Fusion of monocytes and macrophages with HIV-1 correlates with biochemical properties of CXCR4 and CCR5
Cheryl K. Lapham1, Marina B. Zaitseva1, 2, Shirley Lee1, 2, Tatiana Romanstseva1
& Hana Golding1
1
Division of Viral Products, Center for Biologics Evaluation and Research
(CBER), Food and Drug Administration, HFM-454, 8800 Rockville Pike, Bethesda, Maryland 20892, USA
2
M.B.Z. and S.L. contributed equally to this study
Human macrophages can be infected more efficiently by M-tropic than by T-tropic HIV-1 strains, despite surface expression of both CXCR4 and CCR5 co-receptors. Western blot analyses of total cell extracts and surface proteins from multiple sets of monocytes and macrophages demonstrated substantial differences between CXCR4 molecules. CXCR4 was mainly a monomer in monocytes, but was mainly a species of higher molecular weight (90 kDa) on the surface of macrophages. CCR5 was monomeric in both cell types. A constitutive association between CD4 and the co-receptors was seen in monocytes and macrophages. However, CD4 co-precipitated with CCR5 and CXCR4 monomers, but not with the high-molecular-weight forms of CXCR4, indicating that the high-molecular-weight CXCR4 species in macrophages are not available for association with CD4, which may contribute to the inefficient entry of T-tropic strains into mature macrophages.
