. Corwin ◽  
J.M. Baust

Blood ◽  
1996 ◽  
Vol 87 (4) ◽  
pp. 1612-1616 ◽  
Author(s):  
UJ Dumaswala ◽  
RU Dumaswala ◽  
DS Levin ◽  
TJ Greenwalt

In earlier studies we have shown that a final concentration of 0.69% glycerol in blood mixed with an experimental additive solution, EAS 25, improves the in vitro quality and in vivo survival of red blood cells (RBCs). The objective of this study was to determine if the better preservation of RBCs in EAS 25 is correlated with the improved maintenance of membrane lipids and proteins and decreased vesiculation. Split units of RBCs were stored in Adsol or EAS 25 (mmol/L: adenine 2/2, dextrose 122/110, mannitol 42/55, glycerol 0/150, NaCl 154/50). After 12 weeks storage, RBC and microvesicle membranes were analyzed for cholesterol, phospholipid, diphenyl hexatriene fluorescence anisotropy, and acetylcholinesterase (AchE) activity. Bands 3 and 4.1 were identified in the microvesicle membranes by immunoblotting. The RBC membrane cholesterol, phospholipids, and AchE remained higher in EAS 25 than in Adsol (P < .001). Vesicle membrane lipids and AchE in EAS 25 were significantly less than in Adsol (P < .001). The fluidity of stored cells in both the solutions was greater than the prestorage samples. Immunoblotting analyses showed that bands 3 and 4.1 were greatly reduced in the microvesicle membranes shed by the RBCs stored in EAS 25 compared with those formed in Adsol.


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