Identification of the envelope V3 loop as a determinant of a CD4-negative neuronal cell tropism for HIV-1

被引:43
作者
Trujillo, JR [1 ]
Wang, WK [1 ]
Lee, TH [1 ]
Essex, M [1 ]
机构
[1] HARVARD UNIV,SCH PUBL HLTH,DEPT CANC BIOL,BOSTON,MA 02115
关键词
D O I
10.1006/viro.1996.0158
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Some neuronal-derived CD4-negative cells are susceptible to infection with human immunodeficiency virus type 1 (HIV-1). Galactosyl ceramide is an alternate receptor for HIV-1 that appears to bind in vitro to the C2, vs, V4, and V5 regions of gp 120. Amino acid variation in the vs loop of HIV-1 affects cellular tropism in CD4-positive cells, but its effect on CD4-negative cells has not been fully analyzed. Here, we describe the effect of amino acid changes in vs on the HIV-1 infection of a CD4-negative neuronal cell line, SK-N-MC. The sequence of the V3 domain was found to dramatically alter virus infectivity. Furthermore, a gp120 V3 loop neutralizing monoclonal antibody blocked HIV-1 infection on SK-N-MC cells. This data suggests that vs may also serve as a primary viral determinant for infectivity of CD4-negative cells. (C) 1996 Academic Press, Inc.
引用
收藏
页码:613 / 617
页数:5
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