Exosomes: proteomic insights and diagnostic potential

被引:479
作者
Simpson, Richard J. [1 ,2 ]
Lim, Justin W. E. [1 ,2 ]
Moritz, Robert L. [3 ]
Mathivanan, Suresh [1 ,2 ]
机构
[1] Royal Melbourne Hosp, Ludwig Inst Canc Res, Joint Prote Lab JPSL, Parkville, Vic 3050, Australia
[2] Royal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Parkville, Vic 3050, Australia
[3] Inst Syst Biol, Seattle, WA 98103 USA
关键词
exosome; microvesicle; proteomics; CELL-DERIVED-EXOSOMES; ELECTRON-TRANSFER DISSOCIATION; HUMAN A33 ANTIGEN; COMPLEX CLASS-II; MEMBRANE MICROPARTICLES; BIOLOGICAL SIGNIFICANCE; PROTEIN IDENTIFICATION; MULTIVESICULAR BODIES; TRANSFERRIN RECEPTOR; GEL-ELECTROPHORESIS;
D O I
10.1586/EPR.09.17
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Exosomes are 40-100-nm diameter membrane vesicles of endocytic origin that are released by most cell types upon fusion of multivesicular bodies with the plasma membrane, presumably as a vehicle for cell-free intercellular communication. While early studies focused on their secretion from diverse cell types in vitro, exosomes have now been identified in body fluids such as urine, amniotic fluid, malignant ascites, bronchoalveolar lavage fluid, synovial fluid, breast milk, saliva and blood. Exosomes have pleiotropic biological functions, including immune response, antigen presentation, intracellular communication and the transfer of RNA and proteins. While they have also been implicated in the transport and propagation of infectious cargo, such as prions, and retroviruses, including HIV, suggesting a role in pathological situations, recent studies suggest that the presence of such infectious cargo may be artefacts of exosome-purification strategies. Improvements in mass spectrometry-based proteomic tools, both hardware and software, coupled with improved purification schemes for exosomes, has allowed more in-depth proteome analyses, contributing immensely to our understanding of the molecular composition of exosomes. Proteomic cataloguing of exosomes from diverse cell types has revealed a common set of membrane and cytosolic proteins, suggesting the evolutionary importance of these membrane particles. Additionally, exosomes express an array of proteins that reflect the originating host cell. Recent findings that exosomes contain inactive forms of both mRNA and microRNA that can be transferred to another cell and be functional in that new environment, have initiated many microRNA profiling studies of exosomes circulating in blood. These studies highlight the potential of exosomal microRNA profiles for use as diagnostic biomarkers of disease through a noninvasive blood test. The exacerbated release of exosomes in tumor cells, as evidenced by their increased levels in blood during the late stage of a disease and their overexpression of certain tumor cell biomarkers, suggests an important role of exosomes in diagnosis and biomarker studies. The aim of this article is to provide a brief overview of exosomes, including methods used to isolate and characterize exosomes. New advances in proteomic methods, and both mass spectrometry hardware and informatics tools will be covered briefly.
引用
收藏
页码:267 / 283
页数:17
相关论文
共 140 条
[1]   Exosomes with major histocompatibility complex class II and co-stimulatory molecules are present in human BAL fluid [J].
Admyre, C ;
Grunewald, J ;
Thyberg, J ;
Gripenbäck, S ;
Tornling, G ;
Eklund, A ;
Scheynius, A ;
Gabrielsson, S .
EUROPEAN RESPIRATORY JOURNAL, 2003, 22 (04) :578-583
[2]   Exosomes with immune modulatory features are present in human breast milk [J].
Admyre, Charlotte ;
Johansson, Sara M. ;
Qazi, Khaleda Rahman ;
Filen, Jan-Jonas ;
Lahesmaa, Riitta ;
Norman, Mikael ;
Neve, Etienne P. A. ;
Scheynius, Annika ;
Gabrielsson, Susanne .
JOURNAL OF IMMUNOLOGY, 2007, 179 (03) :1969-1978
[3]   Mast cell-derived exosomes activate endothelial cells to secrete plasminogen activator inhibitor type 1 [J].
Al-Nedawi, K ;
Szemraj, J ;
Cierniewski, CS .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2005, 25 (08) :1744-1749
[4]   microRNAs: Tiny regulators with great potential [J].
Ambros, V .
CELL, 2001, 107 (07) :823-826
[5]   TSAP6 facilitates the secretion of translationally controlled tumor protein/histamine-releasing factor via a nonclassical pathway [J].
Amzallag, N ;
Passer, BJ ;
Allanic, D ;
Segura, E ;
Théry, C ;
Goud, B ;
Amson, R ;
Telerman, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (44) :46104-46112
[6]  
ANDERSON DF, 2002, INT J COMMUTATIVE RI, V1, P11
[7]   Quantitative mass spectrometric multiple reaction monitoring assays for major plasma proteins [J].
Anderson, L ;
Hunter, CL .
MOLECULAR & CELLULAR PROTEOMICS, 2006, 5 (04) :573-588
[8]   Malignant effusions and immunogenic tumour-derived exosomes [J].
Andre, F ;
Schartz, NEC ;
Movassagh, M ;
Flament, C ;
Pautier, P ;
Morice, P ;
Pomel, C ;
Lhomme, C ;
Escudier, B ;
Le Chevalier, T ;
Tursz, T ;
Amigorena, S ;
Raposo, G ;
Angevin, E ;
Zitvogel, L .
LANCET, 2002, 360 (9329) :295-305
[9]   RETRACTED: Identification and characterization of microvesicles secreted by 3T3-L1 adipocytes: redox- and Hormone Dependent induction of milk fat globule-epidermal growth factor 8-associated microvesicles (Retracted article. See vol. 154, pg. 4437, 2013) [J].
Aoki, Naohito ;
Jin-No, Shinji ;
Nakagawa, Yoshimi ;
Asai, Noriyuki ;
Arakawa, Erina ;
Tamura, Noriko ;
Tamura, Tomohiro ;
Matsuda, Tsukasa .
ENDOCRINOLOGY, 2007, 148 (08) :3850-3862
[10]   Heat shock protein-containing exosomes in mid-trimester amniotic fluids [J].
Asea, Alexzander ;
Jean-Pierre, Claudel ;
Kaur, Punit ;
Rao, Preethi ;
Linhares, Iara M. ;
Skupski, Daniel ;
Witkin, Steven S. .
JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2008, 79 (01) :12-17