Department of Cardiovascular and Renal Research, Institute of Molecular Medicine, University of Southern Denmark, Odense, Denmark.
Section of Molecular Diabetes & Metabolism, Institute of Clinical Research, Steno Diabetes Center Odense, Odense University Hospital, Odense C, Denmark.
Acta Physiol (Oxf). 2020 Jan;228(1):e13346. doi: 10.1111/apha.13346. Epub 2019 Aug 1.
Urinary extracellular vesicles (uEVs) are a heterogenous group of vesicles consisting mainly of microvesicles and exosomes that originate predominantly (99.96%) from kidney, the urinary tract epithelium and the male reproductive tract. Secreted EVs contain molecular cargo from parental cells and provide an attractive source for biomarkers, a potential readout of physiological and pathophysiological mechanisms, and events associated with the urinary system. uEVs are readily enriched and isolated from urine samples and we review 6 standard methods that allow for downstream analysis of the uEV cargo. Although the use of uEVs as a surrogate readout for physiological changes in tissue protein levels is widespread, the protein abundance in uEVs is affected significantly by mechanisms that regulate protein sorting and secretion in uEVs. Data suggest that baseline kidney tissue and uEV levels of apical membrane-associated electrolyte transport proteins are not directly related in human patients. Recent evidence indicates that EVs may contribute to physiological and pathophysiological intercellular signalling and EVs confer protection against renal ischemia-reperfusion injury. The therapeutic use of EVs as information carriers has mainly been explored in vitro and a major hurdle lies in the translation of the in vitro findings into an in vivo setting. Thus, the EV research field is moving from a technical focus to a more physiological focus, allowing for a deeper understanding of human physiology, development of diagnostic tools and potential treatment strategies for precision medicine.
尿细胞外囊泡 (uEVs) 是一类异质性囊泡,主要由微囊泡和外泌体组成,主要来源于肾脏、尿路上皮和男性生殖道。分泌的 EVs 包含来自亲代细胞的分子货物,为生物标志物提供了有吸引力的来源,这是生理和病理生理机制以及与泌尿系统相关事件的潜在读出。uEVs 可从尿液样本中轻易富集和分离,我们综述了 6 种标准方法,这些方法允许对 uEV 货物进行下游分析。尽管将 uEV 用作组织蛋白水平生理变化的替代读出物已被广泛应用,但 uEV 中的蛋白质丰度受到调节 uEV 中蛋白质分拣和分泌的机制的显著影响。有数据表明,在人类患者中,基底肾脏组织和 uEV 水平的顶端膜相关电解质转运蛋白之间没有直接关系。最近的证据表明,EVs 可能有助于生理和病理生理细胞间信号传递,EVs 提供了对肾缺血再灌注损伤的保护。EV 作为信息载体的治疗用途主要在体外进行了探索,主要障碍在于将体外发现转化为体内环境。因此,EV 研究领域正从技术重点转向更注重生理的重点,从而更深入地了解人类生理学,开发诊断工具和精准医学的潜在治疗策略。