CELL-TO-CELL CONTACT VIA MEASLES-VIRUS HEMAGGLUTININ-CD46 INTERACTIONTRIGGERS CD46 DOWN-REGULATION

Citation
S. Krantic et al., CELL-TO-CELL CONTACT VIA MEASLES-VIRUS HEMAGGLUTININ-CD46 INTERACTIONTRIGGERS CD46 DOWN-REGULATION, Journal of General Virology, 76, 1995, pp. 2793-2800
Citations number
29
Categorie Soggetti
Virology,"Biothechnology & Applied Migrobiology
Journal title
ISSN journal
00221317
Volume
76
Year of publication
1995
Part
11
Pages
2793 - 2800
Database
ISI
SICI code
0022-1317(1995)76:<2793:CCVMHI>2.0.ZU;2-Y
Abstract
CD46 downregulation by measles virus (MV) occurs after expression of v irus haemagglutinin (H) protein on the surface of the infected cell an d is a consequence of CD46-H interaction on the cell membrane. To asse ss whether CD46 downregulation also occurs after CD46-H interaction wh en these two molecules are expressed on distinct cells, we used human T cell line Jurkat (expressing CD46) and transfected murine fibroblast line L stably expressing MV-H protein (L.H). FAGS analysis shows that cell-to-cell contact of 1 h at 37 degrees C triggers a reduction of C D46 cell surface labelling as detected by MCI20.6, GB24 and J4-48 mono clonal antibodies. This reduction is similar to that observed after MV infection or after infection with recombinant vaccinia virus encoding MV-H protein. By contrast, MV-H protein was downregulated only when C D46-H interaction occurred on the same cell membrane. CD46 downregulat ion is specific for CD46-H interaction because it was not observed aft er coincubation of Jurkat cells with either L cells expressing MV nucl eoprotein (L.NP) or L cells. Moreover, this downregulation could be bl ocked by either anti-CD46 or anti-H antibodies. The II-mediated CD46 d ownregulation is reversible and restricted to CD46 since expression of other surface markers (CD3, CD14, CD47 and CD63) is unaffected. It is apparently not mediated in a protein kinase (PK) A- or PKC-dependent manner. Altogether, our results provide an unequivocal demonstration t hat interaction between the extracellular domains of CD46 and MV-H is sufficient to trigger CD46 downregulation.