Akbari Shareef, Abou-Arkoub Rima, Sun Suzy, Hiremath Swapnil, Reunov Arkadiy, McCormick Brendan B, Ruzicka Marcel, Burger Dylan
Kidney Research Centre, The Ottawa Hospital Research Institute, University of Ottawa, Ontario, Canada.
Division of Nephrology, The Ottawa Hospital, Ontario, Canada.
Can J Kidney Health Dis. 2017 Mar 22;4:2054358117699829. doi: 10.1177/2054358117699829. eCollection 2017.
Injury to the mesothelial layer of the peritoneal membrane during peritoneal dialysis (PD) is implicated in loss of ultrafiltration capacity, but there are no validated biomarkers for mesothelial cell injury. Microparticles (MPs) are 0.1 to 1.0 µm membrane vesicles shed from the cell surface following injury and are sensitive markers of tissue damage. Formation of MPs in the peritoneal cavity during PD has not been reported to date.
We designed a single-center, proof of concept study to assess whether peritoneal solution exposure induces formation of mesothelial MPs suggestive of PD membrane injury. We examined MP levels in PD effluents by electron microscopy, nanoparticle tracking analysis (NTA), flow cytometry, procoagulant activity, and Western blot.
NTA identified particles in the size range of 30 to 900 nm, with a mean of 240 (SE: 10 nm). MP levels increased in a progressive manner during a 4-hour PD dwell. Electron microscopy confirmed size and morphology of vesicles consistent with characteristics of MPs as well as the presence of mesothelin on the surface. Western blot analysis of the MP fraction also identified the presence of mesothelin after 4 hours, suggesting that MPs found in PD effluents may arise from mesothelial cells.
Our results suggest that MPs are formed and accumulate in the peritoneal cavity during PD, possibly as a stress response. Assessing levels of MPs in PD effluents may be useful as a biomarker for peritoneal membrane damage.
腹膜透析(PD)期间腹膜间皮细胞层损伤与超滤能力丧失有关,但尚无经过验证的间皮细胞损伤生物标志物。微颗粒(MPs)是细胞损伤后从细胞表面脱落的0.1至1.0 µm膜囊泡,是组织损伤的敏感标志物。迄今为止,尚未报道PD期间腹膜腔内MPs的形成情况。
我们设计了一项单中心概念验证研究,以评估腹膜透析液暴露是否会诱导形成提示PD膜损伤的间皮MPs。我们通过电子显微镜、纳米颗粒跟踪分析(NTA)、流式细胞术、促凝活性和蛋白质印迹法检测了PD流出液中的MP水平。
NTA鉴定出大小在30至900 nm范围内的颗粒,平均大小为240(标准误:10 nm)。在4小时的PD驻留期间,MP水平呈逐渐上升趋势。电子显微镜证实了囊泡的大小和形态与MPs的特征一致,并且表面存在间皮素。对MP部分的蛋白质印迹分析也显示4小时后存在间皮素,这表明在PD流出液中发现的MPs可能源自间皮细胞。
我们的结果表明,在PD期间MPs在腹膜腔内形成并积聚,可能是一种应激反应。评估PD流出液中MPs的水平可能作为腹膜膜损伤的生物标志物。