| Full text | |
| Author(s): |
Amorim, Nathaly A.
[1]
;
da Silva, Eulalia M. L.
[1]
;
de Castro, Rodrigo O.
[1]
;
da Silva-Januario, Mara E.
[1]
;
Mendonca, Luiza M.
[2]
;
Bonifacino, Juan S.
[3]
;
da Costa, Luciana J.
[2]
;
daSilva, Luis L. P.
[1]
Total Authors: 8
|
| Affiliation: | [1] Univ Sao Paulo, Ribeirao Preto Sch Med, Dept Cell & Mol Biol, BR-14049900 Ribeirao Preto, SP - Brazil
[2] Univ Fed Rio de Janeiro, Inst Microbiol Paulo de Goes, Dept Virol, BR-21941590 Rio De Janeiro, RJ - Brazil
[3] Eunice Kennedy Shriver NICHD, Cell Biol & Metab Program, NIH, Bethesda, MD 20892 - USA
Total Affiliations: 3
|
| Document type: | Journal article |
| Source: | Journal of Biological Chemistry; v. 289, n. 40, p. 27744-27756, OCT 3 2014. |
| Web of Science Citations: | 18 |
| Abstract | |
Background: HIV-1 Nef targets the coreceptor CD4 to the multivesicular body (MVB) pathway for degradation via an unknown mechanism. Results: Nef interacts with Alix in late endosomes, and this is required for efficient lysosomal targeting of CD4. Conclusion: Nef utilizes Alix as an adaptor to target CD4 for lysosomal degradation. Significance: The study clarifies the mechanism by which Nef down-regulates expression of specific host-cell proteins. Nef is an accessory protein of human immunodeficiency viruses that promotes viral replication and progression to AIDS through interference with various host trafficking and signaling pathways. A key function of Nef is the down-regulation of the coreceptor CD4 from the surface of the host cells. Nef-induced CD4 down-regulation involves at least two independent steps as follows: acceleration of CD4 endocytosis by a clathrin/AP-2-dependent pathway and targeting of internalized CD4 to multivesicular bodies (MVBs) for eventual degradation in lysosomes. In a previous work, we found that CD4 targeting to the MVB pathway was independent of CD4 ubiquitination. Here, we report that this targeting depends on a direct interaction of Nef with Alix/AIP1, a protein associated with the endosomal sorting complexes required for transport (ESCRT) machinery that assists with cargo recruitment and intraluminal vesicle formation in MVBs. We show that Nef interacts with both the Bro1 and V domains of Alix. Depletion of Alix or overexpression of the Alix V domain impairs lysosomal degradation of CD4 induced by Nef. In contrast, the V domain overexpression does not prevent cell surface removal of CD4 by Nef or protein targeting to the canonical ubiquitination-dependent MVB pathway. We also show that the Nef-Alix interaction occurs in late endosomes that are enriched in internalized CD4. Together, our results indicate that Alix functions as an adaptor for the ESCRT-dependent, ubiquitin-independent targeting of CD4 to the MVB pathway induced by Nef. (AU) | |