The Effect of Photodynamic Therapy with Bacteriochlorin a on Lens Epithelial Cells in a Capsular Bag Model

• Published in: Experimental eye research 2001-01, Vol.72 (1), p.41-48
• Main Authors: van Tenten, Yasmine, Schuitmaker, Hans J., De Wolf, Anneke, Willekens, Ben, Vrensen, Gijs F.J.M., Tassignon, Marie-José
• Format: Article
• Language: English
• Subjects: Adult; Aged; apoptosis; Apoptosis - drug effects; Bacteriochlorophylls - therapeutic use; Biological and medical sciences; capsular bag model; Cataract - drug therapy; Cataract Extraction; Cell Division - drug effects; Epithelial Cells - drug effects; Eye; histology; Humans; Lens Capsule, Crystalline - cytology; Lens Capsule, Crystalline - drug effects; Medical sciences; Middle Aged; Pharmacology. Drug treatments; Photochemotherapy; photodynamic therapy; Photosensitizing Agents - therapeutic use; Porphyrins - therapeutic use; posterior capsule opacification; Postoperative Complications - drug therapy
• ISSN: 0014-4835; 1096-0007
• DOI: 10.1006/exer.2000.0924

Photodynamic therapy (PDT) with bacteriochlorin a(BCA) has proved to be a successful treatment for many cancers and to be cytocidal for different cell lines in culture. The present study aimed to investigate in vitro the potential of this treatment for killing lens epithelial cells (LECs) left in the human capsular bag after extracapsular cataract extraction (ECCE). Capsular bags were prepared from donor eyes using an ECCE procedure and incubated in various concentrations of bacteriochlorin a(1.6–50μ gml−1) during various incubation periods (2–10min). Subsequently, the capsules were illuminated during various exposure times (2–15min) with a diode laser (wavelength 760nm). After treatment, the capsular bags were cultured for 7 days in Eagle’s minimal essential medium supplemented with 2% fetal calf serum. The specimens were fixed in glutaraldehyde/paraformaldehyde and examined with routine light microscopy, Hoechst staining for DNA and transmission electron microscopy. Proliferation of LECs on the posterior capsule was assessed in flat mounts. Capsular bags receiving BCA without illumination and capsular bags receiving illumination only served as controls. BCA alone or light alone have no effect on structure and proliferative activity of LECs. At a threshold protocol of incubation in BCA at 10μ gml−1for 10min and subsequent illumination for 15min, proliferative activity of cells is largely arrested and nearly all LECs on the capsule exhibit severe signs of apoptosis. Photodynamic therapy with bacteriochlorin a induces cell death and suppression of proliferation inlens epithelial cells and could be a promising means of prevention of posterior capsule opacification.