J Gen Virol Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Gen Virol 75 (1994), 3319-3325; DOI 10.1099/0022-1317-75-12-3319
© 1994 Society for General Microbiology

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Warren, A. P.
Right arrow Articles by Patel, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Warren, A. P.
Right arrow Articles by Patel, K.
Agricola
Right arrow Articles by Warren, A. P.
Right arrow Articles by Patel, K.

Down-regulation of integrin {alpha}1/beta1 expression and association with cell rounding in human cytomegalovirus-infected fibroblasts

A. P. Warren{dagger}, C. N. Owens, L. K. Borysiewicz and K. Patel{dagger}

Department of Medicine, University of Wales College of Medicine, Heath Park, Cardiff CF4 4XN, U.K.

Human cytomegalovirus (HCMV) causes a c.p.e. characterized by rounding of the infected cell. Since interactions with the extracellular matrix may be involved in the cell rounding, we have analysed the expression of integrins, which are the main cell surface receptors involved in cell-substrate adhesion and spreading. By FACS analysis, a selective decrease in cell surface expression of {alpha}1/beta1 integrin was observed in HCMV-infected fibroblasts. This decrease coincides with cell rounding. Immunoprecipitation studies and FACS analysis of permeabilized cells have further demonstrated that total levels of this integrin are decreased in infected cells, suggesting that the reduction in cell surface {alpha}1/beta1 integrin is not due to a defect in transport to the surface. Furthermore, we have ruled out the possibility that the observed decrease in {alpha}1/beta1 expression is caused by a cytokine released from the infected cells by showing that the reduction is abolished by inactivating the HCMV with u.v. irradiation, and that conditioned medium from HCMV-infected cells has no effect on expression of {alpha}1/beta1 integrin in uninfected cells. Concomitant with the reduction in {alpha}1/beta1 levels, the HCMV-infected fibroblasts show a reduced ability to adhere to laminin and collagen IV. Taken together the data indicate that de novo synthesis of HCMV protein(s) causes a decreased assembly/expression of {alpha}1/beta1 integrin, coincident with the well characterized morphological alterations of the infected cell.

{dagger} Present address: Department of Immunology, M. D. Anderson Cancer Centre, The University of Texas, Texas Medical Centre, 1515 Holcombe Boulevard, Houston, Texas 77030, U.S.A.

Received 20 January 1994; accepted 9 August 1994.


This article has been cited by other articles:


Home page
J. Immunol.Home page
G. Chan, E. R. Bivins-Smith, M. S. Smith, P. M. Smith, and A. D. Yurochko
Transcriptome Analysis Reveals Human Cytomegalovirus Reprograms Monocyte Differentiation toward an M1 Macrophage
J. Immunol., July 1, 2008; 181(1): 698 - 711.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
P. Halasz, G. Holloway, S. J. Turner, and B. S. Coulson
Rotavirus Replication in Intestinal Cells Differentially Regulates Integrin Expression by a Phosphatidylinositol 3-Kinase-Dependent Pathway, Resulting in Increased Cell Adhesion and Virus Yield
J. Virol., January 1, 2008; 82(1): 148 - 160.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
R. J. Stanton, B. P. McSharry, C. R. Rickards, E. C. Y. Wang, P. Tomasec, and G. W. G. Wilkinson
Cytomegalovirus Destruction of Focal Adhesions Revealed in a High-Throughput Western Blot Analysis of Cellular Protein Expression
J. Virol., August 1, 2007; 81(15): 7860 - 7872.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Biol.Home page
D. Poncet, A.-L. Pauleau, G. Szabadkai, A. Vozza, S. R. Scholz, M. Le Bras, J.-J. Briere, A. Jalil, R. Le Moigne, C. Brenner, et al.
Cytopathic effects of the cytomegalovirus-encoded apoptosis inhibitory protein vMIA
J. Cell Biol., September 25, 2006; 174(7): 985 - 996.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
L. Hertel and E. S. Mocarski
Global Analysis of Host Cell Gene Expression Late during Cytomegalovirus Infection Reveals Extensive Dysregulation of Cell Cycle Gene Expression and Induction of Pseudomitosis Independent of US28 Function
J. Virol., November 1, 2004; 78(21): 11988 - 12011.
[Abstract] [Full Text] [PDF]


Home page
Physiol. GenomicsHome page
J. F. Challacombe, A. Rechtsteiner, R. Gottardo, L. M. Rocha, E. P. Browne, T. Shenk, M. R. Altherr, and T. S. Brettin
Evaluation of the host transcriptional response to human cytomegalovirus infection
Physiol Genomics, June 17, 2004; 18(1): 51 - 62.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 1994 by the Society for General Microbiology.