Plasmacytoid dendritic cells promote acute kidney injury by producing interferon-α.

Abstract

Acute kidney injury (AKI) is a common clinical complication associated with high mortality in patients. Immune cells and cytokines have recently been described to play essential roles in AKI pathogenesis. Plasmacytoid dendritic cells (pDCs) are a unique DC subset that specializes in type I interferon (IFN) production. Here, we showed that pDCs rapidly infiltrated the kidney in response to AKI and contributed to kidney damage by producing IFN-α. Deletion of pDCs using DTRBDCA2 transgenic (Tg) mice suppressed cisplatin-induced AKI, accompanied by marked reductions in proinflammatory cytokine production, immune cell infiltration and apoptosis in the kidney. In contrast, adoptive transfer of pDCs during AKI exacerbated kidney damage. We further identified IFN-α as the key factor that mediated the functions of pDCs during AKI, as IFN-α neutralization significantly attenuated kidney injury. Furthermore, IFN-α produced by pDCs directly induced the apoptosis of renal tubular epithelial cells (TECs) in vitro. In addition, our data demonstrated that apoptotic TECs induced the activation of pDCs, which was inhibited in the presence of an apoptosis inhibitor. Furthermore, similar deleterious effects of pDCs were observed in an ischemia reperfusion (IR)-induced AKI model. Clinically, increased expression of IFN-α in kidney biopsies was observed in kidney transplants with AKI. Taken together, the results of our study reveal that pDCs play a detrimental role in AKI via IFN-α.

• Authors: Bo Deng, Yuli Lin, Yusheng Chen, Shuai Ma, Qian Cai, Wenji Wang, Bingji Li, Tingyan Liu, Peihui Zhou, Rui He, Feng Ding
• Journal: Cellular & molecular immunology (Cell Mol Immunol) Vol. 18 Issue 1 Pg. 219-229 (01 2021) ISSN: 2042-0226 [Electronic] China
• PMID: 31900458 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Cross-Linking Reagents
• Interferon-alpha
• Cisplatin

Topics

• Acute Kidney Injury (chemically induced, metabolism, pathology)
• Animals
• Cisplatin (toxicity)
• Cross-Linking Reagents (toxicity)
• Dendritic Cells (immunology)
• Interferon-alpha (metabolism)
• Male
• Mice
• Mice, Inbred C57BL