Key result
Treatment of measles virus-infected 448-PI-Vero cells with 5 microM cyclosporin A enhanced cell fusion and increased the expression of measles virus antigen on the cell surface.
Why the study?
Does Cyclosporin A enhance cell fusion in monkey kidney cells persistently infected with measles virus?
Does Cyclosporin A enhance cell fusion in monkey kidney cells persistently infected with measles virus?
Cyclosporin A enhances cell fusion in measles virus-infected monkey kidney cells, likely by affecting the transport and accumulation of viral glycoproteins.
Answers are grounded in this paper and cite their sources.
CsA may modulate measles glycoprotein trafficking in vitro; leaves open in vivo relevance or therapeutic implications.
The authors studied the effects of immunosuppressive peptide cyclosporin A (CsA) on cell fusion efficiency in cells persistently infected with measles virus (448-PI-Vero cells). Treatment of 448-PI-Vero cells with 5 microM CsA enhanced the infusion. In addition, the expression of measles virus antigen on cell surface was increased by treatment with CsA. The addition of phenothiazine, an anti-calmodulin drug, enhanced the fusion of 448-PI-Vero cells in the presence of CsA, although treatment with phenothiazine alone did not affect polykaryocyte formation. The enhancement of fusion efficiency in 448-PI-Vero cells by CsA was suppressed by oligopeptide Z-D-Phe-Phe-Gly, a synthetic oligopeptide that inhibits fusion induced by measles virus. Since the cell content of major virus-specific polypeptides, such as hemagglutinin, nucleoprotein or matrix protein is the same as in untreated controls, this fusion enhancement may be related to transport and accumulation of measles virus glycoproteins.
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Watari et al. (2001) studied Measles virus persistent infection (in vitro). Cyclosporin A (CsA) vs. Untreated controls was evaluated on Cell fusion efficiency and expression of measles virus antigen on cell surface. Treatment of measles virus-infected 448-PI-Vero cells with 5 microM cyclosporin A enhanced cell fusion and increased the expression of measles virus antigen on the cell surface.
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