Overview of extracellular microvesicles in drug metabolism

被引:38
作者
Conde-Vancells, Javier [1 ]
Gonzalez, Esperanza [1 ]
Lu, Shelly C. [2 ]
Mato, Jose M. [1 ]
Falcon-Perez, Juan M. [1 ]
机构
[1] CIBERehd, CICbioGUNE, Metab Unit, Bizkaia 48160, Spain
[2] Univ So Calif, Keck Sch Med, Div Gastrointestinal & Liver Dis, Los Angeles, CA 90033 USA
关键词
CELL-DERIVED EXOSOMES; HUMAN-SERUM-ALBUMIN; PROTEIN-PROTEIN INTERACTIONS; CYTOCHROMES P450; PROTEOMIC ANALYSIS; UDP-GLUCURONOSYLTRANSFERASES; CIRCULATING MICROPARTICLES; RETICULOCYTE MATURATION; MULTIVESICULAR BODIES; ENDOTHELIAL-CELLS;
D O I
10.1517/17425251003614766
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Areas covered in this review: A systematic bibliographic search focused on two related aspects: i) xenobiotic-metabolizing enzymes that have been detected in microvesicles (MVs); and ii) MVs that are in the blood stream or secreted by cell types with clear interactions with this fluid. What the reader will gain: A discussion of these hepatocyte-secreted vesicles along with other MVs as enzymatic carriers in the context of extrahepatic drug-metabolizing systems. Take home message: The contribution of many tissues including the liver to the MV plasma population is supported by several reports. On the other hand, many enzymes involved in the metabolism of drugs have been detected in MVs. Together, these observations support a role of hepatic-MVs in spreading the liver metabolizing activities through the body contributing in this manner to extrahepatic drug metabolism systems what could be relevant for body homeostasis and pharmaceutical interests.
引用
收藏
页码:543 / 554
页数:12
相关论文
共 101 条
[1]
Intercellular transfer of the oncogenic receptor EGFrvIII by microvesicles derived from tumour cells [J].
Al-Nedawi, Khalid ;
Meehan, Brian ;
Micallef, Johann ;
Lhotak, Vladimir ;
May, Linda ;
Guha, Abhijit ;
Rak, Janusz .
NATURE CELL BIOLOGY, 2008, 10 (05) :619-U24
[2]
Serum-derived exosomes from antigen-fed mice prevent allergic sensitization in a model of allergic asthma [J].
Almqvist, Nina ;
Lonnqvist, Anna ;
Hultkrantz, Susanne ;
Rask, Carola ;
Telemo, Esbjorn .
IMMUNOLOGY, 2008, 125 (01) :21-27
[3]
Cytochromes P450 and metabolism of xenobiotics [J].
Anzenbacher, P ;
Anzenbacherová, E .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2001, 58 (5-6) :737-747
[4]
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
[5]
Tumour-derived microvesicles carry several surface determinants and mRNA of tumour cells and transfer some of these determinants to monocytes [J].
Baj-Krzyworzeka, M ;
Szatanek, R ;
Weglarczyk, K ;
Baran, J ;
Urbanowicz, B ;
Branski, P ;
Ratajczak, MZ ;
Zembala, M .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2006, 55 (07) :808-818
[6]
Proteome of endothelial cell-derived procoagulant microparticles [J].
Banfi, C ;
Brioschi, M ;
Wait, R ;
Begum, S ;
Gianazza, E ;
Pirillo, A ;
Mussoni, L ;
Tremoli, E .
PROTEOMICS, 2005, 5 (17) :4443-4455
[7]
THE ALDO-KETO REDUCTASE SUPERFAMILY AND ITS ROLE IN DRUG METABOLISM AND DETOXIFICATION [J].
Barski, Oleg A. ;
Tipparaju, Srinivas M. ;
Bhatnagar, Aruni .
DRUG METABOLISM REVIEWS, 2008, 40 (04) :553-624
[8]
Basta S J, 1992, J Clin Anesth, V4, P153, DOI 10.1016/0952-8180(92)90034-X
[9]
DRUG-METABOLIZING-ENZYMES RELATED TO LABORATORY MEDICINE - CYTOCHROMES P-450 AND UDP-GLUCURONOSYLTRANSFERASES [J].
BATT, AM ;
MAGDALOU, J ;
VINCENTVIRY, M ;
OUZZINE, M ;
FOURNELGIGLEUX, S ;
GALTEAU, MM ;
SIEST, G .
CLINICA CHIMICA ACTA, 1994, 226 (02) :171-190
[10]
Membrane microparticles mediate transfer of P-glycoprotein to drug sensitive cancer cells [J].
Bebawy, M. ;
Combes, V. ;
Lee, E. ;
Jaiswal, R. ;
Gong, J. ;
Bonhoure, A. ;
Grau, G. E. R. .
LEUKEMIA, 2009, 23 (09) :1643-1649