Human Primary Macrophages Derived In Vitro from Circulating Monocytes Comprise Adherent and Non-Adherent Subsets with Differential Expression of Siglec-1 and CD4 and Permissiveness to HIV-1 Infection

• Published in: Frontiers in immunology 2017-10, Vol.8, p.1352-1352
• Main Authors: Jobe, Ousman, Kim, Jiae, Tycksen, Eric, Onkar, Sayali, Michael, Nelson L, Alving, Carl R, Rao, Mangala
• Format: Article
• Language: English
• Subjects: CD4; human immunodeficiency virus type 1; Immunology; monocyte-derived macrophages; restriction factors; RNA-Seq; Siglec-1
• ISSN: 1664-3224; 1664-3224
• DOI: 10.3389/fimmu.2017.01352

Macrophages are a major target for human immunodeficiency virus type 1 (HIV-1) infection. However, macrophages are largely heterogeneous and may exhibit differences in permissiveness to HIV-1 infection. This study highlights the interplay of macrophage heterogeneity in HIV-1 pathogenesis. We show that monocyte-derived macrophages (MDMs) could be divided into two distinct subsets: CD14 Siglec-1 CD4 (non-adherent MDM) and CD14 Siglec-1 CD4 (adherent MDM). The CD14 Siglec-1 CD4 MDM subset represented the smaller proportion in the macrophage pool, and varied among different donors. Fractionation and subsequent exposure of the two MDM subsets to HIV-1 revealed opposite outcomes in terms of HIV-1 capture and infection. Although the CD14 Siglec-1 CD4 MDM captured significantly more HIV-1, infection was significantly higher in the CD14 Siglec-1 CD4 MDM subset. Thus, CD14 Siglec-1 CD4 MDM were less permissive to infection. Depletion of CD14 Siglec-1 CD4 MDM or a decrease in their percentage, resulted in increased infection of MDM, suggestive of a capacity of these cells to capture and sequester HIV-1 in an environment that hinders its infectivity. Increased expression of innate restriction factors and cytokine genes were observed in the non-adherent CD14 Siglec-1 CD4 MDM, both before and after HIV-1 infection, compared to the adherent CD14 Siglec-1 CD4 MDM. We speculate that the differential expression of gene expression profiles in the two macrophage subsets may provide an explanation for the differences observed in HIV-1 infectivity.