PMID- 9525591 OWN - NLM STAT- MEDLINE DCOM- 19980417 LR - 20200724 IS - 0022-538X (Print) IS - 1098-5514 (Electronic) IS - 0022-538X (Linking) VI - 72 IP - 4 DP - 1998 Apr TI - Immature dendritic cells selectively replicate macrophagetropic (M-tropic) human immunodeficiency virus type 1, while mature cells efficiently transmit both M- and T-tropic virus to T cells. PG - 2733-7 AB - Dendritic cells (DCs) can develop from CD14+ peripheral blood monocytes cultured in granulocyte-macrophage colony-stimulating factor (GM-CSF) and interleukin 4 (IL-4). By 6 days in culture, the cells have the characteristics of immature DCs and can be further induced to mature by inflammatory stimuli or by monocyte-conditioned medium. After infection with macrophagetropic (M-tropic) human immunodeficiency virus type 1 (HIV-1), monocytes and mature DCs show a block in reverse transcription and only form early transcripts that can be amplified with primers for the R/U5 region. In contrast, immature DCs cultured for 6 or 11 days in GM-CSF and IL-4 complete reverse transcription and show a strong signal when LTR/gag primers are used. Blood monocytes and mature DCs do not replicate HIV-1, whereas immature DCs can be productively infected, but only with M-tropic HIV-1. The virus produced by immature DCs readily infects activated T cells. Although mature DCs do not produce virus, these cells transmit both M- and T-tropic virus to T cells. In the cocultures, both DCs and T cells must express functional chemokine coreceptors for viral replication to occur. Therefore, the developmental stage of DCs can influence the interaction of these cells with HIV-1 and influence the extent to which M-tropic and T-tropic virus can replicate. FAU - Granelli-Piperno, A AU - Granelli-Piperno A AD - Laboratory of Cellular Physiology and Immunology, Rockefeller University, New York, New York 10021, USA. piperno@rockvax.rockefeller.edu FAU - Delgado, E AU - Delgado E FAU - Finkel, V AU - Finkel V FAU - Paxton, W AU - Paxton W FAU - Steinman, R M AU - Steinman RM LA - eng GR - N01AI40045/AI/NIAID NIH HHS/United States GR - R01 AI040874/AI/NIAID NIH HHS/United States GR - AI 40874/AI/NIAID NIH HHS/United States PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Research Support, U.S. Gov't, P.H.S. PL - United States TA - J Virol JT - Journal of virology JID - 0113724 RN - 0 (Receptors, CCR5) SB - IM MH - Cell Communication MH - Cells, Cultured MH - Dendritic Cells/physiology/*virology MH - HIV-1/*physiology MH - Humans MH - Macrophages/*virology MH - Receptors, CCR5/metabolism MH - T-Lymphocytes/*virology MH - *Virus Replication PMC - PMC109716 EDAT- 1998/04/03 00:00 MHDA- 1998/04/03 00:01 PMCR- 1998/04/01 CRDT- 1998/04/03 00:00 PHST- 1998/04/03 00:00 [pubmed] PHST- 1998/04/03 00:01 [medline] PHST- 1998/04/03 00:00 [entrez] PHST- 1998/04/01 00:00 [pmc-release] AID - 1215 [pii] AID - 10.1128/JVI.72.4.2733-2737.1998 [doi] PST - ppublish SO - J Virol. 1998 Apr;72(4):2733-7. doi: 10.1128/JVI.72.4.2733-2737.1998.