Donkey-Hide Gelatin-Derived Carbon Dots Activate Erythropoiesis and Eliminate Oxidative Stress for Aplastic Anemia Treatment

IF 15.8 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY ACS Nano Pub Date : 2025-01-07 DOI:10.1021/acsnano.4c16766
Chunzhen Wang, Jinghui Li, Kehan Liu, Junjin Li, Fan Zhang, Xiaomin Ma, Yuezheng Li, Chengmei Zhang, Xiangdong Liu, Yuanyuan Qu, Mingwen Zhao, Weifeng Li, Weimin Huang, Yong-Qiang Li
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Abstract

Aplastic anemia (AA) is a life-threatening hematologic disease with limited therapeutic options. Stalled erythropoiesis and oxidative stress-induced hemocyte apoptosis are the main pathological features of AA, yet therapeutic agents that address these issues remain elusive. In this study, we report distinctive donkey-hide gelatin-derived carbon dots (G-CDs) that enable erythropoiesis activation and oxidative stress elimination to tackle refractory AA. We demonstrate that G-CDs can promote the proliferation and erythroid differentiation of hematopoietic stem cells as well as erythrocyte maturation, activating the whole process of erythropoiesis. Moreover, G-CDs display multienzyme-like activities and dramatically alleviate the oxidative stress of bone marrow and peripheral blood via catalytic scavenging of multiple reactive oxygen species, reconstructing the hematopoietic microenvironment. Intravenously or orally administered to AA mice induced by chemotherapy drugs, G-CDs significantly boost the level of red blood cells and hemoglobin and lead to the complete recovery of hematopoietic function, showing better therapeutic performance than clinically approved erythropoietin (EPO) without adverse effects. By collaboratively addressing the issues of stalled erythropoiesis and oxidative stress, the G-CDs-based intervention strategy may offer a powerful paradigm for clinical AA management.

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驴皮明胶碳点活化红细胞和消除氧化应激治疗再生障碍性贫血
再生障碍性贫血(AA)是一种危及生命的血液病,治疗选择有限。红细胞生成停滞和氧化应激诱导的血细胞凋亡是AA的主要病理特征,但解决这些问题的治疗药物仍然难以捉摸。在这项研究中,我们报道了独特的驴皮明胶衍生碳点(G-CDs),它能够激活红细胞生成和消除氧化应激,以解决难治性AA。我们发现G-CDs可以促进造血干细胞的增殖和红细胞分化,促进红细胞成熟,激活整个红细胞生成过程。此外,G-CDs表现出多酶样活性,通过催化清除多种活性氧,显著缓解骨髓和外周血的氧化应激,重建造血微环境。G-CDs静脉或口服化疗药物诱导的AA小鼠,可显著提高红细胞和血红蛋白水平,使造血功能完全恢复,治疗效果优于临床批准的促红细胞生成素(EPO),且无不良反应。通过协作解决红细胞生成停滞和氧化应激问题,基于g - cds的干预策略可能为临床AA管理提供强有力的范例。
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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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