Remote Ischemic Preconditioning (RIPC) Modifies Plasma Proteome in Humans

被引:63
|
作者
Hepponstall, Michele [1 ,2 ,3 ,4 ]
Ignjatovic, Vera [1 ,3 ]
Binos, Steve [4 ]
Monagle, Paul [1 ,3 ]
Jones, Bryn [1 ,2 ]
Cheung, Michael H. H. [1 ,2 ,3 ]
d'Udekem, Yves [1 ,2 ]
Konstantinov, Igor E. [1 ,2 ,3 ]
机构
[1] Murdoch Childrens Res Inst, Melbourne, Vic, Australia
[2] Royal Childrens Hosp, Cardiac Surg Unit & Cardiol, Melbourne, Vic, Australia
[3] Univ Melbourne, Dept Paediat, Melbourne, Vic, Australia
[4] Dept Primary Ind, Biosci Res Div, Melbourne, Vic, Australia
来源
PLOS ONE | 2012年 / 7卷 / 11期
基金
英国医学研究理事会;
关键词
COMPLEMENT GENE-EXPRESSION; HIGH-DENSITY-LIPOPROTEIN; REPERFUSION INJURY; ISCHEMIA/REPERFUSION INJURY; PEPTIDE B-BETA(15-42); MYOCARDIAL-INFARCTION; DEPENDENT MECHANISM; CARDIAC-SURGERY; PROTECTION; TISSUE;
D O I
10.1371/journal.pone.0048284
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Remote Ischemic Preconditioning (RIPC) induced by brief episodes of ischemia of the limb protects against multi-organ damage by ischemia-reperfusion (IR). Although it has been demonstrated that RIPC affects gene expression, the proteomic response to RIPC has not been determined. This study aimed to examine RIPC induced changes in the plasma proteome. Five healthy adult volunteers had 4 cycles of 5 min ischemia alternating with 5 min reperfusion of the forearm. Blood samples were taken from the ipsilateral arm prior to first ischaemia, immediately after each episode of ischemia as well as, at 15 min and 24 h after the last episode of ischemia. Plasma samples from five individuals were analysed using two complementary techniques. Individual samples were analysed using 2Dimensional Difference in gel electrophoresis (2D DIGE) and mass spectrometry (MS). Pooled samples for each of the time-points underwent trypsin digestion and peptides generated were analysed in triplicate using Liquid Chromatography and MS (LC-MS). Six proteins changed in response to RIPC using 2D DIGE analysis, while 48 proteins were found to be differentially regulated using LC-MS. The proteins of interest were involved in acute phase response signalling, and physiological molecular and cellular functions. The RIPC stimulus modifies the plasma protein content in blood taken from the ischemic arm in a cumulative fashion and evokes a proteomic response in peripheral blood.
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页数:11
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