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血液透析导致活性氧生成增加及细胞表面标志物表达增强。

Enhancement of reactive oxygen species production and cell surface markers expression due to haemodialysis.

作者信息

Cristol J P, Canaud B, Rabesandratana H, Gaillard I, Serre A, Mion C

机构信息

Department of Nephrology, Hopital Lapeyronie, Montpellier, France.

出版信息

Nephrol Dial Transplant. 1994;9(4):389-94.

PMID:8084452
Abstract

Leukocyte activation during haemodialysis (HD) was evaluated by reactive oxygen species (ROS) production and cell surface markers expression (CD11b: C3bi receptor and CD25: IL2 receptor). Eight end-stage renal disease patients were exposed to three dialysis phases according to a A/B/A protocol study. During phase A polysulphone (PS) membranes were used and during phase B cuprophane (CU) membranes were used. Each phase lasted 3 weeks. Timed samples were collected during the last session of each phase at 0, 15, and 30 min of HD. Flow cytometry analysis was performed both on monocytes (MO), polymorphonuclears (PMN), and lymphocytes (Ly). Hydroethydine was used as a marker of cell-ROS production. Specific monoclonal antibodies were used to analyse the cell surface markers. CU increased ROS production in PMN and MO by 10- and 2.4-fold respectively and had no significant effect on Ly. CU enhanced 16-fold CD11b expression on PMN, and increased also CD11b and CD25 expression on MO by 7- and 40-fold respectively. On the contrary, PS did not affect either ROS production or cell surface markers expression in MO, PMN, Ly. We conclude that oxydative metabolism and cell surface markers expression of PMN and MO were significantly increased with cuprophane membranes and not with polysulphone membranes, suggesting that complex cell-cell interactions were involved in membrane-related bioincompatibility phenomena.

摘要

通过活性氧(ROS)生成和细胞表面标志物表达(CD11b:C3bi受体和CD25:IL2受体)评估血液透析(HD)期间的白细胞活化。根据A/B/A方案研究,八名终末期肾病患者经历了三个透析阶段。在A阶段使用聚砜(PS)膜,在B阶段使用铜仿(CU)膜。每个阶段持续3周。在每个阶段的最后一次透析过程中,于HD开始后的0、15和30分钟采集定时样本。对单核细胞(MO)、多形核细胞(PMN)和淋巴细胞(Ly)进行流式细胞术分析。氢乙锭用作细胞ROS生成的标志物。使用特异性单克隆抗体分析细胞表面标志物。CU使PMN和MO中的ROS生成分别增加了10倍和2.4倍,对Ly没有显著影响。CU使PMN上的CD11b表达增强了16倍,还使MO上的CD11b和CD25表达分别增加了7倍和40倍。相反,PS对MO、PMN、Ly中的ROS生成或细胞表面标志物表达均无影响。我们得出结论,铜仿膜可显著增加PMN和MO的氧化代谢及细胞表面标志物表达,而聚砜膜则无此作用,这表明复杂的细胞间相互作用参与了与膜相关的生物不相容现象。

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