Genetically Encoded Incorporation of IFN-α into Collagen-like Protein–Hyaluronic Acid Hydrogels for Diabetic Chronic Wound Healing
Source abstract
Abstract
The role of interferon-alpha is critical in modulating immune responses and the wound healing process. However, the rapid degradation and short lifespan of IFN-α in the body limit its therapeutic efficacy in wound management. This study presents an innovative approach to enhancing diabetic wound repair through the incorporation of IFN-α into double network hydrogels composed of hyaluronic acid and collagen-like protein (CLP). Two incorporation methods were evaluated: genetic fusion and spy-chemistry ligation. Our results demonstrate that IFN-α incorporated via spy-chemistry significantly outperformed genetic fusion in terms of cell viability, migration, and protein expression. In vivo studies further confirmed that spy-chemistry ligated IFN-α HA-CLP hydrogels markedly improved wound healing, as evidenced by elevated levels of COL-1α, CK-14, and α-SMA, compared to blank HA-CLP hydrogels and saline-treated controls. These findings underscore the potential of spy-chemistry ligated IFN-α-HA-CLP hydrogels as a promising therapeutic strategy for promoting effective wound healing in diabetic patients.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Wound Healing and Treatments · Diabetic Foot Ulcer Assessment and Management · Tendon Structure and Treatment
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Inner Mongolia Key Laboratory for Molecular Regulation of the Cell, School of Life Sciences, Inner Mongolia University, Hohhot 010051, People’s Republic of China
Funding
Department of Science and Technology of Inner Mongolia Autonomous Region · Natural Science Foundation of Inner Mongolia Autonomous Region · National Natural Science Foundation of China · Inner Mongolia Youth Science and Technology Talent Support Project
References (29)
Show source-provided references
1. 10.1038/s41590-020-0721-610.1038/s41590-020-0721-6 ↗
2. 10.1038/nbt136410.1038/nbt1364 ↗
3. 10.1126/science.abc206110.1126/science.abc2061 ↗
4. 10.1172/jci.insight.15276510.1172/jci.insight.152765 ↗
5. 10.1016/j.biomaterials.2019.11940310.1016/j.biomaterials.2019.119403 ↗
6. 10.1136/annrheumdis-2018-21319710.1136/annrheumdis-2018-213197 ↗
7. 10.3389/fimmu.2023.121632110.3389/fimmu.2023.1216321 ↗
8. 10.1016/j.jdiacomp.2022.10831710.1016/j.jdiacomp.2022.108317 ↗
9. 10.1016/j.ijbiomac.2019.08.23310.1016/j.ijbiomac.2019.08.233 ↗
10. 10.1016/j.cej.2022.13849410.1016/j.cej.2022.138494 ↗
11. 10.1016/j.actbio.2017.04.03410.1016/j.actbio.2017.04.034 ↗
12. 10.1016/j.biomaterials.2017.06.04310.1016/j.biomaterials.2017.06.043 ↗
13. 10.1016/j.jddst.2021.10289810.1016/j.jddst.2021.102898 ↗
14. 10.1016/j.biomaterials.2010.08.09810.1016/j.biomaterials.2010.08.098 ↗
15. 10.1002/adma.20210017610.1002/adma.202100176 ↗
16. 10.1002/adma.20140210510.1002/adma.201402105 ↗
17. 10.1002/adhm.20160079710.1002/adhm.201600797 ↗
18. 10.1002/adhm.20160013610.1002/adhm.201600136 ↗
19. 10.1002/adhm.20230382410.1002/adhm.202303824 ↗
20. 10.1039/D3BM01010D10.1039/D3BM01010D ↗
21. 10.1016/j.carbpol.2020.11712310.1016/j.carbpol.2020.117123 ↗
22. 10.1002/adfm.20210463010.1002/adfm.202104630 ↗
23. 10.1021/acsbiomaterials.1c0006910.1021/acsbiomaterials.1c00069 ↗
24. 10.1021/acsbiomaterials.1c0001810.1021/acsbiomaterials.1c00018 ↗
25. 10.1021/acsami.2c1993110.1021/acsami.2c19931 ↗
26. 10.1016/j.bioadv.2022.21315210.1016/j.bioadv.2022.213152 ↗
27. 10.3389/fimmu.2022.91822310.3389/fimmu.2022.918223 ↗
28. 10.1084/jem.2010110210.1084/jem.20101102 ↗
29. 10.1002/adfm.20200119610.1002/adfm.202001196 ↗