Literature DB >> 7487492

Interaction of reconstituted Sendai viral envelopes with sperm cells: reconstituted Sendai virus envelope-induced fusion-mediated introduction of foreign material into bull sperm cells.

O Nussbaum1, A Loyter.   

Abstract

Reconstituted Sendai virus envelopes (RSVE), i.e. membrane vesicles bearing the viral envelope glycoproteins and phospholipids, are able to fuse with bull sperm cells. This was inferred from the increase in the degree of fluorescence dequenching (DQ) obtained following incubation of fluorescently labeled (R18 labeled) RSVE with bull sperm cells and from electron microscopy studies of RSVE-sperm interaction. Only a low degree of DQ was observed, under the same conditions, with non-fusogenic fluorescently labeled RSVE. This, and electron microscopy results, show that binding and membrane fusion events occur between RSVE and sperm cells. In addition, DQ was observed following incubation of RSVE that had been pre-loaded with the self-quenched fluorochrome Calcein, with bull sperm cells, indicating fusion-mediated injection of the dye from the RSVE space into the sperm cells.

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Year:  1995        PMID: 7487492     DOI: 10.1007/bf01322534

Source DB:  PubMed          Journal:  Arch Virol        ISSN: 0304-8608            Impact factor:   2.574


  15 in total

1.  Animal viruses are able to fuse with prokaryotic cells. Fusion between Sendai or influenza virions and Mycoplasma.

Authors:  V Citovsky; S Rottem; O Nussbaum; Y Laster; R Rott; A Loyter
Journal:  J Biol Chem       Date:  1988-01-05       Impact factor: 5.157

2.  Resistance to NK cell-mediated cytotoxicity (in K-562 cells) does not correlate with class I MHC antigen levels.

Authors:  Z Reiter; Y Reiter; Z Fishelson; M Shinitzky; A Kessler; A Loyter; O Nussbaum; M Rubinstein
Journal:  Immunobiology       Date:  1991-09       Impact factor: 3.144

3.  Use of reconstituted Sendai virus envelopes for fusion-mediated microinjection of double-stranded RNA: inhibition of protein synthesis in interferon-treated cells.

Authors:  G Arad; M Hershkovitz; A Panet; A Loyter
Journal:  Biochim Biophys Acta       Date:  1986-07-10

4.  Prevention of hemolysis by bivalent metal ions during virus-induced fusion of erythrocytes with Ehrlich ascites tumor cells.

Authors:  N Zakai; A Loyter; R G Kulka
Journal:  FEBS Lett       Date:  1974-04-01       Impact factor: 4.124

5.  The mechanism of cell fusion. II. Formation of chicken erythrocyte polykaryons.

Authors:  Z Toister; A Loyter
Journal:  J Biol Chem       Date:  1973-01-25       Impact factor: 5.157

6.  A new method for reconstitution of highly fusogenic Sendai virus envelopes.

Authors:  A Vainstein; M Hershkovitz; S Israel; S Rabin; A Loyter
Journal:  Biochim Biophys Acta       Date:  1984-06-27

7.  Fusogenic reconstituted Sendai virus envelopes as a vehicle for introducing DNA into viable mammalian cells.

Authors:  A Vainstein; A Razin; A Graessmann; A Loyter
Journal:  Methods Enzymol       Date:  1983       Impact factor: 1.600

8.  Active function of membrane receptors for enveloped viruses. I. Specific requirement for liposome-associated sialoglycolipids, but not sialoglycoproteins, to allow lysis of phospholipid vesicles by reconstituted Sendai viral envelopes.

Authors:  V Citovsky; N Zakai; A Loyter
Journal:  Exp Cell Res       Date:  1986-10       Impact factor: 3.905

9.  Reconstitution of functional influenza virus envelopes and fusion with membranes and liposomes lacking virus receptors.

Authors:  O Nussbaum; M Lapidot; A Loyter
Journal:  J Virol       Date:  1987-07       Impact factor: 5.103

10.  Targeting of loaded Sendai virus envelopes by covalently attached insulin molecules to virus receptor-depleted cells: fusion-mediated microinjection of ricin A and simian virus 40 DNA.

Authors:  A G Gitman; A Graessmann; A Loyter
Journal:  Proc Natl Acad Sci U S A       Date:  1985-11       Impact factor: 11.205

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