Abstract
Tendon, a connective tissue structure, serves the crucial role of transmitting force between muscles and bones. However, tendon injury repair continues to pose a significant challenge in clinical settings. In this study, we utilized single-cell RNA sequencing to delve into the cell populations and signaling pathways that are integral to tendon healing. Our findings suggest that hypoxia plays a pivotal role in activating macrophages, stimulating endothelial cell migration, and fostering fibroblast proliferation. Based on these insights, we have developed a PCL scaffold coated with DFOA, which effectively mimics a hypoxic environment to enhance tendon tissue regeneration. Furthermore, the PCL-DFOA scaffolds exhibit exceptional ability in promoting macrophage polarization and angiogenesis. This research offers a therapeutic strategy that harnesses the regenerative power of hypoxia to accelerate and optimize tendon healing processes.
| Original language | English |
|---|---|
| Pages (from-to) | 8937-8948 |
| Number of pages | 12 |
| Journal | ACS Applied Materials and Interfaces |
| Volume | 17 |
| Issue number | 6 |
| DOIs | |
| State | Published - 12 Feb 2025 |
Keywords
- DFOA
- hypoxia
- macrophage
- single-cell RNA sequencing
- tendon regeneration