Figure 6.
Figure 6. Primary human erythroid cells express both receptor and coreceptor for parvovirus B19 and internalize the virus. (A) Flow cytometric analyses of surface expression of P antigen (left), α5 (middle), and β1 (right) integrins in primary human erythroid progenitor cells. Control cells stained with secondary antibodies only are shown in black. Cell surface expression of P antigen, α5, and β1 integrins was analyzed by flow cytometry as described in “Materials and methods.” (B) Southern blot analysis of low Mr DNA isolated from uninfected (lane 1) and wt parvovirus B19-infected primary human erythroid progenitor cells (lane 2), which showed the presence of internalized single-stranded (ss) viral genomes. Inhibitory β1 integrin antibodies (lane 3) and parvovirus B19 anti-VP2 antibodies (lane 5) abrogated viral entry, whereas cross-linking of β1 integrin-inhibitory antibodies with secondary antibodies (JB1a+sec. Ab) had no significant effect (lane 4).

Primary human erythroid cells express both receptor and coreceptor for parvovirus B19 and internalize the virus. (A) Flow cytometric analyses of surface expression of P antigen (left), α5 (middle), and β1 (right) integrins in primary human erythroid progenitor cells. Control cells stained with secondary antibodies only are shown in black. Cell surface expression of P antigen, α5, and β1 integrins was analyzed by flow cytometry as described in “Materials and methods.” (B) Southern blot analysis of low Mr DNA isolated from uninfected (lane 1) and wt parvovirus B19-infected primary human erythroid progenitor cells (lane 2), which showed the presence of internalized single-stranded (ss) viral genomes. Inhibitory β1 integrin antibodies (lane 3) and parvovirus B19 anti-VP2 antibodies (lane 5) abrogated viral entry, whereas cross-linking of β1 integrin-inhibitory antibodies with secondary antibodies (JB1a+sec. Ab) had no significant effect (lane 4).

Close Modal

or Create an Account

Close Modal
Close Modal