1-Cinnamoyl-3,11-dihydroxymeliacarpin delays glycoprotein transport restraining virus multiplication without cytotoxicity

被引:12
作者
Bueno, Carlos A. [1 ]
Alche, Laura E. [1 ]
Barquero, Andrea A. [1 ]
机构
[1] UBA, FCEN, Dept Quim Biol, Virol Lab, Buenos Aires, DF, Argentina
关键词
Antiviral; Medicinal plants; Golgi apparatus; Secretary pathway; Transferrin receptor; HIV-INFECTION; LOCALIZATION; ORIGIN;
D O I
10.1016/j.bbrc.2010.01.068
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The 1-cinnamoyl-3,11-dihydroxymeliacarpin (CDM), isolated from extracts of Melia azedarach L., displays antiviral and immunomodulating properties. CDM is the first reported tetranortriterpenoid responsible for the alkalinization of intracellular compartments affecting both, viral endocytic and exocytic pathways. Considering that viral glycoprotein synthesis is completely dependent upon cellular membrane trafficking, we questioned whether CDM might also interfere with the normal transport of cellular glycoprotems. This study demonstrates that CDM promoted a transient block in the transport of two cellular glycoproteins, the transferrin receptor (TfR) and TNF-alpha. Nevertheless, CDM did not affect the transferrin binding ability of TfR and did not impede the TNF-alpha secretion. On the other hand, CDM disturbed the intracellular localization of capsid, glycoprotein and tegument proteins simultaneously in the same HSV-1 infected cells. Besides, we show that concanamycin A and monensin provoke a permanent blockage of viral and cellular glycoproteins, in contrast to the delay observed after CDM treatment. Thus, the delay on glycoprotein transport caused by CDM would account for the strong inhibition on virus multiplication without interfering with the bioactivity of cellular glycoproteins. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:32 / 37
页数:6
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