Neuropeptide Y protects kidney from acute kidney injury by inactivating M1 macrophages via the Y1R-NF-κB-Mincle-dependent mechanism

• Published in: International journal of biological sciences Vol. 19; no. 2; pp. 521 - 536
• Main Authors: Tan, Rui-zhi, Li, Jian-chun, Zhu, Bing-wen, Huang, Xiao-ru, Wang, Hong-lian, Jia, Jian, Zhong, Xia, Liu, Jian, Wang, Li, Lan, Hui-yao
• Format: Journal Article
• Language: English
• Published: Australia Ivyspring International Publisher Pty Ltd 2023; Ivyspring International Publisher
• Subjects: Acute Kidney Injury - chemically induced; Acute Kidney Injury - drug therapy; Animal models; Animals; Cell activation; Chemical compounds; Chemokines; Cisplatin; Cisplatin - pharmacology; Creatinine; Cytokines; Deactivation; Dendritic cells; Flow cytometry; Hypertension; Ischemia; Kidney - drug effects; Kidney - metabolism; Kidney diseases; Kidneys; Macrophages; Macrophages - drug effects; Macrophages - metabolism; Mice; Neuropeptide Y; Neuropeptide Y - metabolism; Neuropeptide Y - pharmacology; Neuropeptide Y - therapeutic use; Neuropeptides; NF-kappa B; NF-κB protein; Patients; Peptides; Pharmacology; Quantitative analysis; Receptors, Neuropeptide Y - metabolism; Renal function; Research Paper; Neuropeptide Y; Inflammation; Mincle; Y1R; AKI; Macrophage
• ISSN: 1449-2288; 1449-2288
• DOI: 10.7150/ijbs.80200

Neuropeptide Y (NPY) is produced by the nerve system and may contribute to the progression of CKD. The present study found the new protective role for NPY in AKI in both patients and animal models. Interestingly, NPY was constitutively expressed in blood and resident kidney macrophages by co-expressing NPY and CD68+ markers, which was lost in patients and mice with AKI-induced by cisplatin. Unexpectedly, NPY was renoprotective in AKI as mice lacking NPY developed worse renal necroinflammation and renal dysfunction in cisplatin and ischemic-induced AKI. Importantly, NPY was also a therapeutic agent for AKI because treatment with exogenous NPY dose-dependently inhibited cisplatin-induced AKI. Mechanistically, NPY protected kidney from AKI by inactivating M1 macrophages via the Y1R-NF-κB-Mincle-dependent mechanism as deleting or silencing NPY decreased Y1R but increased NF-κB-Mincle-mediated M1macrophage activation and renal necroinflammation, which were reversed by addition of NPY or by silencing Mincle but promoted by blocking Y1R with BIBP 3226. Thus, NPY is renoprotective and may be a novel therapeutic agent for AKI. NPY may act via Y1R to protect kidney from AKI by blocking NF-κB-Mincle-mediated M1 macrophage activation and renal necroinflammation.