N-terminal Slit2 inhibits HIV-1 replication by regulating the actin cytoskeleton.
N-terminal Slit2 inhibits HIV-1 replication by regulating the actin cytoskeleton.
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DOI：
10.1186/1742-4690-10-2
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发表时间：
2013-01-07
期刊：
影响因子：
3.3
通讯作者：
Ganju RK
中科院分区：
文献类型：
--
作者：
Anand AR;Zhao H;Nagaraja T;Robinson LA;Ganju RK
Slit2 is a ~ 200 kDa secreted glycoprotein that has been recently shown to regulate immune functions. However, not much is known about its role in HIV (human immunodeficiency virus)-1 pathogenesis. In the present study, we have shown that the N-terminal fragment of Slit2 (Slit2N) (~120 kDa) inhibits replication of both CXCR4 and CCR5-tropic HIV-1 viruses in T-cell lines and peripheral blood T-cells. Furthermore, we demonstrated inhibition of HIV-1 infection in resting CD4+ T-cells. In addition, we showed that Slit2N blocks cell-to-cell transmission of HIV-1. We have shown that Slit2N inhibits HIV-1 infection by blocking viral entry into T-cells. We also ruled out Slit2N-mediated inhibition of various other steps in the life cycle including binding, integration and viral transcription. Elucidation of the molecular mechanism revealed that Slit2N mediates its functional effects by binding to Robo1 receptor. Furthermore, we found that Slit2N inhibited Gp120-induced Robo1-actin association suggesting that Slit2N may inhibit cytoskeletal rearrangements facilitating HIV-1 entry. Studies into the mechanism of inhibition of HIV-1 revealed that Slit2N abrogated HIV-1 envelope-induced actin cytoskeletal dynamics in both T-cell lines and primary T-cells. We further showed that Slit2N specifically attenuated the HIV-1 envelope-induced signaling pathway consisting of Rac1, LIMK and cofilin that regulates actin polymerization. Taken together, our results show that Slit2N inhibits HIV-1 replication through novel mechanisms involving modulation of cytoskeletal dynamics. Our study, thus, provides insights into the role of Slit2N in HIV-1 infection and underscores its potential in limiting viral replication in T-cells.
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DOI：
10.1007/978-1-59745-170-3_5
发表时间：
2009
期刊：
Methods in molecular biology (Clifton, N.J.)
影响因子：
--
作者：
Mbisa JL;Delviks-Frankenberry KA;Thomas JA;Gorelick RJ;Pathak VK
通讯作者：
Pathak VK
影响因子：
17.1
作者：
London NR;Zhu W;Bozza FA;Smith MC;Greif DM;Sorensen LK;Chen L;Kaminoh Y;Chan AC;Passi SF;Day CW;Barnard DL;Zimmerman GA;Krasnow MA;Li DY
通讯作者：
Li DY
影响因子：
21.3
作者：
Jimenez-Baranda, Sonia;Gomez-Mouton, Concepcion;Manes, Santos
通讯作者：
Manes, Santos
影响因子：
5.4
作者：
Canki, M;Thai, JNF;Volsky, DJ
通讯作者：
Volsky, DJ
影响因子：
4.4
作者：
Chen, B;Blair, DG;Yang, D
通讯作者：
Yang, D