红细胞生成
氧化应激
再生障碍性贫血
造血
促红细胞生成素
无效红细胞生成
贫血
活性氧
细胞凋亡
癌症研究
免疫学
医学
药理学
干细胞
化学
生物
细胞生物学
生物化学
骨髓
内科学
作者
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,Yongqiang Li
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-01-07
标识
DOI:10.1021/acsnano.4c16766
摘要
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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