Similar activation of signal transduction pathways by the herpesvirus-encoded chemokine receptors US28 and ORF74

TY - JOUR

T1 - Similar activation of signal transduction pathways by the herpesvirus-encoded chemokine receptors US28 and ORF74

AU - McLean, Katherine A

AU - Holst, Peter J

AU - Martini, Lene

AU - Schwartz, Thue W

AU - Rosenkilde, Mette M

N1 - Keywords: Animals; Blood Vessels; COS Cells; Cell Line; Chemokines; Cyclic AMP Response Element-Binding Protein; Cytomegalovirus; DNA-Binding Proteins; Herpesvirus 8, Human; Humans; Inflammation; NFATC Transcription Factors; Nuclear Proteins; Receptors, Chemokine; Signal Transduction; Transcription Factors; Transcriptional Activation; Viral Proteins

PY - 2004

Y1 - 2004

N2 - The virally encoded chemokine receptors US28 from human cytomegalovirus and ORF74 from human herpesvirus 8 are both constitutively active. We show that both receptors constitutively activate the transcription factors nuclear factor of activated T cells (NFAT) and cAMP response element binding protein (CREB) and that both pathways are modulated by their respective endogenous receptor ligands. By addition of specific pathway modulators against the G protein subunit Galphai, phospholipase C, protein kinase C, calcineurin, p38 MAP kinase, and MEK1, we find that the constitutive and ligand-dependent inductions are mediated by multiple yet similar pathways in both receptors. The NFAT and CREB transcription factors and their upstream activators are known inducers of host and virally encoded genes. We propose that the activity of these virally encoded chemokine receptors coordinates host and potentially viral gene expression similarly. As ORF74 is a known inducer of neoplasia, these findings may have important implications for cytomegalovirus-associated pathogenicity.

AB - The virally encoded chemokine receptors US28 from human cytomegalovirus and ORF74 from human herpesvirus 8 are both constitutively active. We show that both receptors constitutively activate the transcription factors nuclear factor of activated T cells (NFAT) and cAMP response element binding protein (CREB) and that both pathways are modulated by their respective endogenous receptor ligands. By addition of specific pathway modulators against the G protein subunit Galphai, phospholipase C, protein kinase C, calcineurin, p38 MAP kinase, and MEK1, we find that the constitutive and ligand-dependent inductions are mediated by multiple yet similar pathways in both receptors. The NFAT and CREB transcription factors and their upstream activators are known inducers of host and virally encoded genes. We propose that the activity of these virally encoded chemokine receptors coordinates host and potentially viral gene expression similarly. As ORF74 is a known inducer of neoplasia, these findings may have important implications for cytomegalovirus-associated pathogenicity.

U2 - 10.1016/j.virol.2004.04.027

DO - 10.1016/j.virol.2004.04.027

M3 - Journal article

C2 - 15246264

SN - 0042-6822

VL - 325

SP - 241

EP - 251

JO - Virology

JF - Virology

IS - 2

ER -