Extracellular vesicle-bound DNA in urine is indicative of kidney allograft injury

Ivana Sedej, Maja Štalekar, Magda Tušek Žnidarič, Katja Goričar, Nika Kojc, Polona Kogovšek, Vita Dolžan, Miha Arnol, Metka Lenassi
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Abstract

Extracellular vesicle-bound DNA (evDNA) is an understudied extracellular vesicle (EV) cargo, particularly in cancer-unrelated fundamental and biomarker research. Although evDNA has been detected in urine, little is known about its characteristics, localization, and biomarker potential for kidney pathologies. To address this, we enriched EVs from urine of well-characterized kidney transplant recipients undergoing allograft biopsy, characterized their evDNA and its association to allograft injury. Using DNase treatment and immunogold labelling TEM, we show that DNA is bound to the surface of urinary EVs. Although the urinary evDNA and cell-free DNA correlated in several characteristics, the DNA integrity index showed evDNA was less fragmented (P < 0.001). Urinary EVs from patients with rejection and non-rejection allograft injury were significantly larger (mean: P = 0.045, median: P = 0.031) and have bound more DNA as measured by normalized evDNA yield (P = 0.018) and evDNA copy number (P = 0.007), compared to patients with normal histology. Urinary evDNA characteristics associated with the degree of interstitial inflammation, combined glomerulitis and peritubular capillaritis, and inflammation in areas of fibrosis (all P < 0.050). The normalized dd-evDNA copy numbers differed between the antibody- and T cell-mediated rejection (P = 0.036). Our study supports the importance of DNA as urine EV cargo, especially as potential non-invasive kidney allograft injury biomarker.
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尿中细胞外囊泡结合DNA提示同种异体肾移植损伤
细胞外囊泡结合DNA (evDNA)是一种未被充分研究的细胞外囊泡(EV)货物,特别是在与癌症无关的基础和生物标志物研究中。尽管evDNA已在尿液中检测到,但对其特征、定位和肾脏病变的生物标志物潜力知之甚少。为了解决这个问题,我们从接受同种异体移植活检的肾移植受者的尿液中富集EVs,表征他们的evDNA及其与同种异体移植损伤的关系。通过DNA酶处理和免疫金标记TEM,我们发现DNA与尿ev表面结合。尽管尿液evDNA与无细胞DNA在多个特征上存在相关性,但DNA完整性指数显示evDNA片段化程度较低(P <0.001)。排斥反应和非排斥反应同种异体移植损伤患者的尿EVs明显大于正常组织的患者(平均:P = 0.045,中位数:P = 0.031),并且通过标准化evDNA产率(P = 0.018)和evDNA拷贝数(P = 0.007)来测量EVs结合更多的DNA。尿evDNA特征与间质性炎症程度、合并肾小球炎和小管周围毛细血管炎以及纤维化区炎症相关(所有P <0.050)。标准化的dd-evDNA拷贝数在抗体和T细胞介导的排斥反应中存在差异(P = 0.036)。我们的研究支持DNA作为尿液EV货物的重要性,特别是作为潜在的非侵入性肾移植损伤生物标志物。
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