Lens epithelial cell response to polymer stiffness and polymer chemistry

Posterior capsule opacification (PCO) is the most common complication of cataract surgery, and intraocular lens (IOL) implantation is the standard of care for cataract patients. Induction of postoperative epithelial‐mesenchymal transition (EMT) in residual lens epithelial cells (LEC) is the main mec...

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Veröffentlicht in:Journal of polymer science (2020) 2024-05, Vol.62 (9), p.1820-1830
Hauptverfasser: Hamedi, Hamid, Green, Spencer W., Puri, Raima, Luo, Richard, Lee, Michael, Liu, Jian, Cho, Hanna, Hansford, Derek J., Chandler, Heather L., Swindle‐Reilly, Katelyn E.
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Sprache:eng
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Zusammenfassung:Posterior capsule opacification (PCO) is the most common complication of cataract surgery, and intraocular lens (IOL) implantation is the standard of care for cataract patients. Induction of postoperative epithelial‐mesenchymal transition (EMT) in residual lens epithelial cells (LEC) is the main mechanism by which PCO forms. Previous studies have shown that IOLs made with different materials have varying incidence of PCO. The aim of this paper was to study the interactions between human (h)LEC and polymer substrates. Polymers and copolymers of 2‐hydroxyethyl methacrylate (HEMA) and 3‐methacryloxypropyl tris(trimethylsiloxy)silane (TRIS) were synthesized and evaluated due to the clinical use of these materials as ocular biomaterials and implants. The chemical properties of the polymer surfaces were evaluated by contact angle, and polymer stiffness and roughness were measured using atomic force microscopy. In vitro studies showed the effect of polymer mechanical properties on the behavior of hLECs. Stiffer polymers increased α‐smooth muscle actin expression and induced cell elongation. Hydrophobic and rough polymer surfaces increased cell attachment. These results demonstrate that attachment of hLECs on different surfaces is affected by surface properties in vitro, and evaluating these properties may be useful for investigating prevention of PCO.
ISSN:2642-4150
2642-4169
2642-4169
DOI:10.1002/pol.20230736