Document 3303 DOCN M94A3303 TI HIV-1 Vpu liberates Golgi-targeted HIV-1 env gp160 from CD4-dependent retention in the endoplasmic reticulum. DT 9412 AU Nishikawa M; Kimura T; Department of Microbiology, Kansai Medical University, Osaka,; Japan. SO Int Conf AIDS. 1994 Aug 7-12;10(1):107 (abstract no. PA0045). Unique Identifier : AIDSLINE ICA10/94369272 AB OBJECTIVE: The experiments were aimed to analyse the effects of HIV-1 Vpu on subcellular localization and processing of HIV-1 env gp160 that had been complexed and retained with CD4 molecules in the Endoplasmic reticulum (ER). METHODS: COS-1 cells were transfected to express HIV-1 env, vpu and rev, and CD4 genes. Analyses of oligosaccharides processing of gp160, and measurement of turn-over of CD4-gp160 complexes in the presence of and absence of Vpu were carried out on metabolically labelled COS-1 cells. In cycloheximide-treated cells a morphological chase was also performed to examine the effects of Vpu on the membrane traffic of gp160 coupled with CD4. RESULTS: When gp160 and Vpu were co-expressed from the singly spliced viral bicistronic mRNA, both molecules were independently targeted to the Golgi apparatus. Co-expression of CD4, however, resulted in the retention of gp160 in the ER but only observed in vpu-cells. Expression of Vpu selectively degraded CD4 and rendered the gp160 competent to translocate to the targeted Golgi complex. CONCLUSIONS: We concluded that Vpu prevents the formation of stable CD4-gp160 complexes in the ER, thereby, indirectly allows gp160 to accumulate in the Golgi apparatus where the protein is selectively retained to produce gp120-gp41. DE Animal Antigens, CD4/*METABOLISM Cell Line Endoplasmic Reticulum/METABOLISM/MICROBIOLOGY Gene Expression Gene Products, env/GENETICS/*METABOLISM Gene Products, vpu/GENETICS/*METABOLISM Genes, env Genes, rev Genes, vpu Golgi Apparatus/METABOLISM/MICROBIOLOGY Human HIV Envelope Protein gp120/METABOLISM HIV Envelope Protein gp41/METABOLISM HIV-1/GENETICS/*METABOLISM Protein Precursors/GENETICS/*METABOLISM Protein Processing, Post-Translational Transfection MEETING ABSTRACT SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).