Toxicity of derivatives from semicarbazide-sensitive amine oxidase-mediated deamination of methylamine against Toxoplasma gondii after infection of differentiated 3T3-L1 cells

被引:3
作者
Zhu, Sha [1 ]
Li, Qian-ru [1 ]
Du, Ying [1 ]
Yang, Xuan [1 ]
Fan, Jian-ming [3 ]
Dong, Zi-ming [2 ]
机构
[1] Zhengzhou Univ, Coll Basic Med Sci, Dept Microbiol & Immunol, Zhengzhou 450001, Henan, Peoples R China
[2] Zhengzhou Univ, Coll Basic Med Sci, Dept Pathophysiol, Zhengzhou 450001, Henan, Peoples R China
[3] Zhengzhou Univ, Coll Publ Hlth, Toxicol Lab, Zhengzhou 450001, Henan, Peoples R China
关键词
Cytotoxicity; Semicarbazide-sensitive aminoxidase; Methylamine; Toxoplasma gondii; SMOOTH-MUSCLE-CELLS; VASCULAR ENDOTHELIAL-CELLS; GLUCOSE-TRANSPORT; OXIDATIVE STRESS; HUMAN ADIPOCYTES; PLASMA-MEMBRANE; FORMALDEHYDE; APOPTOSIS; IDENTIFICATION; INSULIN;
D O I
10.1016/j.tiv.2009.12.014
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Adipose tissue plays an active role in normal metabolic homeostasis as well as in the development of human diseases such as atherosclerosis and diabetes. We report here antimicrobial activities of the metabolites from adipocytes. Specifically, semicarbazide-sensitive amine oxidase of differentiated 3T3-L1 cells was found to utilize methylamine for producing formaldehyde and hydrogen peroxide, accounting for the inhibition of infectivity of Toxoplasma gondii and its replication in these cells. This was demonstrated by the findings that semicarbazide-sensitive amine oxidase was extremely high in differentiated 3T3-L1 cells: and that the infection of these cells by T. gondii and its intracellular replication were decreased to 33% and 37% of the control, respectively, when methylamine was provided in micromolar concentrations as the substrate to the aminoxidase. Only one of the two reaction products expected was found inhibitory against T. gondii when added to the infected pre-adipocytes of 3T3-L1. Intracellular replication of this parasite was inhibited by formaldehyde in the range of 10-100 mu M and stimulated by hydrogen peroxide at 1-10 mu M. The finding indicates that T. gondii may be useful as a sensitive and convenient sentinel for screening agents toxic to eukaryotic cells. Published by Elsevier Ltd.
引用
收藏
页码:809 / 814
页数:6
相关论文
共 37 条
[1]   Modified LDLs induce proliferation-mediated death of human vascular endothelial cells through MAPK pathway [J].
Apostolov, Eugene O. ;
Basnakian, Alexei G. ;
Yin, Xiaoyan ;
Ok, Ercan ;
Shah, Sudhir V. .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2007, 292 (04) :H1836-H1846
[2]   Adipogenesis-related increase of semicarbazide-sensitive amine oxidase and monoamine oxidase in human adipocytes [J].
Bour, Sandy ;
Daviaud, Daniele ;
Gres, Sandra ;
Lefort, Corinne ;
Prevot, Danielle ;
Zorzano, Antonio ;
Wabitsch, Martin ;
Saulnier-Blache, Jean-Sebastien ;
Valet, Philippe ;
Carpene, Christian .
BIOCHIMIE, 2007, 89 (08) :916-925
[3]   The effect of cytokines on the replication of T-gondii within rat retinal vascular endothelial cells [J].
Brunton, CL ;
Wallace, GR ;
Graham, E ;
Stanford, MR .
JOURNAL OF NEUROIMMUNOLOGY, 2000, 102 (02) :182-188
[4]   The Toxoplasma gondii rhoptry protein ROP4 is secreted into the parasitophorous vacuole and becomes phosphorylated in infected cells [J].
Carey, KL ;
Jongco, AM ;
Kam, K ;
Ward, GE .
EUKARYOTIC CELL, 2004, 3 (05) :1320-1330
[5]   Dose response for formaldehyde-induced cytotoxicity in the human respiratory tract [J].
Conolly, RB ;
Kimbell, JS ;
Janszen, DB ;
Miller, FJ .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 2002, 35 (01) :32-43
[6]  
DEMELO EJT, 1992, CELL STRUCT FUNCT, V17, P311, DOI 10.1247/csf.17.311
[7]   Role of semicarbazide-sensitive amine oxidase on glucose transport and GLUT4 recruitment to the cell surface in adipose cells [J].
Enrique-Tarancón, G ;
Marti, L ;
Morin, N ;
Lizcano, JM ;
Unzeta, M ;
Sevilla, L ;
Camps, M ;
Palacín, M ;
Testar, X ;
Carpéné, C ;
Zorzano, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (14) :8025-8032
[8]   Semicarbazide-sensitive amine oxidase catalyzes endothelial cell-mediated low density lipoprotein oxidation [J].
Exner, M ;
Hermann, M ;
Hofbauer, R ;
Kapiotis, S ;
Quehenberger, P ;
Speiser, W ;
Held, I ;
Gmeiner, BMK .
CARDIOVASCULAR RESEARCH, 2001, 50 (03) :583-588
[9]  
FAN JY, 1983, J CELL SCI, V61, P219
[10]   Amine oxidase substrates mimic several of the insulin effects on adipocyte differentiation in 3T3 F442A cells [J].
Fontana, E ;
Boucher, J ;
Marti, L ;
Lizcano, JM ;
Testar, X ;
Zorzano, A ;
Carpéné, C .
BIOCHEMICAL JOURNAL, 2001, 356 (03) :769-777