KINETICS OF HIV-INFECTION OF HUMAN PLACENTAL SYNCYTIOTROPHOBLAST CULTURES - AN ULTRASTRUCTURAL AND IMMUNOCYTOCHEMICAL STUDY

Citation
F. Fazely et al., KINETICS OF HIV-INFECTION OF HUMAN PLACENTAL SYNCYTIOTROPHOBLAST CULTURES - AN ULTRASTRUCTURAL AND IMMUNOCYTOCHEMICAL STUDY, AIDS research and human retroviruses, 11(9), 1995, pp. 1023-1030
Citations number
34
Categorie Soggetti
Immunology,"Infectious Diseases
ISSN journal
08892229
Volume
11
Issue
9
Year of publication
1995
Pages
1023 - 1030
Database
ISI
SICI code
0889-2229(1995)11:9<1023:KOHOHP>2.0.ZU;2-W
Abstract
We previously demonstrated that syncytiotrophoblast (ST) cells from te rm human placentas could be infected when cocultured with HIV-infected lymphocytic cells, Here, we have used fluorescence microscopy and tra nsmission electron microscopy to examine the kinetics of this infectio n process, Molt-4 clone 8 cells infected with HIV-1(Lai) or filtered s upernatant from these cultures were incubated with ST cells for differ ent times, In cell-associated infection, immunofluorescence microscopy revealed that some ST colonies were positive for HIV core proteins (p 24,p55) after 1 hr, The number of positive colonies and the intensity of the ST-associated fluorescence increased with time, Transmission el ectron microscopy showed viral particles with HIV morphology associate d with the ST cell surface at 1 hr, Immature virions with budding morp hology were observed at 2 hr, In cell-free infection, positive p24,p55 staining was first detected in a few ST colonies at 4 hr, The number of positive colonies increased with time, At 24 hr, the fluorescence p attern and intensity resembled that seen with cell-mediated infection at 4 hr, Transmission electron microscopy revealed an increasing numbe r of viral particles associated with the ST cell plasma membrane with respect to time, and budding virions first appeared at 8 hr, These res ults demonstrate that HIV infection of placental ST cells proceeds ver y rapidly in culture and that, furthermore, cell-associated infection of ST is much more efficient than the infection with cell-free virus.