Alysis of brain tissue reveals that stress-resistant cells in vitro showed similar features to the less vulnerable cerebellum in mice, whereas stress-sensitive cells resembled the highly sensitive hippocampal area [42]. These results highlight the possibility that alterations in membraneLysosomal Stability Is Regulated by CholesterolFigure 5. Cholesterol Accumulation Protects MEFs from Oxidative Stress-induced Apoptosis, Independent of the Expression of LAMP Proteins. A) Localization (scale bar 10 mm) and B) expression of lysosome-associated membrane protein-2 (LAMP-2) in wt and NPC1-mutant (NPC1mut) human fibroblasts. Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was used to verify equal protein loading. One representative blot out of three is shown. C) Phase contrast images (scale bar 5 mm) and D) viability analysis (n = 4) of wt mouse embryonic order CI 1011 fibroblasts (MEFs) and MEFs deficient for LAMP-1 (LAMP-12/2) or LAMP-2 (LAMP-22/2) 24 h after H2O2 exposure, with or without U18666A pretreatment. Viability was measured by crystal violet staining and expressed as percentage of untreated cultures. Data are presented as the mean 6 SD, * p#0.05) Filipin staining in MEFs, with or without U18666A treatment. Scale bar 10 mm. doi:10.1371/journal.pone.0050262.gcholesterol composition may be at least partly involved in the responses allowing neurons to cope with prolonged stress. Several factors have been suggested to be involved in the regulation of lysosomal stability, such as the lipid composition of the lysosomal membrane as well as lysosomal membrane proteins. Our results demonstrate that the manipulation of lysosomal cholesterol content can be used to modify apoptosis sensitivity. Our data indicate that short-term lysosomal cholesterol modulation might be used as a therapeutic strategy for conditions associated with accelerated or repressed apoptosis.Cells and culture conditionsWt (GM05659) and NPC1-mutant (GM18436) human fibroblasts (passages 12?4; Coriell Institute, Camden, NJ, USA) were cultured in Eagle’s minimum essential medium supplemented with 10 fetal calf serum, 2 mM glutamine, 50 IU/ml penicillin-G and 50 mg/ml streptomycin (all from Gibco, Paisley, UK). Cells were incubated in humidified air with 5 CO2 at 37uC and were Peptide M chemical information subcultured once a week. Primary cultures of newborn rat neurons were obtained essentially as described 
elsewhere [43]. In short, newborn Sprauge-Dawley rats (Taconic Europe, Lilla Skensved, Denmark) were decapitated and the cortex dissected. The cortex tissue was sieved through a nylon mesh (80 mm) into 
Neurobasal A medium, 50 IU/ml penicillin, 50 mg/ml streptomycin, 0.5 mM glutamine and 2 B27 supplement, with addition of 5 ng/ml bfibroblast growth factor (b-FGF; b-fibroblast growth factor Life Technologies, Darmstadt, Germany). Cells were plated on poly-Llysine coated surface at a density of 100000 cells/cm2. After 24 h, 1326631 half of the media was changed to receive a final concentration of 10 ng/ml b-FGF. Every third day, half of the medium wasMaterials and Methods Ethics statementThe animal experiments were approved by the Ethics Committee for Animal Research at Linkoping University (permit ?number 101/08).Lysosomal Stability Is Regulated by CholesterolFigure 6. Cholesterol Modulation Influences the Sensitivity of MEFs to Oxidative Stress-induced Apoptosis. Mouse embryonic fibroblasts (MEFs) deficient for both LAMP-1 and LAMP-2 (LAMPnull) were treated with U18666A or methyl-b-cyclodextrin (MbCD). A) Filipin staini.Alysis of brain tissue reveals that stress-resistant cells in vitro showed similar features to the less vulnerable cerebellum in mice, whereas stress-sensitive cells resembled the highly sensitive hippocampal area [42]. These results highlight the possibility that alterations in membraneLysosomal Stability Is Regulated by CholesterolFigure 5. Cholesterol Accumulation Protects MEFs from Oxidative Stress-induced Apoptosis, Independent of the Expression of LAMP Proteins. A) Localization (scale bar 10 mm) and B) expression of lysosome-associated membrane protein-2 (LAMP-2) in wt and NPC1-mutant (NPC1mut) human fibroblasts. Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was used to verify equal protein loading. One representative blot out of three is shown. C) Phase contrast images (scale bar 5 mm) and D) viability analysis (n = 4) of wt mouse embryonic fibroblasts (MEFs) and MEFs deficient for LAMP-1 (LAMP-12/2) or LAMP-2 (LAMP-22/2) 24 h after H2O2 exposure, with or without U18666A pretreatment. Viability was measured by crystal violet staining and expressed as percentage of untreated cultures. Data are presented as the mean 6 SD, * p#0.05) Filipin staining in MEFs, with or without U18666A treatment. Scale bar 10 mm. doi:10.1371/journal.pone.0050262.gcholesterol composition may be at least partly involved in the responses allowing neurons to cope with prolonged stress. Several factors have been suggested to be involved in the regulation of lysosomal stability, such as the lipid composition of the lysosomal membrane as well as lysosomal membrane proteins. Our results demonstrate that the manipulation of lysosomal cholesterol content can be used to modify apoptosis sensitivity. Our data indicate that short-term lysosomal cholesterol modulation might be used as a therapeutic strategy for conditions associated with accelerated or repressed apoptosis.Cells and culture conditionsWt (GM05659) and NPC1-mutant (GM18436) human fibroblasts (passages 12?4; Coriell Institute, Camden, NJ, USA) were cultured in Eagle’s minimum essential medium supplemented with 10 fetal calf serum, 2 mM glutamine, 50 IU/ml penicillin-G and 50 mg/ml streptomycin (all from Gibco, Paisley, UK). Cells were incubated in humidified air with 5 CO2 at 37uC and were subcultured once a week. Primary cultures of newborn rat neurons were obtained essentially as described elsewhere [43]. In short, newborn Sprauge-Dawley rats (Taconic Europe, Lilla Skensved, Denmark) were decapitated and the cortex dissected. The cortex tissue was sieved through a nylon mesh (80 mm) into Neurobasal A medium, 50 IU/ml penicillin, 50 mg/ml streptomycin, 0.5 mM glutamine and 2 B27 supplement, with addition of 5 ng/ml bfibroblast growth factor (b-FGF; b-fibroblast growth factor Life Technologies, Darmstadt, Germany). Cells were plated on poly-Llysine coated surface at a density of 100000 cells/cm2. After 24 h, 1326631 half of the media was changed to receive a final concentration of 10 ng/ml b-FGF. Every third day, half of the medium wasMaterials and Methods Ethics statementThe animal experiments were approved by the Ethics Committee for Animal Research at Linkoping University (permit ?number 101/08).Lysosomal Stability Is Regulated by CholesterolFigure 6. Cholesterol Modulation Influences the Sensitivity of MEFs to Oxidative Stress-induced Apoptosis. Mouse embryonic fibroblasts (MEFs) deficient for both LAMP-1 and LAMP-2 (LAMPnull) were treated with U18666A or methyl-b-cyclodextrin (MbCD). A) Filipin staini.
