Urinary Extracellular Vesicle: A Potential Source of Early Diagnostic and Therapeutic Biomarker in Diabetic Kidney Disease

被引:21
作者
Xu, Wei-Cheng [1 ]
Qian, Ge [1 ]
Liu, Ai-Qun [1 ]
Li, Yong-Qiang [1 ]
Zou, He-Qun [1 ]
机构
[1] Southern Med Univ, Inst Nephrol & Urol, Affiliated Hosp 3, Dept Nephrol, Guangzhou 510630, Guangdong, Peoples R China
关键词
Biomarker; Diabetic Kidney Disease; Diagnosis; Extracellular Vesicles; Therapy; DIPEPTIDYL-PEPTIDASE-IV; EXOSOME-LIKE VESICLES; TGF-BETA; EXOSOMES/MICROVESICLES; ULTRAFILTRATION; NEPHROPATHY; PROSTASOMES; BIOGENESIS; EXPRESSION; MATURATION;
D O I
10.4103/0366-6999.232801
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Diabetic kidney disease (DKD) has become one of the major causes of end-stage renal disease. Urinary extracellular vesicles (uEVs) contain rich biological information which could be the ideal source for noninvasive biomarkers of DKD. This review discussed the potential early diagnostic and therapeutic values of proteins and microRNAs in uEVs in DKD. Data Sources: This review was based articles published in PubMed, Embase, Cochrane, and Google Scholar databases up to November 20, 2017, with the following keywords: "Diabetic kidney disease", "Extracellular vesicle", and "Urine". Study Selection: Relevant articles were carefully reviewed, with no exclusions applied to the study design and publication type. Results: There is no "gold standard" technology to separate and/or purify uEVs. The uEVs contain a variety of proteins and RNAs and participate in the physiological and pathological processes of the kidney. UEVs, especially urinary exosomes, may be useful biomarkers for early diagnosis and treatment to DKD. Furthermore, the uEVs has been used as a therapeutic target for DKD. Conclusion: Proteins and nucleic acids in uEVs represent promising biomarker for the diagnosis and treatment of DKD.
引用
收藏
页码:1357 / 1364
页数:8
相关论文
共 84 条
[81]   Urinary exosomal Wilms' tumor-1 as a potential biomarker for podocyte injury [J].
Zhou, Hua ;
Kajiyama, Hiroshi ;
Tsuji, Takayuki ;
Hu, Xuzhen ;
Leelahavanichkul, Asada ;
Vento, Suzanne ;
Frank, Rachel ;
Kopp, Jeffrey B. ;
Trachtman, Howard ;
Star, Robert A. ;
Yuen, Peter S. T. .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2013, 305 (04) :F553-F559
[82]   Mediators of diabetic renal disease:: The case for TGF-β as the major mediator [J].
Ziyadeh, FN .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2004, 15 (01) :S55-S57
[83]   Kidney tissue proteomics reveals regucalcin downregulation in response to diabetic nephropathy with reflection in urinary exosomes [J].
Zubiri, Irene ;
Posada-Ayala, Maria ;
Benito-Martin, Alberto ;
Maroto, Aroa S. ;
Martin-Lorenzo, Marta ;
Cannata-Ortiz, Pablo ;
de la Cuesta, Fernando ;
Gonzalez-Calero, Laura ;
Barderas, Maria G. ;
Fernandez-Fernandez, Beatriz ;
Ortiz, Alberto ;
Vivanco, Fernando ;
Alvarez-Llamas, Gloria .
TRANSLATIONAL RESEARCH, 2015, 166 (05) :474-484
[84]   Diabetic nephropathy induces changes in the proteome of human urinary exosomes as revealed by label-free comparative analysis [J].
Zubiri, Irene ;
Posada-Ayala, Maria ;
Sanz-Maroto, Aroa ;
Calvo, Enrique ;
Martin-Lorenzo, Marta ;
Gonzalez-Calero, Laura ;
de la Cuesta, Fernando ;
Lopez, Juan A. ;
Fernandez-Fernandez, Beatriz ;
Ortiz, Alberto ;
Vivanco, Fernando ;
Alvarez-Llamas, Gloria .
JOURNAL OF PROTEOMICS, 2014, 96 :92-102