The central nervous system reserves high concentrations of free Zn(2+) in certain excitatory synaptic vesicles. In pathological conditions such as transient cerebral ischemia, traumatic brain injury, and kainic acid (KA)-induced seizure, free Zn(2+) is released in excess at synapses, which causes ne
Protective effect of autophagy in laser-induced glioma cell death in vitro
✍ Scribed by Aleksandar J. Krmpot; Kristina D. Janjetovic; Maja S. Misirkic; Ljubica M. Vucicevic; Dejan V. Pantelic; Darko M. Vasiljevic; Dusan M. Popadic; Branislav M. Jelenkovic; Vladimir S. Trajkovic
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 444 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0196-8092
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Background and Objective
Laser phototherapy could be potentially used for cancer treatment, but the mechanisms of laser‐induced cell death are not completely understood. Autophagy is the process in which the damaged cellular proteins and organelles are engulfed by and destroyed in acidified multiple‐membrane vesicles. The aim of the present study was to investigate the role of autophagy in laser‐induced tumor cell death in vitro.
Study Design/Materials and Methods
The monolayers of U251 human glioma tumor cells were exposed to 532 nm laser light from a single mode frequency‐doubled Nd‐YVO4 laser. A flattened Gaussian radial profile of laser beam (0.5–4 W) was used to uniformly illuminate entire colony of cells for various amounts of time (15–120 seconds) in the absence of cell culture medium. The cells were grown for 24 hours and the cell viability was determined by crystal violet or MTT assay. The presence of autophagy was assessed after 16 hours by fluorescence microscopy/flow cytometric analysis of acridine orange‐stained autophagolysosomes and Western blot analysis of the autophagosome‐associated LC3‐II protein. The concentration of the principal pro‐autophagic protein beclin‐1 was determined after 6 hours by cell‐based ELISA.
Results
The intracytoplasmic accumulation of autophagic vesicles, increase in LC3‐II and up‐regulation of beclin‐1 expression were clearly observed under irradiation conditions that caused approximately 50% cytotoxicity. Post‐irradiation addition of three different autophagy inhibitors (bafilomycin A1, chloroquine, or wortmannin) further increased the laser‐induced cytotoxicity, without affecting non‐irradiated cells.
Conclusions
These data indicate that beclin‐1‐dependent induction of autophagy can protect glioma cells from laser‐mediated cytotoxicity. Lasers Surg. Med. 42:338–347, 2010. © 2010 Wiley‐Liss, Inc.
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