Depletion of the surface CD4 molecule by the envelope protein of human immunodeficiency virus expressed in a human CD4 sup + monocytoid cell line
Journal Article
·
· Journal of Virology; (USA)
OSTI ID:7066393
- Kyushu Univ., Fukuoka (Japan)
- Univ. of Tokyo (Japan)
A CD4{sup +} human monocytoid cell line, U937, was transfected with a constructed plasmid which has the envelope gene of human immunodeficiency virus under the transcriptional control of the human metallothionein IIA promoter and was cloned thereafter. These cloned cell lines (EH and EL cells) expressed the viral gp160 in the cytoplasm. The expression of surface CD4 antigen examined by Leu3a and OKT4 monoclonal antibodies, however, disappeared completely in EH cells, which produce a larger amount of gp160, while diminishing only partly in EL cells, which produce a smaller amount of gp160. These results indicate that the level of expression of surface CD4 antigen correlates inversely with the amount of intracellular gp160. Moreover, immunoprecipitation studies using lysate from EH cells showed that OKT4 monoclonal antibody precipitated a significant number of CD4 molecules even after surface CD4 disappeared. However, Leu3a monoclonal antibody, which recognizes the binding site for envelope protein, could not precipitate any CD4 molecules in the same cell lysate. Taken together, these results suggested that CD4 molecules are still synthesized normally after the augmented production of gp160 in the cells but form a complex with the envelope protein in the cytoplasm and become unable to be transported to the cell surface, resulting in the observed depletion of surface CD4 antigen. This mechanism may explain the decrease or absence of surface CD4 antigens in human lymphocytes infected with human immunodeficiency virus.
- OSTI ID:
- 7066393
- Journal Information:
- Journal of Virology; (USA), Journal Name: Journal of Virology; (USA) Vol. 63:9; ISSN 0022-538X; ISSN JOVIA
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
550701* -- Microbiology-- Tracer Techniques
59 BASIC BIOLOGICAL SCIENCES
AIDS
AIDS VIRUS
ANIMALS
ANTIBODIES
ANTIGENS
AUTORADIOGRAPHY
BETA DECAY RADIOISOTOPES
BETA-MINUS DECAY RADIOISOTOPES
BIOLOGICAL MATERIALS
BLOOD
BLOOD CELLS
BODY FLUIDS
CELL CONSTITUENTS
CHEMICAL REACTIONS
CROSS-LINKING
DAYS LIVING RADIOISOTOPES
DISEASES
DNA HYBRIDIZATION
ELECTRON CAPTURE RADIOISOTOPES
GENE REGULATION
GENE REPRESSORS
HEMIC DISEASES
HYBRIDIZATION
IMMUNE SYSTEM DISEASES
INFECTIOUS DISEASES
INTERMEDIATE MASS NUCLEI
IODINE 125
IODINE ISOTOPES
ISOTOPES
LEUKOCYTES
LIGHT NUCLEI
MAMMALS
MAN
MATERIALS
MEMBRANE PROTEINS
MESSENGER-RNA
METALLOPROTEINS
METALLOTHIONEIN
MICROORGANISMS
MONOCLONAL ANTIBODIES
MONOCYTES
NUCLEI
NUCLEIC ACIDS
NUCLEOPROTEINS
ODD-EVEN NUCLEI
ODD-ODD NUCLEI
ORGANIC COMPOUNDS
PARASITES
PHOSPHORUS 32
PHOSPHORUS ISOTOPES
PLASMIDS
POLYMERIZATION
PRIMATES
PROTEINS
RADIOISOTOPES
RNA
TRANSCRIPTION
VERTEBRATES
VIRAL DISEASES
VIRUSES
59 BASIC BIOLOGICAL SCIENCES
AIDS
AIDS VIRUS
ANIMALS
ANTIBODIES
ANTIGENS
AUTORADIOGRAPHY
BETA DECAY RADIOISOTOPES
BETA-MINUS DECAY RADIOISOTOPES
BIOLOGICAL MATERIALS
BLOOD
BLOOD CELLS
BODY FLUIDS
CELL CONSTITUENTS
CHEMICAL REACTIONS
CROSS-LINKING
DAYS LIVING RADIOISOTOPES
DISEASES
DNA HYBRIDIZATION
ELECTRON CAPTURE RADIOISOTOPES
GENE REGULATION
GENE REPRESSORS
HEMIC DISEASES
HYBRIDIZATION
IMMUNE SYSTEM DISEASES
INFECTIOUS DISEASES
INTERMEDIATE MASS NUCLEI
IODINE 125
IODINE ISOTOPES
ISOTOPES
LEUKOCYTES
LIGHT NUCLEI
MAMMALS
MAN
MATERIALS
MEMBRANE PROTEINS
MESSENGER-RNA
METALLOPROTEINS
METALLOTHIONEIN
MICROORGANISMS
MONOCLONAL ANTIBODIES
MONOCYTES
NUCLEI
NUCLEIC ACIDS
NUCLEOPROTEINS
ODD-EVEN NUCLEI
ODD-ODD NUCLEI
ORGANIC COMPOUNDS
PARASITES
PHOSPHORUS 32
PHOSPHORUS ISOTOPES
PLASMIDS
POLYMERIZATION
PRIMATES
PROTEINS
RADIOISOTOPES
RNA
TRANSCRIPTION
VERTEBRATES
VIRAL DISEASES
VIRUSES