journal article·2025-01-21

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

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

ACS Nano· Volume 19· Issue 2
Publisher page

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.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Carbon and Quantum Dots Applications · Neonatal Health and Biochemistry · Erythrocyte Function and Pathophysiology

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Institute of Advanced Interdisciplinary Science, School of Physics, Shandong University, Jinan 250100, China

Department of Orthopedics, Tianjin Medical University General Hospital, Tianjin 300070, China

Gastroenterology ICU, Department of Gastroenterology, Qilu Hospital of Shandong University, Jinan 250012, China

Laboratory Animal Center of Shandong University, Jinan 250012, China

Orthopedic Department, 960 Hospital of People’s Liberation Army, Jinan 250031, China

Funding

National Key Research and Development Program of China · Taishan Scholar Project of Shandong Province · Cyrus Tang Foundation · National Natural Science Foundation of China · Natural Science Foundation of Shandong Province

References (47)

Show source-provided references
1. 10.1016/S0140-6736(05)66515-410.1016/S0140-6736(05)66515-4 ↗
2. 10.1111/bjh.1385310.1111/bjh.13853 ↗
3. 10.1056/NEJMra141348510.1056/NEJMra1413485 ↗
4. 10.1182/blood-2016-08-69348110.1182/blood-2016-08-693481 ↗
5. 10.1016/j.jpeds.2008.06.00410.1016/j.jpeds.2008.06.004 ↗
6. 10.1007/s10741-008-9083-010.1007/s10741-008-9083-0 ↗
7. 10.1186/s13045-018-0564-x10.1186/s13045-018-0564-x ↗
8. 10.3324/haematol.1285510.3324/haematol.12855 ↗
9. 10.1182/blood-2006-03-01077710.1182/blood-2006-03-010777 ↗
10. 10.1182/blood.201900094010.1182/blood.2019000940 ↗
11. 10.1053/j.seminhematol.2021.12.00210.1053/j.seminhematol.2021.12.002 ↗
12. 10.7150/thno.4679410.7150/thno.46794 ↗
13. 10.1021/acsnano.8b0932710.1021/acsnano.8b09327 ↗
14. 10.1016/j.nantod.2023.10196510.1016/j.nantod.2023.101965 ↗
15. 10.3892/mmr.2020.1165310.3892/mmr.2020.11653 ↗
16. 10.1016/j.yexcr.2023.11360310.1016/j.yexcr.2023.113603 ↗
17. 10.19540/j.cnki.cjcmm.20200304.10110.19540/j.cnki.cjcmm.20200304.101 ↗
18. 10.5582/ddt.2014.0103810.5582/ddt.2014.01038 ↗
19. 10.1016/j.jep.2014.02.01210.1016/j.jep.2014.02.012 ↗
20. 10.1007/s40820-018-0223-310.1007/s40820-018-0223-3 ↗
21. 10.34133/research.015210.34133/research.0152 ↗
22. 10.1021/acsnano.3c1220110.1021/acsnano.3c12201 ↗
23. 10.1002/adma.20220090510.1002/adma.202200905 ↗
24. 10.1038/s41467-023-35828-210.1038/s41467-023-35828-2 ↗
25. 10.1002/adfm.20221385610.1002/adfm.202213856 ↗
26. 10.1002/eem2.1203810.1002/eem2.12038 ↗
27. 10.1002/smll.20190264110.1002/smll.201902641 ↗
28. 10.1021/acsnano.2c0161910.1021/acsnano.2c01619 ↗
29. 10.1142/S0192415X0700532610.1142/S0192415X07005326 ↗
30. 10.1016/j.jep.2016.02.01910.1016/j.jep.2016.02.019 ↗
31. Fu Y. · Chin. Trad. Pat. Med. · 2023 · 45 · 2250
32. 10.1016/j.blre.2012.12.00310.1016/j.blre.2012.12.003 ↗
33. 10.1159/00048843610.1159/000488436 ↗
34. 10.1016/j.cell.2004.08.01410.1016/j.cell.2004.08.014 ↗
35. 10.1016/j.freeradbiomed.2018.04.57810.1016/j.freeradbiomed.2018.04.578 ↗
36. 10.1073/pnas.090929610610.1073/pnas.0909296106 ↗
37. 10.1016/j.celrep.2016.06.08510.1016/j.celrep.2016.06.085 ↗
38. 10.1002/iub.219210.1002/iub.2192 ↗
39. 10.1016/j.carbon.2023.01.00610.1016/j.carbon.2023.01.006 ↗
40. 10.1016/j.freeradbiomed.2004.07.00210.1016/j.freeradbiomed.2004.07.002 ↗
41. 10.1016/j.ejcb.2017.11.00310.1016/j.ejcb.2017.11.003 ↗
42. 10.1007/s11010-016-2811-110.1007/s11010-016-2811-1 ↗
43. 10.1038/nm.381410.1038/nm.3814 ↗
44. 10.1016/j.bone.2018.03.01410.1016/j.bone.2018.03.014 ↗
45. 10.1182/blood-2013-01-47639010.1182/blood-2013-01-476390 ↗
46. 10.1002/advs.20210525210.1002/advs.202105252 ↗
47. 10.34133/2022/976764310.34133/2022/9767643 ↗