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Comparison of Gelatin/Polylysine‐ and Silk Fibroin/SDF‐1α‐Coated Mesenchymal Stem Cell‐Seeded Intracranial Stents

Endothelialization of the aneurysmal neck is essential for aneurysm healing after endovascular treatment. Mesenchymal stem cell (MSC)‐seeded stents can promote aneurysm repair. The biological effects of coated and uncoated nitinol intracranial stents seeded with MSCs on vascular cells and macrophage...

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Published in:Macromolecular bioscience 2023-04, Vol.23 (4), p.e2200402-n/a
Main Authors: Peng, Qichen, Guo, Ruimin, Zhou, Yangyang, Teng, Ruidi, Cao, Yulin, Mu, Shiqing
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cited_by cdi_FETCH-LOGICAL-c3732-89da71fdaea4d5b4d823cf57de28ef437a763a48d609ce35afc43b189abe7b273
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description Endothelialization of the aneurysmal neck is essential for aneurysm healing after endovascular treatment. Mesenchymal stem cell (MSC)‐seeded stents can promote aneurysm repair. The biological effects of coated and uncoated nitinol intracranial stents seeded with MSCs on vascular cells and macrophage proliferation and inflammation are investigated. Two stent coatings that exert pro‐aggregation effects on MSCs via different mechanisms are examined: gelatin/polylysine (G/PLL), which enhances cell adhesion, and silk fibroin/SDF‐1α (SF/SDF‐1α), which enhances chemotaxis. The aim is to explore the feasibility of MSC‐seeded coated stents in the treatment of intracranial aneurysms. The G/PLL coating provides the highest cytocompatibility and blood compatibility substrate for MSCs and vascular cells and promotes cell adhesion and proliferation. Moreover, it enhances MSC secretion and regulation of vascular cell and macrophage proliferation and chemotaxis. Although the SF/SDF‐1α coating promotes MSC secretion and vascular cell chemotaxis, it induces a greater degree of macrophage proliferation, chemotaxis, and secretion of pro‐inflammatory factors. MSC‐seeded stents coated with G/PLL may benefit stent surface endothelialization and reduce the inflammatory response after endovascular treatment of intracranial aneurysm. These effects may improve aneurysm healing and increase the cure rate. A stent that is capable of inducing rapid surface endothelialization may promote aneurysm healing. Two stent coatings that exert pro‐aggregation effects on MSCs via different mechanisms are examined in vitro: gelatin/polylysine (G/PLL), which enhances cell adhesion, and silk fibroin/SDF‐1α (SF/SDF‐1α), which enhances chemotaxis. MSC‐seeded stents coated with G/PLL may benefit stent surface endothelialization and reduce the inflammatory response after endovascular treatment of intracranial aneurysm.
doi_str_mv 10.1002/mabi.202200402
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Although the SF/SDF‐1α coating promotes MSC secretion and vascular cell chemotaxis, it induces a greater degree of macrophage proliferation, chemotaxis, and secretion of pro‐inflammatory factors. MSC‐seeded stents coated with G/PLL may benefit stent surface endothelialization and reduce the inflammatory response after endovascular treatment of intracranial aneurysm. These effects may improve aneurysm healing and increase the cure rate. A stent that is capable of inducing rapid surface endothelialization may promote aneurysm healing. Two stent coatings that exert pro‐aggregation effects on MSCs via different mechanisms are examined in vitro: gelatin/polylysine (G/PLL), which enhances cell adhesion, and silk fibroin/SDF‐1α (SF/SDF‐1α), which enhances chemotaxis. 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source Wiley-Blackwell Read & Publish Collection
subjects Adhesion
Aneurysm
Aneurysms
bioactive coatings
Biocompatibility
Biological effects
Cardiovascular system
Cell adhesion
Cell adhesion & migration
Cell proliferation
Chemokine CXCL12 - pharmacology
Chemotaxis
Coatings
Fibroins - pharmacology
Gelatin
Gelatin - pharmacology
Healing
Humans
Implants
Inflammation
Inflammatory response
Intracranial Aneurysm - therapy
intracranial stents
Macrophages
Mesenchymal Stem Cells
Nickel titanides
Polylysine
Polylysine - pharmacology
Secretion
Silk
Silk fibroin
Stem cells
Stents
Substrates
surface modifications
title Comparison of Gelatin/Polylysine‐ and Silk Fibroin/SDF‐1α‐Coated Mesenchymal Stem Cell‐Seeded Intracranial Stents
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