Recent advances to accelerate re-endothelialization for vascular stents
Open accessAbstract
Cardiovascular diseases are considered as one of the serious diseases that leads to the death of millions of people all over the world. Stent implantation has been approved as an easy and promising way to treat cardiovascular diseases. However, in-stent restenosis and thrombosis remain serious problems after stent implantation. It was demonstrated in a large body of previously published literature that endothelium impairment represents a major factor for restenosis. This discovery became the driving force for many studies trying to achieve an optimized methodology for accelerated re-endothelialization to prevent restenosis. Thus, in this review, we summarize the different methodologies opted to achieve re-endothelialization, such as, but not limited to, manipulation of surface chemistry and surface topography.
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Other agents including fucoidan, laminin, hyaluronic acid, chondroitin sulfate, type 1 collagen, and VEGF have been used to improve endothelialization on the surface of nano and metal stents and thin tissues such as heart valve and blood vessels.
“Other agents, including fucoidan (FU), laminin, hyaluronic acid (HA), chondroitin sulfate, type 1 collagen, and vascular endothelial growth factor (VEGF), have been used to improve endothelialization on the surface of nano and metal stents as well as thin tissues such as heart valve and blood vessels [231,234].”
From Liver tissue engineering using decellularized scaffolds: Current progress, challenges, and opportunities (2024) · cites this paper as [231]
The “Biomolecules for re-endothelialization” section (page not provided) names fucoidan, chondroitin sulfate, hyaluronic acid, laminin and collagen I as agents used to promote endothelial-cell growth. The “Surface chemistry on re-endothelialization” section also describes VEGF and fucoidan–laminin coatings on metallic substrates. The paper does not establish the claimed use of these agents on heart valves or other thin tissues, or specifically on nanostents. (LLM, conf=0.86)
Experimental — accuracy not yet measuredFibronectin is a major component present in decellularized tissues and has been extensively used for conjugation with biomaterial surfaces to accelerate attachment, spreading, and differentiation of ECs.
“Fibronectin, a large adhesive glycoprotein, is considered a major component present in decellularized tissues and has been extensively used for conjugation with biomaterial surfaces to accelerate the attachment, spreading, and differentiation of ECs [150,230,231].”
From Liver tissue engineering using decellularized scaffolds: Current progress, challenges, and opportunities (2024) · cites this paper as [231]
The “Biomolecules for re-endothelialization” section says fibronectin is a major ECM component and can be conjugated to biomaterial surfaces to promote EC attachment, spreading, and differentiation. It does not specifically identify fibronectin as a major component of decellularized tissues; the “Surface chemistry on re-endothelialization” section gives examples of its use on biomaterial surfaces. No page numbers are available in our copy. (LLM, conf=0.86)
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Estimation of nitric oxide production and reactionrates in tissue by use of a mathematical model
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Catalytic generation of nitric oxide from S-nitrosothiols using immobilized organoselenium species
Cha, W., & Meyerhoff, M. E. (2007) · Biomaterials · doi:10.1016/j.biomaterials.2006.08.019 · Cited by 140 · see citing works
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Cited by
Sorted by citations
Hussein, K. H., Park, K.-M., Yu, L., Song, S.-H., Woo, H.-M., & Kwak, H.-H. (2020) · Acta Biomaterialia · doi:10.1016/j.actbio.2019.12.029 · Cited by 44 · see citing works
Hussein, K. H., Ahmadzada, B., Correa, J. C., Sultan, A., Wilken, S., Amiot, B., & Nyberg, S. L. (2024) · Bioactive Materials · doi:10.1016/j.bioactmat.2024.06.001 · Cited by 28 · see citing works
“Fibronectin, a large adhesive glycoprotein, is considered a major component present in decellularized tissues and has been extensively used for conjugation with biomaterial surfaces to accelerate the attachment, spreading, and differentiation of ECs [150, 230,231].”
BackgroundMethod
- Authors
- Bedair, T. M., ElNaggar, M. A., Joung, Y. K., & Han, D. K.
- Affiliations
- Korea Institute of Science and Technology (KR)
- CHA University (KR)
- Corresponding author
- Han, Dong Keun
- Venue
- Journal of Tissue Engineering
- Publisher
- SAGE Publications
- Published
- 2017-01-01
- Volume
- 8
- Pages
- 2041731417731546-2041731417731546
- ISSN
- 2041-7314 (ISSN-L)
- PMC
- PMC5624345
- OpenAlex
- W2756579357
- Cited by
- 89
- References
- 2
- Citations by year
- 2026: 6 · 2025: 6 · 2024: 6 · 2023: 8 · 2022: 14 · 2021: 15 · 2020: 12 · 2019: 14 · 2018: 8
- FWCI
- 9.53
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Journal of Tissue Engineering (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Topics
- Health Sciences › Medicine › Surgery › Coronary Interventions and Diagnostics
- Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
- Physical Sciences › Materials Science › Surfaces, Coatings and Films › Polymer Surface Interaction Studies
- Keywords
- re-endothelialization, vascular stents, in-stent restenosis, stent thrombosis, surface chemistry, surface topography, stent surface modification
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