- About Us
- Clinical Trials
- News Publications
- Business Development
December 5, 2005
Source: FEBS Lett 2005;579: 6549-58.
Authors: Evžen Bouřa, D. Liebl, Radek Špíšek, Jan Frič, M. Marek, J. Stokrová, Vladimír Holán, Jitka Forstová
A vector for preparation of mouse polyomavirus capsid-like particles for transfer of foreign peptides or proteins into cells was constructed. Model pseudocapsids carrying EGFP fused with the C-terminal part of the VP3 minor protein (EGFP-VLPs) have been prepared and analysed for their ability to be internalised and processed by mouse cells and to activate mouse and human dendritic cells (DC) in vitro. EGFP-VLPs entered mouse epithelial cells, fibroblasts and human and mouse DC efficiently and were processed by both, lysosomes and proteasomes. Surprisingly, they did not induce upregulation of DC co-stimulation molecules or maturation markers in vitro; however, they did induce interleukin 12 secretion.