Document 0615 DOCN M95A0615 TI The macrophage mannose receptor can mediate the uptake of Mycobacterium avium-intracellulare. American Pediatric Society 104th annual meeting and Society for Pediatric Research 63rd annual meeting; 1994 May 2-5; Seattle. DT 9510 AU Kruskal BA; Super M; Rogers R; Ezekowitz RA; Harvard Medical School, Children's Hospital, Div. of Infectious; Diseases, Boston, MA, USA. SO Pediatr AIDS HIV Infect. 1994 Oct;5(5):319 (unnumbered abstract). Unique Identifier : AIDSLINE AIDS/95330429 AB In patients with HIV and disseminated M. avium-intracellulare (MAI) infection, large numbers of MAI reside within macrophage phagosomes and survive there, resisting intrinsic macrophage antimycobacterial mechanisms. How MAI enter macrophages and survive has not been well elucidated thus far. Several macrophage cell-surface proteins have been shown to bind MAI, but none has yet been demonstrated to mediate uptake. Mycobacteria possess cell-membrane glycolipids rich in mannose, termed lipoarabinomannans, which suggested that the macrophage mannose receptor (MR), a phagocytic receptor, might be responsible for ingestion of MAI. We stably transfected HeLa cells with the cDNA for the human macrophage mannose receptor using the calcium phosphate method. Expressing cells were cloned twice. Stable HeLa transfectants expressing the MR were able to ingest MAI, as demonstrated by confocal fluorescence microscopy. Interestingly, non-transfected HeLa cells had a low level of intrinsic uptake activity. This observation demonstrates that the mannose receptor is able to mediate uptake of MAI, and that it may be important in the pathogenesis of MAI infection in AIDS. This experimental system will permit the comparison of different receptors for their ability to ingest MAI. DE AIDS-Related Opportunistic Infections/METABOLISM/*MICROBIOLOGY Child Hela Cells Human Macrophages/IMMUNOLOGY/METABOLISM/*MICROBIOLOGY Mycobacterium avium-intracellulare Infection/METABOLISM/ *MICROBIOLOGY Phagocytosis Receptors, Cell Surface/*METABOLISM Transfection MEETING ABSTRACT JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).