N-terminal Slit2 inhibits HIV-1 replication by regulating the actin cytoskeleton

<p>Abstract</p> <p>Background</p> <p>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.</p> <p>Results</p>...

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Main Authors: Anand Appakkudal R, Zhao Helong, Nagaraja Tirumuru, Robinson Lisa A, Ganju Ramesh K
Format: Article
Language:English
Published: BMC 2013-01-01
Series:Retrovirology
Online Access:http://www.retrovirology.com/content/10/1/2
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author Anand Appakkudal R
Zhao Helong
Nagaraja Tirumuru
Robinson Lisa A
Ganju Ramesh K
author_facet Anand Appakkudal R
Zhao Helong
Nagaraja Tirumuru
Robinson Lisa A
Ganju Ramesh K
author_sort Anand Appakkudal R
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>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.</p> <p>Results</p> <p>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.</p> <p>Conclusions</p> <p>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.</p>
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spelling doaj.art-3d4b53a47a7d433aa4a5aacaf48140512022-12-22T01:36:32ZengBMCRetrovirology1742-46902013-01-01101210.1186/1742-4690-10-2N-terminal Slit2 inhibits HIV-1 replication by regulating the actin cytoskeletonAnand Appakkudal RZhao HelongNagaraja TirumuruRobinson Lisa AGanju Ramesh K<p>Abstract</p> <p>Background</p> <p>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.</p> <p>Results</p> <p>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.</p> <p>Conclusions</p> <p>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.</p>http://www.retrovirology.com/content/10/1/2
spellingShingle Anand Appakkudal R
Zhao Helong
Nagaraja Tirumuru
Robinson Lisa A
Ganju Ramesh K
N-terminal Slit2 inhibits HIV-1 replication by regulating the actin cytoskeleton
Retrovirology
title N-terminal Slit2 inhibits HIV-1 replication by regulating the actin cytoskeleton
title_full N-terminal Slit2 inhibits HIV-1 replication by regulating the actin cytoskeleton
title_fullStr N-terminal Slit2 inhibits HIV-1 replication by regulating the actin cytoskeleton
title_full_unstemmed N-terminal Slit2 inhibits HIV-1 replication by regulating the actin cytoskeleton
title_short N-terminal Slit2 inhibits HIV-1 replication by regulating the actin cytoskeleton
title_sort n terminal slit2 inhibits hiv 1 replication by regulating the actin cytoskeleton
url http://www.retrovirology.com/content/10/1/2
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AT robinsonlisaa nterminalslit2inhibitshiv1replicationbyregulatingtheactincytoskeleton
AT ganjurameshk nterminalslit2inhibitshiv1replicationbyregulatingtheactincytoskeleton