Mechanisms for human cytomegalovirus-induced cytoplasmic p53 sequestration in endothelial cells

Budi Utama, Ying H. Shen, Bradley M. Mitchell, Irwan T. Makagiansar, Yehua Gan, Raveendran Muthuswamy, Senthil Duraisamy, David Martin, Xinwen Wang, Ming Xiang Zhang, Jing Wang, Jian Wang, Greg M. Vercellotti, Wei Gu, Xing Li Wang

Research output: Contribution to journalArticlepeer-review

15 Scopus citations


Human cytomegalovirus (HCMV) infection results in endothelial dysfunction, typically known as dysregulated apoptosis, and aberrant expression and sub-cellular localization of p53, a tumor suppressor that accumulates at the late stage of infection. In this study, we examined three hypotheses that could be responsible for HCMV-induced cytoplasmic p53 accumulation at the later stage of infection: hyperactive nuclear export, cytoplasmic p53 tethering and delayed p53 degradation. Leptomycin B treatment, a nuclear export inhibitor, was unable to reduce cytoplasmic p53, thereby eliminating the hyperactive nuclear export mechanism. The findings that nascent p53 still entered nuclei after the nuclear export inhibition indicated that cytoplasmic tethering may play a minor role. Cytoplasmic p53 was still observed after the translation activities were blocked by cycloheximide. There was more than an eight-fold increase in the cytoplasmic p53 half-life with abnormal p53 ubiquitination. Taken together, these results suggest that delayed degradation could be responsible for the cytoplasmic p53 accumulation. The general slow-down of the proteasomal activity and the dysregulated p53 ubiquitination process at the later stage of infection could contribute to the reduced cytoplasmic p53 degradation and might be relevant to dysregulated endothelial apoptosis. The HCMV-induced changes in p53 dynamics could contribute to endothelial dysfunction.

Original languageEnglish (US)
Pages (from-to)2457-2467
Number of pages11
JournalJournal of cell science
Issue number12
StatePublished - Jun 15 2006


  • Endothelial dysfunction
  • Human cytomegalovirus
  • p53


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