Dietary sodium modulates mTORC1-dependent trained immunity in macrophages to accelerate CKD development

IF 5.3 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Huihui Chen , Jie Song , Li Zeng , Jie Zha , Jiefu Zhu , Anqun Chen , Yu Liu , Zheng Dong , Guochun Chen
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Abstract

Chronic Kidney Disease (CKD) is a significant global health issue linked to dietary habits, especially high salt intake. However, the precise mechanisms driving this progression remain incompletely understood. This study reveals that a high-salt diet intensifies macrophage trained immunity, leading to a marked pro-inflammatory response upon repeated pathogenic exposures, as evidenced by increased renal damage and fibrosis. Under high-salt conditions, there was an induction of CD45+F4/80+ macrophage infiltration into the renal tissue, accompanied by heightened production of inflammatory cytokines. Distinct responses were observed between circulating and resident renal macrophages to a high-salt diet, with a notable upsurge in the migration of pro-inflammatory macrophages, driven by CCL2-CCR2 signaling and aberrant mTORC1 pathway activation. Treatment with rapamycin-liposome effectively reduced this inflammatory cascade by mitigating mTORC1 signaling. Transplantation of monocytes from CKD mice with a high-salt diet significantly exacerbates renal inflammatory damage in the host mice, showing increased migratory tendency and inflammatory activity. The cell co-culture experiment further confirmed that macrophages derived from CKD mice, particularly those under conditions of high salt exposure, significantly induced apoptosis and inflammatory responses in renal tubular cells. Taken together, recurrent exposure to LPS elicits the activation of trained immunity, consequently augmenting inflammatory response of monocytes/macrophages in the involved kidneys. The high-salt diet exacerbates this phenomenon, attributable at least in part to the overactivation of the mTORC1 pathway. This research emphasizes the importance of dietary modulation and targeted immunological interventions in slowing CKD progression, providing new insights into mTORC1-mediated pathophysiological mechanisms and potential management strategies for CKD.

Abstract Image

饮食中的钠会调节巨噬细胞中依赖于 mTORC1 的训练有素的免疫力,从而加速慢性肾脏病的发展
慢性肾脏病(CKD)是与饮食习惯,尤其是高盐摄入量有关的全球重大健康问题。然而,人们对这一疾病进展的确切机制仍不甚了解。这项研究揭示了高盐饮食会增强巨噬细胞训练有素的免疫力,从而在反复接触致病因素时导致明显的促炎反应,肾脏损伤和纤维化的加剧就是证明。在高盐条件下,诱导 CD45+F4/80+ 巨噬细胞浸润肾组织,并伴随着炎症细胞因子分泌的增加。在 CCL2-CCR2 信号和异常 mTORC1 通路激活的驱动下,促炎巨噬细胞的迁移显著增加。使用雷帕霉素脂质体治疗可通过减轻 mTORC1 信号传导有效减少这种炎症级联反应。移植高盐饮食的 CKD 小鼠的单核细胞会明显加重宿主小鼠的肾脏炎症损伤,表现出更强的迁移倾向和炎症活性。细胞共培养实验进一步证实,来自 CKD 小鼠的巨噬细胞,尤其是在高盐暴露条件下的巨噬细胞,能明显诱导肾小管细胞的凋亡和炎症反应。综上所述,反复暴露于 LPS 会激活训练有素的免疫系统,从而增强受累肾脏中单核细胞/巨噬细胞的炎症反应。高盐饮食加剧了这一现象,这至少部分归因于 mTORC1 通路的过度激活。这项研究强调了饮食调节和有针对性的免疫学干预在延缓慢性肾脏病进展方面的重要性,为 mTORC1 介导的病理生理机制和潜在的慢性肾脏病管理策略提供了新的见解。
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来源期刊
Biochemical pharmacology
Biochemical pharmacology 医学-药学
CiteScore
10.30
自引率
1.70%
发文量
420
审稿时长
17 days
期刊介绍: Biochemical Pharmacology publishes original research findings, Commentaries and review articles related to the elucidation of cellular and tissue function(s) at the biochemical and molecular levels, the modification of cellular phenotype(s) by genetic, transcriptional/translational or drug/compound-induced modifications, as well as the pharmacodynamics and pharmacokinetics of xenobiotics and drugs, the latter including both small molecules and biologics. The journal''s target audience includes scientists engaged in the identification and study of the mechanisms of action of xenobiotics, biologics and drugs and in the drug discovery and development process. All areas of cellular biology and cellular, tissue/organ and whole animal pharmacology fall within the scope of the journal. Drug classes covered include anti-infectives, anti-inflammatory agents, chemotherapeutics, cardiovascular, endocrinological, immunological, metabolic, neurological and psychiatric drugs, as well as research on drug metabolism and kinetics. While medicinal chemistry is a topic of complimentary interest, manuscripts in this area must contain sufficient biological data to characterize pharmacologically the compounds reported. Submissions describing work focused predominately on chemical synthesis and molecular modeling will not be considered for review. While particular emphasis is placed on reporting the results of molecular and biochemical studies, research involving the use of tissue and animal models of human pathophysiology and toxicology is of interest to the extent that it helps define drug mechanisms of action, safety and efficacy.
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