Department of Internal Medicine, University Tor Vergata, Via Montpellier 1, Rome, Italy.
Blood Transfus. 2012 May;10 Suppl 2(Suppl 2):s101-12. doi: 10.2450/2012.014S.
During haemodialysis procedure, the contact of blood with the membrane material contained in the hemodialyser results in protein deposition and adsorption, and surface-adsorbed proteins may trigger a variety of biological pathways with potential pathophysiologic consequences. The present work was undertaken to examine for protein adsorption capacity of two membranes used for clinical haemodialysis, namely cellulose triacetate (a derivatized cellulosic membrane) and the synthetic polymer polysulfone-based helixone.
We performed a prospective cross-over study in chronic haemodialysis patients, routinely treated with a cellulose triacetate dialyser (n=3) or with a helixone dialyser (n=3). Dialysers from each patient were obtained after dialysis session, and flushed with a litre of saline to remove residual blood. Adsorbed proteins were then eluted by a strong chaotropic buffer. Patients were next switched to the other membrane dialyser for four weeks, at the end of this period protein adsorption being evaluated again. After silver staining, expression profile protein of the two groups was analyzed by 2-DE gels, analyzed and identified by Peptide Mass-finger printing and MALDI-TOF-MS/MS sequency. Moreover nanoLC-MS/MS shotgun profiling was pursued using a semi-quantitative label free approach by emPAI data analysis.
A total of 54 differentially expressed proteins were identified: 22 proteins more concentrated in helixone membrane (predominantly low abundant plasma proteins) and 32 in cellulose triacetate (most represented by high abundant plasma proteins). The difference proved to be related to membrane material and not to patient's characteristics.
Proteomic techniques represent a useful approach for the investigation of proteins surface-adsorbed onto a haemodialysis membrane, and can also be applied for critical assessment to compare efficiencies of different dialyser membrane materials in the adsorption of plasma proteins.
在血液透析过程中,血液与血液透析器中包含的膜材料接触会导致蛋白质沉积和吸附,而表面吸附的蛋白质可能会触发多种具有潜在病理生理后果的生物学途径。本研究旨在检测两种用于临床血液透析的膜的蛋白质吸附能力,即醋酸纤维素(衍生纤维素膜)和基于合成聚合物聚砜的螺旋one。
我们对常规使用醋酸纤维素透析器(n=3)或螺旋 one 透析器(n=3)进行治疗的慢性血液透析患者进行了前瞻性交叉研究。从每位患者中取出透析器,并用 1 升生理盐水冲洗以清除残留血液。然后用强离子变性缓冲液洗脱吸附的蛋白质。患者随后切换到另一种膜透析器四周,在此期间结束后再次评估蛋白质吸附。经过银染后,通过 2-DE 凝胶分析两组的蛋白质表达谱,通过肽质量指纹图谱和 MALDI-TOF-MS/MS 测序进行分析和鉴定。此外,还使用半定量无标记方法通过 emPAI 数据分析进行了 nanoLC-MS/MS shotgun profiling。
共鉴定出 54 种差异表达蛋白:22 种蛋白在螺旋 one 膜中更集中(主要是低丰度血浆蛋白),32 种蛋白在醋酸纤维素中更集中(主要是高丰度血浆蛋白)。这种差异与膜材料有关,与患者特征无关。
蛋白质组学技术是研究血液透析膜表面吸附蛋白质的有用方法,也可用于比较不同透析器膜材料在血浆蛋白吸附方面的效率。