Urinary Exosomal MicroRNAs in Incipient Diabetic Nephropathy

被引:275
作者
Barutta, Federica [1 ]
Tricarico, Marinella [1 ]
Corbelli, Alessandro [2 ,3 ,4 ]
Annaratone, Laura [5 ]
Pinach, Silvia [1 ]
Grimaldi, Serena [1 ]
Bruno, Graziella [1 ]
Cimino, Daniela [6 ]
Taverna, Daniela [6 ]
Deregibus, Maria Chiara [7 ]
Rastaldi, Maria Pia
Perin, Paolo Cavallo [1 ]
Gruden, Gabriella [1 ]
机构
[1] Univ Turin, Dept Med Sci, Diabet Nephropathy Lab, Turin, Italy
[2] Osped Maggiore Policlin, Fdn IRCCS, Renal Res Lab, Milan, Italy
[3] Fdn DAmico Ric Malattie Renali, Milan, Italy
[4] Milano Bicocca Univ, MIA Consortium Image Anal, Milan, Italy
[5] Univ Turin, Dept Biomed Sci & Human Oncol, I-10124 Turin, Italy
[6] Univ Turin, Ctr Mol Biotechnol, Turin, Italy
[7] Univ Turin, Dept Med Sci, Lab Renal & Vasc Pathophysiol, Turin, Italy
来源
PLOS ONE | 2013年 / 8卷 / 11期
关键词
KIDNEY GLOMERULI; EXPRESSION; CELLS; MICROALBUMINURIA; TGF-BETA-1; MIR-145; PLASMA;
D O I
10.1371/journal.pone.0073798
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
MicroRNAs (miRNAs), a class of small non-protein-encoding RNAs, regulate gene expression via suppression of target mRNAs. MiRNAs are present in body fluids in a remarkable stable form as packaged in microvesicles of endocytic origin, named exosomes. In the present study, we have assessed miRNA expression in urinary exosomes from type 1 diabetic patients with and without incipient diabetic nephropathy. Results showed that miR-130a and miR-145 were enriched, while miR-155 and miR-424 reduced in urinary exosomes from patients with microalbuminuria. Similarly, in an animal model of early experimental diabetic nephropathy, urinary exosomal miR-145 levels were increased and this was paralleled by miR-145 overexpression within the glomeruli. Exposure of cultured mesangial cells to high glucose increased miR-145 content in both mesangial cells and mesangial cells-derived exosomes, providing a potential mechanism for diabetes-induced miR-145 overexpression. In conclusion, urinary exosomal miRNA content is altered in type 1 diabetic patients with incipient diabetic nephropathy and miR-145 may represent a novel candidate biomarker/player in the complication.
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页数:8
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共 39 条
  • [31] Role of microRNAs in diabetes and its cardiovascular complications
    Shantikumar, Saran
    Caporali, Andrea
    Emanueli, Costanza
    [J]. CARDIOVASCULAR RESEARCH, 2012, 93 (04) : 583 - 593
  • [32] Exosomes: proteomic insights and diagnostic potential
    Simpson, Richard J.
    Lim, Justin W. E.
    Moritz, Robert L.
    Mathivanan, Suresh
    [J]. EXPERT REVIEW OF PROTEOMICS, 2009, 6 (03) : 267 - 283
  • [33] Surrogate end points for clinical trials of kidney disease progression
    Stevens, Lesley A.
    Greene, Tom
    Levey, Andrew S.
    [J]. CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2006, 1 (04): : 874 - 884
  • [34] A new method for large scale isolation of kidney glomeruli from mice
    Takemoto, M
    Asker, N
    Gerhardt, H
    Lundkvist, A
    Johansson, BR
    Saito, Y
    Betsholtz, C
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 2002, 161 (03) : 799 - 805
  • [35] Down-Regulation of miR-92 in Human Plasma Is a Novel Marker for Acute Leukemia Patients
    Tanaka, Masami
    Oikawa, Kosuke
    Takanashi, Masakatsu
    Kudo, Motoshige
    Ohyashiki, Junko
    Ohyashiki, Kazuma
    Kuroda, Masahiko
    [J]. PLOS ONE, 2009, 4 (05):
  • [36] Effect of the Monocyte Chemoattractant Protein-1/CC Chemokine Receptor 2 System on Nephrin Expression in Streptozotocin-Treated Mice and Human Cultured Podocytes
    Tarabra, Elena
    Giunti, Sara
    Barutta, Federica
    Salvidio, Gennaro
    Burt, Davina
    Deferrari, Giacomo
    Gambino, Roberto
    Vergola, Daniela
    Pinach, Silvia
    Perin, Paolo Cavallo
    Camussi, Giovanni
    Gruden, Gabriella
    [J]. DIABETES, 2009, 58 (09) : 2109 - 2118
  • [37] Exosomes and the kidney: prospects for diagnosis and therapy of renal diseases
    van Balkom, Bas W. M.
    Pisitkun, Trairak
    Verhaar, Marianne C.
    Knepper, Mark A.
    [J]. KIDNEY INTERNATIONAL, 2011, 80 (11) : 1138 - 1145
  • [38] Quantification of gene expression in urinary sediment for the study of renal diseases
    Wang, Gang
    Szeto, Cheuk-Chun
    [J]. NEPHROLOGY, 2007, 12 (05) : 494 - 499
  • [39] Yevdokimova N, 2001, J AM SOC NEPHROL, V12, P703, DOI 10.1681/ASN.V124703