Àá½Ã¸¸ ±â´Ù·Á ÁÖ¼¼¿ä. ·ÎµùÁßÀÔ´Ï´Ù.
KMID : 0921620150450020159
Journal of Bacteriology and Virology
2015 Volume.45 No. 2 p.159 ~ p.164
Differential Regulation of NF-¥êB Signaling during Human Cytomegalovirus Infection
Kwon Ki-Mun

Ahn Jin-Hyun
Abstract
NF-¥êB transcription factors are key regulators of immune and stress responses, apoptosis, and differentiation. Human cytomegalovirus (HCMV) activates or represses NF-¥êB signaling at different times during infection. An initial increase in NF-¥êB activity occurs within a few hours of infection. The virus appears to adapt to this change since initial viral gene expression is promoted by the elevated NF-¥êB activity. Because NF-¥êB upregulates innate immune responses and inflammation, it has also been suggested that HCMV needs to downregulate NF-¥êB signaling. Recent studies have shown that HCMV has various mechanisms that inhibit NF-¥êB signaling. HCMV reduces cell surface expression of tumor necrosis factor receptor 1 (TNFR1) and blocks the DNA binding activity of NF-¥êB. Furthermore, some HCMV tegument proteins antagonize NF-¥êB activation by targeting the key components of NF-¥êB signaling at late stages of infection. In this review, we summarize the recent findings on the relationship between HCMV and NF-¥êB signaling, focusing, in particular, on the viral mechanisms by which the NF-¥êB signaling pathway is inhibited.
KEYWORD
Cytomegalovirus, NF-¥êB, Immune response, Tegument protein
FullTexts / Linksout information
 
Listed journal information
ÇмúÁøÈïÀç´Ü(KCI) KoreaMed