Degraded products generated by iron stent inhibit the vascular smooth muscle cell proliferation by downregulating AP-1.

ABSTRACT: In-stent restenosis (ISR) following interventional therapy is a fatal clinical complication. Current evidence indicates that neointimal hyperplasia driven by uncontrolled proliferation of vascular smooth muscle cells (VSMC) is a major cause of restenosis. This implies that inhibiting VSMC proliferation may be an attractive approach for preventing in-stent restenosis. In our previous study, we found that the iron stent reduced the neointimal hyperplasia in an atherosclerotic artery stenosis model, and the iron corroded granules generated by the iron stent inhibited neointimal hyperplasia by suppressing the proliferation of VSMCs. However, this observation needs to be validated through in vitro experimentation. In this study, co-culture experiments and flow cytometer assays were performed to

SUBMITTER: Huang J 

PROVIDER: S-EPMC11725540 | biostudies-literature | 2025 Jan

REPOSITORIES: biostudies-literature