Literature DB >> 1827845

The E1B 19,000-molecular-weight protein of group C adenoviruses prevents tumor necrosis factor cytolysis of human cells but not of mouse cells.

L R Gooding1, L Aquino, P J Duerksen-Hughes, D Day, T M Horton, S P Yei, W S Wold.   

Abstract

Tumor necrosis factor (TNF) is a multifunctional immunoregulatory protein that is secreted by activated macrophages and is believed to have antiviral activities. We reported earlier that when mouse C3HA fibroblasts are infected with human adenoviruses, the 289R and 243R proteins encoded by region E1A render the cells susceptible to lysis by TNF, and a 14,700-molecular-weight protein (14.7K protein) encoded by region E3 protects the cells against lysis by TNF. We now report that the 19,000-molecular-weight (19K) (176R) protein encoded by the E1B transcription unit can protect human HEL-299 fibroblasts and human ME-180 cervical carcinoma cells against lysis by TNF. This was determined by infecting cells with adenovirus double mutants that lack region E3 and do or do not express the E1B-19K protein and by measuring cytolysis by using a short-term (18-h) 51Cr-release assay. Under these assay conditions, the 51Cr release was specific to TNF and was not a consequence of the cyt phenotype associated with E1B-19K protein-negative mutants. Also, by using virus double mutants that lack E3 in combination with other early regions, we found that E1A, the E1B-55K protein-encoding gene, E3, and E4 are not required to protect HEL-299 cells against TNF cytolysis. Three additional human cancer cell lines (HeLa, HCT8, and RC29) and a simian virus 40-transformed WI38 cell line (VA-13) also required E1B for protection against TNF cytolysis, indicating that the E1B-19K protein is required to protect many if not all human cell types against lysis by TNF when infected by adenovirus. The E1B-19K protein was not able to protect six different adenovirus-infected mouse cell lines against TNF lysis, even though the protein was shown to be efficiently expressed in one of the cell lines. HEL-299 or ME-180 cells infected by a mutant that lacks the E1B-19K protein but retains region E3 were not lysed by TNF, indicating that one or more of the E3 proteins can protect these cells against TNF lysis in the absence of the E1B-19K protein. Thus, the E3-14.7K but not the E1B-19K protein can protect adenovirus-infected mouse cells against TNF cytolysis, whereas the E1B-19K protein as well as one or more of the E3 proteins can protect adenovirus-infected human cells against TNF cytolysis.

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Year:  1991        PMID: 1827845      PMCID: PMC240964     

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  93 in total

1.  The repression of the growth factor-inducible genes JE, c-myc and stromelysin by adenovirus E1A is mediated by conserved region 1.

Authors:  H van Dam; R Offringa; A M Smits; J L Bos; N C Jones; A J van der Eb
Journal:  Oncogene       Date:  1989-10       Impact factor: 9.867

2.  Adenovirus E1B 19-kilodalton protein overcomes the cytotoxicity of E1A proteins.

Authors:  E White; R Cipriani; P Sabbatini; A Denton
Journal:  J Virol       Date:  1991-06       Impact factor: 5.103

3.  The adenovirus E3-14.7K protein is a general inhibitor of tumor necrosis factor-mediated cytolysis.

Authors:  L R Gooding; I O Sofola; A E Tollefson; P Duerksen-Hughes; W S Wold
Journal:  J Immunol       Date:  1990-11-01       Impact factor: 5.422

4.  Adenovirus transforming 19-kD T antigen has an enhancer-dependent trans-activation function and relieves enhancer repression mediated by viral and cellular genes.

Authors:  K Yoshida; L Venkatesh; M Kuppuswamy; G Chinnadurai
Journal:  Genes Dev       Date:  1987-09       Impact factor: 11.361

5.  An adenovirus 2-coded tumor antigen located on the endoplasmic reticulum and nuclear envelope is required for growth of transformed cells in Ca2+-deficient media.

Authors:  T Subramanian; M Kuppuswamy; G Chinnadurai
Journal:  Mol Cell Biol       Date:  1985-11       Impact factor: 4.272

6.  Induction of a cellular enzyme for energy metabolism by transforming domains of adenovirus E1a.

Authors:  R Kaddurah-Daouk; J W Lillie; G H Daouk; M R Green; R Kingston; P Schimmel
Journal:  Mol Cell Biol       Date:  1990-04       Impact factor: 4.272

7.  Induction of sensitivity to the cytotoxic action of tumor necrosis factor alpha by adenovirus E1A is independent of transformation and transcriptional activation.

Authors:  R S Ames; B Holskin; M Mitcho; D Shalloway; M J Chen
Journal:  J Virol       Date:  1990-09       Impact factor: 5.103

8.  Adenovirus E3 14.7K protein functions in the absence of other adenovirus proteins to protect transfected cells from tumor necrosis factor cytolysis.

Authors:  T M Horton; T S Ranheim; L Aquino; D I Kusher; S K Saha; C F Ware; W S Wold; L R Gooding
Journal:  J Virol       Date:  1991-05       Impact factor: 5.103

9.  The amino-terminal portion of CD1 of the adenovirus E1A proteins is required to induce susceptibility to tumor necrosis factor cytolysis in adenovirus-infected mouse cells.

Authors:  P J Duerksen-Hughes; T W Hermiston; W S Wold; L R Gooding
Journal:  J Virol       Date:  1991-03       Impact factor: 5.103

10.  Epidermal growth factor receptor is down-regulated by a 10,400 MW protein encoded by the E3 region of adenovirus.

Authors:  C R Carlin; A E Tollefson; H A Brady; B L Hoffman; W S Wold
Journal:  Cell       Date:  1989-04-07       Impact factor: 41.582

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  39 in total

1.  Bak and Bax function to limit adenovirus replication through apoptosis induction.

Authors:  Andrea Cuconati; Kurt Degenhardt; Ramya Sundararajan; Alan Anschel; Eileen White
Journal:  J Virol       Date:  2002-05       Impact factor: 5.103

2.  Tumor necrosis factor alpha plays a central role in immune-mediated clearance of adenoviral vectors.

Authors:  K B Elkon; C C Liu; J G Gall; J Trevejo; M W Marino; K A Abrahamsen; X Song; J L Zhou; L J Old; R G Crystal; E Falck-Pedersen
Journal:  Proc Natl Acad Sci U S A       Date:  1997-09-02       Impact factor: 11.205

3.  The adenovirus E1A proteins induce apoptosis, which is inhibited by the E1B 19-kDa and Bcl-2 proteins.

Authors:  L Rao; M Debbas; P Sabbatini; D Hockenbery; S Korsmeyer; E White
Journal:  Proc Natl Acad Sci U S A       Date:  1992-08-15       Impact factor: 11.205

4.  Responses of insect cells to baculovirus infection: protein synthesis shutdown and apoptosis.

Authors:  X Du; S M Thiem
Journal:  J Virol       Date:  1997-10       Impact factor: 5.103

5.  Identification of a new human adenovirus protein encoded by a novel late l-strand transcription unit.

Authors:  Ann E Tollefson; Baoling Ying; Konstantin Doronin; Peter D Sidor; William S M Wold
Journal:  J Virol       Date:  2007-09-19       Impact factor: 5.103

6.  Adenovirus E1B 19-kilodalton protein overcomes the cytotoxicity of E1A proteins.

Authors:  E White; R Cipriani; P Sabbatini; A Denton
Journal:  J Virol       Date:  1991-06       Impact factor: 5.103

7.  Adenovirus inhibition of cell translation facilitates release of virus particles and enhances degradation of the cytokeratin network.

Authors:  Y Zhang; R J Schneider
Journal:  J Virol       Date:  1994-04       Impact factor: 5.103

8.  Human adenovirus type 37 and the BALB/c mouse: progress toward a restricted adenovirus keratitis model (an American Ophthalmological Society thesis).

Authors:  James Chodosh
Journal:  Trans Am Ophthalmol Soc       Date:  2006

9.  Induction of apoptosis by human Nbk/Bik, a BH3-containing protein that interacts with E1B 19K.

Authors:  J Han; P Sabbatini; E White
Journal:  Mol Cell Biol       Date:  1996-10       Impact factor: 4.272

10.  Down-regulation of HLA antigens by the adenovirus type 2 E3/19K protein in a T-lymphoma cell line.

Authors:  H Körner; H G Burgert
Journal:  J Virol       Date:  1994-03       Impact factor: 5.103

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