Literature DB >> 3007530

Sorting and endocytosis of viral glycoproteins in transfected polarized epithelial cells.

T A Gottlieb, A Gonzalez, L Rizzolo, M J Rindler, M Adesnik, D D Sabatini.   

Abstract

Previous studies (Rindler, M. J., I. E., Ivanov, H. Plesken, and D. D. Sabatini, 1985, J. Cell Biol., 100: 136-151; Rindler, M. J., I. E. Ivanov, H. Plesken, E. J. Rodriguez-Boulan, and D. D. Sabatini, 1984, J. Cell Biol., 98: 1304-1319) have demonstrated that in polarized Madin-Darby canine kidney cells infected with vesicular stomatitis virus (VSV) or influenza virus the viral envelope glycoproteins G and HA are segregated to the basolateral and apical plasma membrane domains, respectively, where budding of the corresponding viruses takes place. Furthermore, it has been shown that this segregation of the glycoproteins reflects the polarized delivery of the newly synthesized polypeptides to each surface domain. In transfection experiments using eukaryotic expression plasmids that contain cDNAs encoding the viral glycoproteins, it is now shown that even in the absence of other viral components, both proteins are effectively segregated to the appropriate cell surface domain. In transfected cells, the HA glycoprotein was almost exclusively localized in the apical cell surface, whereas the G protein, although preferentially localized in the basolateral domains, was also present in lower amounts, in the apical surfaces of many cells. Using transfected and infected cells, it was demonstrated that, after reaching the cell surface, the G protein, but not the HA protein, undergoes interiorization by endocytosis. Thus, in the presence of chloroquine, a drug that blocks return of interiorized plasma membrane proteins to the cell surface, the G protein was quantitatively trapped in endosome- or lysosome-like vesicles. The sequestration of G was a rapid process that was completed in many cells by 1-2 h after chloroquine treatment. The fact that in transfected cells the surface content of G protein was not noticeably reduced during a 5-h incubation with cycloheximide, a protein synthesis inhibitor that did not prevent the effect of chloroquine, implies that normally, G protein molecules are not only interiorized but are also recycled to the cell surface.

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Year:  1986        PMID: 3007530      PMCID: PMC2114186          DOI: 10.1083/jcb.102.4.1242

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  43 in total

1.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

2.  Expression of recombinant plasmids in mammalian cells is enhanced by sodium butyrate.

Authors:  C M Gorman; B H Howard; R Reeves
Journal:  Nucleic Acids Res       Date:  1983-11-11       Impact factor: 16.971

3.  Vesicular stomatitis virus infects and matures only through the basolateral surface of the polarized epithelial cell line, MDCK.

Authors:  S Fuller; C H von Bonsdorff; K Simons
Journal:  Cell       Date:  1984-08       Impact factor: 41.582

4.  Intracellular transport of influenza virus hemagglutinin to the apical surface of Madin-Darby canine kidney cells.

Authors:  E Rodriguez-Boulan; K T Paskiet; P J Salas; E Bard
Journal:  J Cell Biol       Date:  1984-01       Impact factor: 10.539

5.  Sorting of an apical plasma membrane glycoprotein occurs before it reaches the cell surface in cultured epithelial cells.

Authors:  K S Matlin; K Simons
Journal:  J Cell Biol       Date:  1984-12       Impact factor: 10.539

6.  Biosynthesis and intracellular sorting of growth hormone-viral envelope glycoprotein hybrids.

Authors:  L J Rizzolo; J Finidori; A Gonzalez; M Arpin; I E Ivanov; M Adesnik; D D Sabatini
Journal:  J Cell Biol       Date:  1985-10       Impact factor: 10.539

7.  Cell surface expression of fusogenic vesicular stomatitis virus G protein from cloned cDNA.

Authors:  H Riedel; C Kondor-Koch; H Garoff
Journal:  EMBO J       Date:  1984-07       Impact factor: 11.598

8.  Expression of Semliki Forest virus proteins from cloned complementary DNA. I. The fusion activity of the spike glycoprotein.

Authors:  C Kondor-Koch; B Burke; H Garoff
Journal:  J Cell Biol       Date:  1983-09       Impact factor: 10.539

9.  Viral glycoproteins destined for apical or basolateral plasma membrane domains traverse the same Golgi apparatus during their intracellular transport in doubly infected Madin-Darby canine kidney cells.

Authors:  M J Rindler; I E Ivanov; H Plesken; E Rodriguez-Boulan; D D Sabatini
Journal:  J Cell Biol       Date:  1984-04       Impact factor: 10.539

10.  Recycling of the asialoglycoprotein receptor and the effect of lysosomotropic amines in hepatoma cells.

Authors:  A L Schwartz; A Bolognesi; S E Fridovich
Journal:  J Cell Biol       Date:  1984-02       Impact factor: 10.539

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  30 in total

1.  Basement membrane stimulates the polarized distribution of integrins but not the Na,K-ATPase in the retinal pigment epithelium.

Authors:  L J Rizzolo
Journal:  Cell Regul       Date:  1991-11

2.  Endosomal KATP channels as a reservoir after myocardial ischemia: a role for SUR2 subunits.

Authors:  Li Bao; Krassimira Hadjiolova; William A Coetzee; Michael J Rindler
Journal:  Am J Physiol Heart Circ Physiol       Date:  2010-10-22       Impact factor: 4.733

3.  Rotavirus is released from the apical surface of cultured human intestinal cells through nonconventional vesicular transport that bypasses the Golgi apparatus.

Authors:  N Jourdan; M Maurice; D Delautier; A M Quero; A L Servin; G Trugnan
Journal:  J Virol       Date:  1997-11       Impact factor: 5.103

4.  An internalized transmembrane protein resides in a fusion-competent endosome for less than 5 minutes.

Authors:  J Gruenberg; K E Howell
Journal:  Proc Natl Acad Sci U S A       Date:  1987-08       Impact factor: 11.205

5.  Intracellular processing and transport of influenza-virus envelope proteins in Madin-Darby canine kidney cells. Effects of the carboxylic ionophores monensin and nigericin.

Authors:  P U Daniels; J M Edwardson
Journal:  Biochem J       Date:  1988-06-15       Impact factor: 3.857

6.  Possible involvement of microtubule disruption in bipolar budding of a Sendai virus mutant, F1-R, in epithelial MDCK cells.

Authors:  M Tashiro; J T Seto; H D Klenk; R Rott
Journal:  J Virol       Date:  1993-10       Impact factor: 5.103

7.  Nonpolarized secretion of truncated forms of the influenza hemagglutinin and the vesicular stomatitus virus G protein from MDCK cells.

Authors:  A Gonzalez; L Rizzolo; M Rindler; M Adesnik; D D Sabatini; T Gottlieb
Journal:  Proc Natl Acad Sci U S A       Date:  1987-06       Impact factor: 11.205

8.  Exploitation of nucleic acid packaging signals to generate a novel influenza virus-based vector stably expressing two foreign genes.

Authors:  Tokiko Watanabe; Shinji Watanabe; Takeshi Noda; Yutaka Fujii; Yoshihiro Kawaoka
Journal:  J Virol       Date:  2003-10       Impact factor: 5.103

9.  Apical and basolateral endosomes of MDCK cells are interconnected and contain a polarized sorting mechanism.

Authors:  G Odorizzi; A Pearse; D Domingo; I S Trowbridge; C R Hopkins
Journal:  J Cell Biol       Date:  1996-10       Impact factor: 10.539

10.  Migration of Nucleocapsids in Vesicular Stomatitis Virus-Infected Cells Is Dependent on both Microtubules and Actin Filaments.

Authors:  Shalane K Yacovone; Amanda M Smelser; Jed C Macosko; George Holzwarth; David A Ornelles; Douglas S Lyles
Journal:  J Virol       Date:  2016-06-10       Impact factor: 5.103

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