Perez-Hernandez Javier, Forner Maria J, Pinto Carolina, Chaves Felipe J, Cortes Raquel, Redon Josep
Genotyping and Genetic Diagnosis Unit, INCLIVA Biomedical Research Institute, Valencia, Spain; Cardiometabolic and Renal Unit, INCLIVA Biomedical Research Institute, Valencia, Spain.
Cardiometabolic and Renal Unit, INCLIVA Biomedical Research Institute, Valencia, Spain; CIBER Physiopathology of Obesity and Nutrition (CIBEROBN), Institute of Health Carlos III, Minister of Health, Madrid, Spain.
PLoS One. 2015 Sep 21;10(9):e0138618. doi: 10.1371/journal.pone.0138618. eCollection 2015.
There is increased interest in using microRNAs (miRNAs) as biomarkers in different diseases. Present in body fluids, it is controversial whether or not they are mainly enclosed in exosomes, thus we studied if urinary miRNAs are concentrated inside exosomes and if the presence of systemic lupus erythematosus with or without lupus nephritis modifies their distribution pattern. We quantified specific miRNAs in urine of patients with systemic lupus erythematosus (n = 38) and healthy controls (n = 12) by quantitative reverse-transcription PCR in cell-free urine, exosome-depleted supernatant and exosome pellet obtained by ultracentrifugation. In control group, miR-335* and miR-302d were consistently higher in exosomes than in exosome-depleted supernatant, and miR-200c and miR-146a were higher in cell-free fraction. In lupus patients, all urinary miRNAs tested were mainly in exosomes with lower levels outside them (p<0.05 and p<0.01, respectively). This pattern is especially relevant in patients with active lupus nephritis compared to the control group or to the SLE patients in absence of lupus nephritis, with miR-146a being the most augmented (100-fold change, p<0.001). Among the exosomal miRNAs tested, only the miR-146a discriminates the presence of active lupus nephritis. In conclusion, urinary miRNAs are contained primarily in exosomes in systemic lupus erythematosus, and the main increment was found in the presence of active lupus nephritis. These findings underscore the attractiveness of exosomal miRNAs in urine, a non-invasive method, as potential renal disease markers.
将微小RNA(miRNA)用作不同疾病的生物标志物正受到越来越多的关注。miRNA存在于体液中,它们是否主要包裹在外泌体中仍存在争议,因此我们研究了尿液中的miRNA是否在外泌体中富集,以及系统性红斑狼疮伴或不伴狼疮性肾炎是否会改变其分布模式。我们通过定量逆转录PCR对系统性红斑狼疮患者(n = 38)和健康对照者(n = 12)尿液中的游离尿液、去除外泌体的上清液和通过超速离心获得的外泌体沉淀中的特定miRNA进行了定量。在对照组中,miR-335*和miR-302d在外泌体中的含量始终高于去除外泌体的上清液,而miR-200c和miR-146a在游离部分中含量更高。在狼疮患者中,所有检测的尿液miRNA主要存在于外泌体中,其外部水平较低(分别为p<0.05和p<0.01)。与对照组或无狼疮性肾炎的系统性红斑狼疮患者相比,这种模式在活动性狼疮性肾炎患者中尤为明显,其中miR-146a增加最为显著(变化100倍,p<0.001)。在所检测的外泌体miRNA中,只有miR-146a能够区分活动性狼疮性肾炎的存在。总之,系统性红斑狼疮患者尿液中的miRNA主要包含在外泌体中,并且在活动性狼疮性肾炎患者中发现其含量主要增加。这些发现强调了尿液中外泌体miRNA作为潜在肾脏疾病标志物的吸引力,尿液检测是一种非侵入性方法。