Department of Clinical and Experimental Medicine, University of Parma, Parma, Italy.
Virology. 2013 May 25;440(1):19-30. doi: 10.1016/j.virol.2013.01.021. Epub 2013 Mar 13.
Suitable host cell metabolic conditions are fundamental for the effective development of the human cytomegalovirus (HCMV) lytic cycle. Indeed, several studies have demonstrated the ability of this virus to interfere with cell cycle regulation, mainly by blocking proliferating cells in G1 or G1/S. In the present study, we demonstrate that HCMV deregulates the cell cycle of THP-1 macrophages (a cell line irreversibly arrested in G0) by pushing them into S and G2 phases. Moreover, we show that HCMV infection of THP-1 macrophages leads to Toll-like receptor 4 (TLR4) activation. Since various studies have indicated TLR4 to be involved in promoting cell proliferation, here we investigate the possible role of TLR4 in the observed HCMV-induced cell cycle perturbation. Our data strongly support TLR4 as a mediator of HCMV-triggered cell cycle activation in THP-1 macrophages favouring, in turn, the development of an efficient viral lytic cycle.
合适的宿主细胞代谢条件是人类巨细胞病毒 (HCMV) 裂解周期有效发展的基础。事实上,多项研究表明,该病毒能够干扰细胞周期调控,主要通过阻止 G1 或 G1/S 期的增殖细胞。在本研究中,我们证明 HCMV 通过将 THP-1 巨噬细胞(一种不可逆地停滞在 G0 期的细胞系)推向 S 和 G2 期来扰乱细胞周期。此外,我们表明 HCMV 感染 THP-1 巨噬细胞会导致 Toll 样受体 4 (TLR4) 的激活。由于多项研究表明 TLR4 参与促进细胞增殖,因此我们在此研究 TLR4 在观察到的 HCMV 诱导的细胞周期扰动中的可能作用。我们的数据强烈支持 TLR4 作为 HCMV 触发的 THP-1 巨噬细胞细胞周期激活的介质,从而有利于有效的病毒裂解周期的发展。