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Human immunodeficiency virus type 1 envelope glycoprotein gp120-mediated killing of human haematopoietic progenitors (CD34+ cells)
- Source :
- Journal of General Virology. 73:417-421
- Publication Year :
- 1992
- Publisher :
- Microbiology Society, 1992.
-
Abstract
- The effects of human immunodeficiency virus type 1 (HIV-1) and recombinant envelope glycoprotein gp120 on the in vitro growth of enriched human haematopoietic progenitors (CD34+ cells) have been investigated. A 2 h exposure to HIV-1 resulted in a progressive and significant reduction of viable CD34+ cell number in liquid cultures and of granulocyte-macrophage, erythroid and megakaryocytic progenitors in semisolid cultures. In virus-treated CD34+ cells, no signs of active virus replication were observed and the possibility of latent infection was excluded by quantitative polymerase chain reaction. Recombinant HIV-1 envelope glycoprotein gp120 added to CD34+ cell cultures displayed a dose-dependent inhibitory activity on CD34+ cell viability. Neutralizing antibody against gp120 was able to block completely the inhibitory activity on CD34+ cells of either HIV-1 or recombinant gp120. These results demonstrate that HIV-1 envelope glycoprotein gp120 has a direct cytotoxic effect on CD34+ cells.
- Subjects :
- Cell Survival
viruses
Dose-Response Relationship, Immunologic
Gene Products, gag
Antigens, CD34
Bone Marrow Cells
Cell Separation
HIV Envelope Protein gp120
Polymerase Chain Reaction
Virus
Viral envelope
Antigens, CD
HLA-DQ Antigens
Virology
Humans
Cytotoxic T cell
Progenitor cell
Neutralizing antibody
Cells, Cultured
biology
Gene Products, env
virus diseases
Hematopoietic Stem Cells
Envelope glycoprotein GP120
Molecular biology
Recombinant Proteins
Haematopoiesis
Cell culture
DNA, Viral
HIV-1
biology.protein
Cell Division
Subjects
Details
- ISSN :
- 14652099 and 00221317
- Volume :
- 73
- Database :
- OpenAIRE
- Journal :
- Journal of General Virology
- Accession number :
- edsair.doi.dedup.....04fd9817e475d16ab7c7a401b7c1201c
- Full Text :
- https://doi.org/10.1099/0022-1317-73-2-417