Detection of receptors for hepatitis B virus on cells of extrahepatic origin

• Published in: Virology (New York, N.Y.) Vol. 176; no. 2; pp. 448 - 457
• Main Authors: Neurath, A.R., Strick, N., Sproul, P., Ralph, H.E., Valinsky, J.
• Format: Journal Article
• Language: English
• Published: San Diego, CA Elsevier Inc 01.06.1990; Elsevier
• Subjects: Amino Acid Sequence; B-Lymphocytes - metabolism; B-Lymphocytes - microbiology; Biological and medical sciences; Blotting, Western; Carcinoma, Hepatocellular; Cell Line; Chromatography, Affinity; Fundamental and applied biological sciences. Psychology; Hepatitis B Surface Antigens - metabolism; Hepatitis B virus - metabolism; Humans; Liver - metabolism; Liver - microbiology; Liver Neoplasms; Microbiology; Protein Precursors - metabolism; Receptors, Virus - analysis; Replicative cycle, interference, host-virus relations, pathogenicity, miscellaneous strains; Tumor Cells, Cultured; Viral Envelope Proteins - metabolism; Virology; Virus; Human; Binding; Proteins; Membrane receptor; Binding capacity; Cell line; Hepadnaviridae; Hepatitis B virus; Precursor; Cell surface
• ISSN: 0042-6822; 1096-0341
• DOI: 10.1016/0042-6822(90)90014-I

Receptors for hepatitis B virus (HBV; subtype adw) were identified on the surface of human hepatoma HepG2 cells in earlier studies. The cell receptor binding site on HBV was assigned to the preS(21–47) region of the preS1 sequence of the envelope protein. Studies presented here show that (1) amino acid residue replacements within the preS(21–47) sequence distinguishing HBV subtypes adw and ayw, preserve the binding capacity of the HBV env protein for HepG2 cell receptors; (2) the inhibition of binding between HepG2 cells and preS1-specific ligands by antibodies is effective only if the subtype specificity of anti-preS1-specific antibodies and of the preS1-specific ligands are matched; (3) receptors for HBV were present on the surface of human cells of nonhepatic origin, including peripheral blood B-lymphocytes, some hematopoietic cell lines of the B-cell lineage, neuroblastoma, amnion, and embryonic carcinoma cell lines. Receptors for HBV on these cells appeared similar to the receptor on HepG2 cells by the following criteria: (a) recognition by antibodies raised against the receptor on HepG2 cells; (b) inhibitory activity of lysates prepared from these cells on the interaction between HepG2 cells and preS1-specific ligands; and (c) the inhibitory effect of lysates from HepG2 cells on the reaction of these cells with HBsAg- and preS(21–47)-cellulose. The presence of receptors for HBV on some cells of extrahepatic origin is in accordance with earlier observations indicating that hepadnaviruses are not strictly hepatotropic.