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10.1097/00042560-199609000-00003

http://scihub22266oqcxt.onion/10.1097/00042560-199609000-00003
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8797681!ä!8797681

suck abstract from ncbi


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pmid8797681      J+Acquir+Immune+Defic+Syndr+Hum+Retrovirol 1996 ; 13 (1): 18-22
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  • Impairment of phagosome-lysosome fusion in HIV-1-infected macrophages #MMPMID8797681
  • Moorjani H; Craddock BP; Morrison SA; Steigbigel RT
  • J Acquir Immune Defic Syndr Hum Retrovirol 1996[Sep]; 13 (1): 18-22 PMID8797681show ga
  • Phagosome-lysosome fusion is critical for intracellular killing of most organisms and is inhibited by some viruses, notably influenza. We explored the effects of infection in vitro with HIV-1 (IIIB or Ada-M) on phagosome-lysosome fusion in blood monocyte-derived macrophages. After 8 days of infection, fusion was assessed from the fluorescence change occurring up to 2 h after labeling the lysosome compartment with acridine orange and loading of phagosomes with opsonized yeast. Compared with mock-infected control macrophages, the proportion of cells showing fusion after infection was reduced from a mean of 70% to a mean of 47% (p = 0.0001). Inhibition was seen with heat-killed HIV-1 IIIB but not virus-free filtrate. It was mimicked by recombinant gp 120 and blocked by soluble CD4 or antibody to CD4 but not by a neutralizing antibody to the V3 loop of gp 120. The inhibitory effect was seen 8 days after the original, transient exposure to gp 120. These results suggest that a lasting abnormality of phagosome-lysosome fusion results from interaction between gp 120 and CD4, contributing, perhaps, to the increased susceptibility to opportunistic infections of people infected with HIV.
  • |*HIV-1[MESH]
  • |CD4 Antigens/immunology/metabolism[MESH]
  • |Cells, Cultured[MESH]
  • |HIV Envelope Protein gp120/immunology/physiology[MESH]
  • |HIV Infections/*virology[MESH]
  • |Humans[MESH]
  • |Macrophages/*physiology/*virology[MESH]
  • |Microscopy, Fluorescence[MESH]
  • |Phagocytosis/*physiology[MESH]


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