Circulating extracellular vesicles as a potential source of new biomarkers of drug-induced liver injury

被引:39
作者
Yang, Xi [1 ]
Weng, Zuquan [1 ]
Mendrick, Donna L. [1 ]
Shi, Qiang [1 ]
机构
[1] Food & Drug Adm, Div Syst Biol, Natl Ctr Toxicol Res, Jefferson, AR 72079 USA
关键词
Drug-induced liver injury; Biomarkers; Extracellular vesicles; Exosomes; MESSENGER-RNAS; MICRORNA PROFILES; EXOSOME ISOLATION; HEPATOTOXICITY; PLASMA; IDENTIFICATION; BLOOD; RATS; MICROVESICLES; INDIVIDUALS;
D O I
10.1016/j.toxlet.2014.01.013
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Like most cell types, hepatocytes constantly produce extracellular vesicles (EVs) such as exosomes and microvesicles that are released into the circulation to transport signaling molecules and cellular waste. Circulating EVs are being vigorously explored as biomarkers of diseases and toxicities, including drug-induced liver injury (DILI). Emerging data suggest that (a) blood-borne EVs contain liver-specific mRNAs and microRNAs (miRNAs), (b) the levels can be remarkably elevated in response to DILI, and (c) the increases correlate well with classical measures of liver damage. The expression profile of mRNAs in EVs and the compartmentalization of miRNAs within EVs or other blood fractions were found to be indicative of the offending drug involved in DILI, thus providing more informative assessment of liver injury than using alanine aminotransferase alone. EVs in the urine and cell culture medium were also found to contain proteins or mRNAs that were indicative of DILI. However, major improvements in EV isolation methods are needed for the discovery, evaluation, and quantification of possible DILI biomarkers in circulating EVs. Published by Elsevier Ireland Ltd.
引用
收藏
页码:401 / 406
页数:6
相关论文
共 56 条
[51]   Quantitative Analyses and Transcriptomic Profiling of Circulating Messenger RNAs as Biomarkers of Rat Liver Injury [J].
Wetmore, Barbara A. ;
Brees, Dominique J. ;
Singh, Reetu ;
Watkins, Paul B. ;
Andersen, Melvin E. ;
Loy, James ;
Thomas, Russell S. .
HEPATOLOGY, 2010, 51 (06) :2127-2139
[52]   Standardization of sample collection, isolation and analysis methods in extracellular vesicle research [J].
Witwer, Kenneth W. ;
Buzas, Edit I. ;
Bemis, Lynne T. ;
Bora, Adriana ;
Lasser, Cecilia ;
Lotvall, Jan ;
Hoen, Esther N. Nolte-'t ;
Piper, Melissa G. ;
Sivaraman, Sarada ;
Skog, Johan ;
Thery, Clotilde ;
Wauben, Marca H. ;
Hochberg, Fred .
JOURNAL OF EXTRACELLULAR VESICLES, 2013, 2 (01)
[53]   Cellular imaging predictions of clinical drug-induced liver injury [J].
Xu, Jinghai J. ;
Henstock, Peter V. ;
Dunn, Margaret C. ;
Smith, Arthur R. ;
Chabot, Jeffrey R. ;
de Graaf, David .
TOXICOLOGICAL SCIENCES, 2008, 105 (01) :97-105
[54]   Plasma MicroRNA Profiles in Rat Models of Hepatocellular Injury, Cholestasis, and Steatosis [J].
Yamaura, Yu ;
Nakajima, Miki ;
Takagi, Shingo ;
Fukami, Tatsuki ;
Tsuneyama, Koichi ;
Yokoi, Tsuyoshi .
PLOS ONE, 2012, 7 (02)
[55]   Identification of Urinary microRNA Profiles in Rats That May Diagnose Hepatotoxicity [J].
Yang, Xi ;
Greenhaw, James ;
Shi, Qiang ;
Su, Zhenqiang ;
Qian, Feng ;
Davis, Kelly ;
Mendrick, Donna L. ;
Salminen, William F. .
TOXICOLOGICAL SCIENCES, 2012, 125 (02) :335-344
[56]   Predose Blood Gene Expression Profiles Might Identify the Individuals Susceptible to Carbon Tetrachloride-Induced Hepatotoxicity [J].
Yun, Jun-Won ;
Lee, Tae-Ryong ;
Kim, Chae-Wook ;
Park, Young-Ho ;
Chung, Jin-Ho ;
Lee, Yong-Soon ;
Kang, Kyung-Sun ;
Lim, Kyung-Min .
TOXICOLOGICAL SCIENCES, 2010, 115 (01) :12-21