口服多酶锰碳点通过肠-肺轴减轻败血症相关肺损伤。

IF 16 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
ACS Nano Pub Date : 2025-10-23 DOI:10.1021/acsnano.5c10625
Lei Peng,Honghao Song,Huijing Shi,Lixue Wu,Yuqing Ma,Xiaoyi Fan,Min Wu,Liwei Duan,Zhenjie Li,Hongbin Yuan
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引用次数: 0

摘要

脓毒症引起的肺损伤是一种危及生命的全球性健康挑战,其病理机制定义不清。肠-肺轴已被证明广泛参与败血症诱导的肺损伤,但针对肠道微生物群稳态的有效干预措施尚不清楚。单细胞测序显示脓毒症发病过程中肺泡凋亡增加,巨噬细胞efferocylosis受损。因此,我们设计了口服锰掺杂碳点(Mn-CDs),通过重塑肠道微生物群稳态和靶向肠-肺轴来减轻脓毒性肺损伤。生化表征表明Mn-CDs具有多酶模拟活性(SOD-, CAT-, POD-, gpx样)和强大的活性氧清除能力。在小鼠脓毒症模型中,经转录组分析证实,Mn-CDs显著改善了全身指标,并与巨噬细胞抗炎状态和efferocytosis增强相关。综合宏基因组学/代谢组学分析发现,mn - cds介导的g_Clostridium和g_Bacteroides富集伴随着吲哚-3-丙酸(IPA)产量的升高。随后的体外研究表明,IPA可能主要与芳烃受体(AHR)结合,促进巨噬细胞的efferocytosis和抗炎极化,从而减轻脓毒性肺损伤。值得注意的是,mn - cds处理小鼠的粪便微生物群移植(FMT)不仅缓解了全身症状,而且有效促进了脓毒症小鼠肺巨噬细胞的efferocytic极化。在脓毒性肺损伤小鼠模型中,肠道微生物群的耗竭导致Mn-CDs的保护作用显著丧失。总的来说,由微生物源性IPA和巨噬细胞efferocytosis介导的肠-肺轴有助于脓毒性肺损伤的修复,突出了Mn-CDs在微生物组导向的重症监护中的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Oral Multi-Enzymatic Manganese-Carbon Dots Alleviate Sepsis-Associated Lung Injury via the Gut-Lung Axis.
Sepsis-induced pulmonary injury represents a life-threatening global health challenge due to poorly defined pathological mechanisms. The gut-lung axis has been proven to be widely involved in sepsis-induced lung injury, yet effective interventions targeting gut microbiota homeostasis remain unknown. Single-cell sequencing revealed increased alveolar apoptosis and impaired macrophage efferocytosis during sepsis pathogenesis. Thus, we designed oral manganese-doped carbon dots (Mn-CDs) to alleviate septic lung injury by remodeling gut microbiota homeostasis and targeting the gut-lung axis. Biochemical characterization demonstrated Mn-CDs possess multienzyme mimetic activities (SOD-, CAT-, POD-, GPx-like) and potent ROS scavenging capacity. In murine sepsis models, Mn-CDs significantly improved systemic indices and were associated with macrophage anti-inflammatory states with enhanced efferocytosis, as evidenced by transcriptomic profiling. Integrated metagenomic/metabolomic analyses identified Mn-CDs-mediated enrichment of g_Clostridium and g_Bacteroides, concomitant with elevated indole-3-propionic acid (IPA) production. Subsequent in vitro studies demonstrate that IPA likely binds primarily to the aryl hydrocarbon receptor (AHR), promoting both efferocytosis and anti-inflammatory polarization in macrophages, thereby mitigating septic lung injury. Notably, the fecal microbiota transplantation (FMT) from Mn-CDs-treated mice not only alleviated systemic symptoms but also effectively promoted efferocytic polarization of pulmonary macrophages in septic mice. Depletion of the gut microbiota resulted in a significant loss of the protective efficacy of Mn-CDs in a murine model of septic lung injury. Collectively, the gut-lung axis mediated by microbiota-derived IPA and macrophage efferocytosis contributes to the remediation of septic lung injury, highlighting the potential of Mn-CDs in microbiome-directed critical care.
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来源期刊
ACS Nano
ACS Nano 工程技术-材料科学:综合
CiteScore
26.00
自引率
4.10%
发文量
1627
审稿时长
1.7 months
期刊介绍: ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.
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