Reactive oxygen species‐induced parthanatos of immunocytes by human cytomegalovirus‐associated substance |
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| Authors: | Jung Heon Kim Jiyeon Kim Jin Roh Chan‐Sik Park Ju‐Young Seoh Eung‐Soo Hwang |
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| Affiliation: | 1. Department of Microbiology and Immunology, Seoul National University College of Medicine, 103 Daehak‐ro, Jongno‐gu, Seoul 03080, Korea;2. Institute of Endemic Diseases, Seoul National University College of Medicine, 103 Daehak‐ro, Jongno‐gu, Seoul 03080, Korea;3. Department of Pathology, University of Ulsan College of Medicine, Asan Medical Center, Seoul 05505, Korea;4. Department of Microbiology, Ehwa Womans University Graduate School of Medicine, Seoul 07985, Korea |
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| Abstract: | Previous studies have examined various immune evasion strategies of human cytomegalovirus (HCMV) to gain understanding of its pathogenesis. Although the mechanism that underlies immunocyte destruction near HCMV‐infected lesions has yet to be established, it is here shown that substances produced by HCMV‐infected cells induce death in several types of immunocytes, but not in fibroblasts or astrocytomas. These substances contain HCMV proteins and were termed HCMV‐associated insoluble substance (HCMVAIS). The mechanism by which HCMVAIS induces cell death was characterized to improve understanding the death of immunocytes near HCMV‐infected lesions. HCMVAIS were found to trigger production of intracellular nicotinamide adenine dinucleotide phosphate oxidase‐derived reactive oxygen species (ROS), resulting in cell death, this effect being reversed following treatment with ROS inhibitors. Cell death was not induced in splenocytes from NOX‐2 knockout mice. It was hypothesized that DNA damage induced by oxidative stress initiates poly ADP‐ribose polymerase‐1 (PARP‐1)‐mediated cell death, or parthanatos. HCMVAIS‐induced cell death is accompanied by PARP‐1 activation in a caspase‐independent manner, nuclear translocation of apoptosis‐inducing factor (AIF), and DNA fragmentation, which are typical features of parthanatos. Treatment with an AIF inhibitor decreased the rate of HCMVAIS‐induced cell death, this being confirmed by hematoxylin and eosin staining; cell death in most HCMV‐positive foci in serial section samples of a large intestine with HCMV infection was TUNEL‐positive, cleaved caspase 3‐negative and CD45‐positive. Taken together, these data suggest that HCMV inhibits local immune responses via direct killing of immunocytes near HCMV‐infected cells through ROS‐induced parthanatos by HCMVAIS. |
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| Keywords: | human cytomegalovirus parthanatos reactive oxygen species |
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