RIP1 kinase activity promotes steatohepatitis through mediating cell death and inflammation in macrophages

Abstract Hepatocyte cell death and liver inflammation have been well recognized as central characteristics of nonalcoholic steatohepatitis (NASH), however, the underlying molecular basis remains elusive. The kinase receptor-interacting protein 1 (RIP1) is a key regulator of apoptosis, necroptosis and inflammation, we thus hypothesized that the kinase activity of RIP1 may be involved in the pathogenesis of NASH. Wild-type and RIP1 kinase-dead (Rip1K45A/K45A) mice were fed with methionine-and choline-deficient diet (MCD) or high-fat diet (HFD) to establish distinct NASH models. In both models, compared to WT mice, Rip1K45A/K45A mice exhibited significantly less liver injury, less steatosis, decreased inflammation, and less cell death in liver tissue. Moreover, hepatic fibrosis as characterized by Sirius Red staining, expression of α-SMA and other fibrosis markers, were significantly alleviated in Rip1K45A/K45A mice than WT controls. Furthermore, using bone marrow transplantation to create chimeric mice, we found that it is the RIP1 kinase in hematopoietic-derived macrophages contributing mostly to the disease progression in NASH. Results from in vitro studies were in agreement with the in vivo data, demonstrating that RIP1 kinase was required for inflammasome activation and cell death induced by saturated fatty acid (palmitic acid) in bone marrow-derived macrophages (BMDMs). At last, we also found that the phosphorylation and expression of RIP1 was obviously increased in patients with NAFLD or NASH, but not in healthy controls. In summary, our results indicate that RIP1 kinase is activated during the pathogenesis of steatohepatitis, and consequently induces inflammation and cell death in macrophages, contributing to the disease progression. Our study suggests that macrophage RIP1 kinase represents a specific and potential target for the treatment of NASH..

Medienart:	Preprint

Erscheinungsjahr:	2020
Erschienen:	2020

Enthalten in:	bioRxiv.org - (2020) vom: 08. Dez. Zur Gesamtaufnahme - year:2020

Sprache:	Englisch

Beteiligte Personen:

Tao, Liang [VerfasserIn] Yi, Yuguo [VerfasserIn] Chen, Yuxin [VerfasserIn] Zhang, Haibing [VerfasserIn] Jie, Jiapeng [VerfasserIn] Zhang, Weigao [VerfasserIn] Xu, Qian [VerfasserIn] Li, Yang [VerfasserIn] Orning, Pontus [VerfasserIn] Lien, Egil [VerfasserIn] Zhao, Mengshu [VerfasserIn] Gao, Pingshi [VerfasserIn] Ling, Ling [VerfasserIn] Ding, Zhao [VerfasserIn] Wu, Chao [VerfasserIn] Ding, Qiurong [VerfasserIn] Wang, Junsong [VerfasserIn] Zhang, Jianfa [VerfasserIn] Weng, Dan [VerfasserIn]

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doi:	10.1101/2020.01.07.895516

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PPN (Katalog-ID):	XBI000695130