## Abstract Surface glycoproteins of normal human B lymphocytes, B blasts and various types of lymphoid cell lines were labelled by the galactose oxidase‐tritiated sodium borohydride method. The labelled glycoproteins were separated by polyacryUmide slab gel electrophoresis in the presence of sodiu
Spontaneous outgrowth of epstein-barr virus-positive B-cell lines from circulating human B cells of different buoyant densities
✍ Scribed by Q. Y. Yao; H. Czarnecka; A. B. Rickinson
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- French
- Weight
- 543 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Epstein‐Barr virus (EBV) has potent cell‐growth‐transforming activity for human B lymphocytes in vitro, yet appears to persist in the circulating B‐cell pool of virus carriers in vivo as a largely asymptomatic (i.e., non‐growth‐transforming) infection. The true nature of this infection, and the identity of the cells involved, remain to be determined. Studies of Lewin et al. (1987) have suggested (i) that the frequency of virus‐infected cells in the circulating B‐cell pool differs in different buoyant density fractions, being most abundant in the low‐density population, and (ii) that rare virus‐infected cells with the capacity for direct in vitro outgrowth to EBV‐transformed cell lines are segregated within the high‐density population. We have repeated this work using B‐cell fractions from a much larger panel of asymptomatic virus carriers and find (i) that the incidence of virus‐infected B cells Is not significantly different between high‐and low‐density fractions, and (ii) that virus‐infected cells from both fractions give rise to EBV‐transformed cell lines in culture predominantly through a 2‐step mechanism of virus replication and secondary infection rather than by direct outgrowth.
📜 SIMILAR VOLUMES
## Abstract Variation of Epstein‐Barr virus (EBV) in respect to its effect on the properties of transformed cells was probed. Human umbilical cord leukocytes from six different individuals were transformed in vitro by either B95‐8 (B) or QIMR‐WIL (Q) strains of EBV and subsequently 12 lymphoblastoi