AI Article Synopsis

  • Zinc and its alloys show promise as biodegradable metals for vascular stents, but more research is needed on how they interact with surrounding cells.
  • A study investigated the effects of zinc on three types of human vascular cells, finding differing levels of cytotoxicity with human dermal fibroblasts being the most sensitive.
  • By modifying the zinc surface with gelatin, which mimics a natural protein layer, cells were able to attach and grow, indicating that free zinc may inhibit cell adhesion and movement.

Article Abstract

Zinc (Zn) and its alloys have recently been introduced as a new class of biodegradable metals with potential application in biodegradable vascular stents. Although an in vivo feasibility study pointed to outstanding biocompatibility of Zn-based implants in vascular environments, a thorough understanding of how Zn and Zn affect surrounding cells is lacking. In this comparative study, three vascular cell types-human endothelial cells (HAEC), human aortic smooth muscle cells (AoSMC), and human dermal fibroblasts (hDF)-were studied to advance the understanding of Zn/Zn-cell interactions. Aqueous cytotoxicity using a Zn insult assay resulted in LD values of 50 µM for hDF, 70 µM for AoSMC, and 265 µM for HAEC. Direct cell contact with the metallic Zn surface resulted initially in cell attachment, but was quickly followed by cell death. After modification of the Zn surface using a layer of gelatin-intended to mimic a protein layer seen in vivo-the cells were able to attach and proliferate on the Zn surface. Further experiments demonstrated a Zn dose-dependent effect on cell spreading and migration, suggesting that both adhesion and cell mobility may be hindered by free Zn.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5102339PMC
http://dx.doi.org/10.1021/acsbiomaterials.6b00035DOI Listing

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