Sendai virus replication in Friend erythroleukemia cells. I. Acutely and persistently infected cells become resistant to virus-induced lysis

1986 ◽  
Vol 4 (2) ◽  
pp. 117-132
Author(s):  
Arrigo Benedetto ◽  
Carla Amici ◽  
Stefania Zaniratti ◽  
Giuliano Elia ◽  
Maria Pia Camporiondo
Virology ◽  
1990 ◽  
Vol 177 (1) ◽  
pp. 131-140 ◽  
Author(s):  
H.E. Homann ◽  
P.H. Hofschneider ◽  
W.J. Neubert

1982 ◽  
Vol 2 (12) ◽  
pp. 1472-1480 ◽  
Author(s):  
Miriam Friedman-Einat Michel Revel ◽  
Adi Kimchi

A gradual increase in the level of 2′,5′-oligoadenylate synthetase takes place in Friend erythroleukemia cells after a shiftdown in the rate of cell growth. The increase is about 5-fold after entry of cells into the stationary phase of growth, but much higher (25-fold) when reduction in growth accompanies cell differentiation. In the latter case, the enzyme increase is similar to that which can be induced in these cells by exogenous interferon (IFN). The increase in 2′,5′-oligoadenylate synthetase was shown to be due to a spontaneous secretion of IFN by the cells themselves: it is completely abolished if antiserum to murine type I IFN is added to the culture medium. In attempts to isolate some of this spontaneously secreted IFN, we show that it is stable at pH 2, not neutralized by antiserum to type II IFN, and that it also differs from the known IFN species induced by Sendai virus in Friend cells. The major component of this spontaneously secreted IFN is 20,000Mrand differs from the corresponding virus-induced 20,000-MrIFN by its lower affinity for antiserum to type I IFN and its antigenic characterization as β-murine IFN. The major component of the spontaneous IFN also exhibits a higher ratio of antigrowth to antiviral activity than the Sendai-induced IFNs. We suggest that Friend cells produce this specific type of IFN for the regulation of their growth and differentiation.


1986 ◽  
Vol 5 (2-3) ◽  
pp. 221-234 ◽  
Author(s):  
Kristina M. Obom ◽  
Steven W. Popple ◽  
J.Gilbert Holland ◽  
Beatriz G.-T. Pogo ◽  
Charlotte Friend

2004 ◽  
Vol 78 (21) ◽  
pp. 11939-11951 ◽  
Author(s):  
Morihiro Ito ◽  
Taijiro Takeuchi ◽  
Machiko Nishio ◽  
Mitsuo Kawano ◽  
Hiroshi Komada ◽  
...  

ABSTRACT We obtained 157 cloned cell lines persistently infected with Sendai virus; these cell lines were generated independently of each other. Infectious viruses could be isolated from 123 of these cloned cell lines by inoculation of culture fluids or infected cells into embryonated eggs. The majority of the viruses carried by cells persistently infected with viruses showed high cytotoxicity and did not have the ability to establish persistent infection. The association of carried virus with cells became stronger and virus isolation correspondingly became more difficult as cells persistently infected with virus were subcultured. Viruses derived from virus-infected cells eventually acquired the ability to establish persistent infection, although the ways in which the viruses acquired this ability varied. The viruses also acquired temperature sensitivity as persistently infected cells were subcultured. First, the hemagglutinin-neuraminidase and M proteins acquired temperature sensitivity, and then the polymerase(s) did so. The M proteins were localized in the nuclei of cells infected with cloned viruses that had the ability to establish persistent infection. Cells infected with viruses capable of establishing persistent infection showed no or slight staining by terminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling. Specific amino acid substitutions accumulated in the M protein and the L protein as virus-infected cells were subcultured. This study shows that there is an unstable dynamic phase at an early stage of the establishment of persistent Sendai virus infection (steady state), and then viruses capable of establishing persistent infection are selected.


1998 ◽  
Vol 143 (10) ◽  
pp. 2039-2044 ◽  
Author(s):  
T. Mizutani ◽  
H. Inagaki ◽  
K. Araki ◽  
H. Kariwa ◽  
J. Arikawa ◽  
...  

1982 ◽  
Vol 2 (12) ◽  
pp. 1472-1480
Author(s):  
Miriam Friedman-Einat Michel Revel ◽  
Adi Kimchi

A gradual increase in the level of 2′,5′-oligoadenylate synthetase takes place in Friend erythroleukemia cells after a shiftdown in the rate of cell growth. The increase is about 5-fold after entry of cells into the stationary phase of growth, but much higher (25-fold) when reduction in growth accompanies cell differentiation. In the latter case, the enzyme increase is similar to that which can be induced in these cells by exogenous interferon (IFN). The increase in 2′,5′-oligoadenylate synthetase was shown to be due to a spontaneous secretion of IFN by the cells themselves: it is completely abolished if antiserum to murine type I IFN is added to the culture medium. In attempts to isolate some of this spontaneously secreted IFN, we show that it is stable at pH 2, not neutralized by antiserum to type II IFN, and that it also differs from the known IFN species induced by Sendai virus in Friend cells. The major component of this spontaneously secreted IFN is 20,000 M r and differs from the corresponding virus-induced 20,000- M r IFN by its lower affinity for antiserum to type I IFN and its antigenic characterization as β-murine IFN. The major component of the spontaneous IFN also exhibits a higher ratio of antigrowth to antiviral activity than the Sendai-induced IFNs. We suggest that Friend cells produce this specific type of IFN for the regulation of their growth and differentiation.


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