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Effect of a glycerol-containing hypotonic medium on erythrocyte phospholipid asymmetry and aminophospholipid transport during storage

机译:储存过程中含甘油的低渗介质对红细胞磷脂不对称性和氨基磷脂转运的影响

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Previous studies from our laboratory have shown that under blood bank storage conditions red blood cell (RBC) ATP and lipid content were better maintained in a glycerol-containing hypotonic experimental additive solution (EAS 25) than in the conventional storage medium Adsola. The objective of this study was to determine the mechanism of the protective effect of EAS 25, by measuring transmembrane phospholipid asymmetry and the membrane integrity of stored RBCs. Split units of packed RBCs were stored in either EAS 25 or Adsol?. RBCs were analyzed after 0, 42, and 84 days and vesicles shed from stored RBCs were analyzed after 84 days of storage. Phospholipid asymmetry was measured by phospholipase A2 digestion (RBCs) and activation of the prothrombinase complex (RBCs, vesicles). RBC membrane exhibited a significantly greater (P < 0.01) amount of phosphatidylethanolamine externalized after storage in Adsol? than in EAS 25 (44.3% ± 11.7 vs. 25.3% ± 5.7, respectively). Prothrombin converting activities in RBCs were significantly lower than in shed vesicles (P < 0.001) suggesting the presence of phosphatidylserine in the outer monolayer of vesicle, but not in RBC membranes. The rates of inwardly-directed aminophospholipid transport in RBCs decreased by 50% and glutathione levels decreased by ≈ 50% in both media. RBC cholesterol and phospholipid content of stored RBCs remained significantly greater (P > 0.01) in EAS 25 than in Adsole. The results indicate that despite comparable reduction in the rate of aminophospholipid transport and reduced GSH concentrations, RBC phospholipid asymmetry was better maintained during storage in EAS 25 than in Adsol. The data suggest that glycerol in the hypotonic EAS helps preserve RBC lipid organization and membrane integrity during storage.
机译:我们实验室的先前研究表明,在血库储存条件下,含甘油的低渗实验添加剂溶液(EAS 25)中的红细胞(RBC)ATP和脂质含量比传统的储存介质Adsola更好。这项研究的目的是通过测量跨膜磷脂的不对称性和所储存的RBC的膜完整性来确定EAS 25的保护作用机理。包装好的RBC的拆分单位存储在EAS 25或Adsol?中。在0、42和84天后分析RBC,并且在储存84天后分析从储存的RBC中脱落的囊泡。通过磷脂酶A2消化(RBC)和凝血酶原酶复合物(RBCs,囊泡)的活化来测量磷脂的不对称性。储存在Adsol?中后,RBC膜表现出明显更多(P <0.01)的磷脂酰乙醇胺外化量。相比EAS 25(分别为44.3%±11.7和25.3%±5.7)。 RBC中的凝血酶原转化活性显着低于脱落的囊泡(P <0.001),表明在囊泡的外单层中存在磷脂酰丝氨酸,但在RBC膜中则没有。在两种介质中,RBC中向内定向的氨基磷脂转运率降低了50%,谷胱甘肽水平降低了约50%。 EAS 25中储存的RBC中的RBC胆固醇和磷脂含量仍显着高于Adsole(P> 0.01)。结果表明,尽管氨基磷脂转运速率降低和GSH浓度降低相当,但在EAS 25中储存的RBC磷脂不对称性要比在Adsol中更好。数据表明低渗EAS中的甘油有助于在储存过程中保持RBC脂质组织和膜完整性。

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