m 7900HT Detection System. Cycling conditions started at 50 C for 2 min, followed by 95uC for 10 min, then 40 cycles of 95uC for 15 sec and 60uC for 1 min. The cycle threshold was placed at a set level where the exponential increase in PCR amplification was approximately parallel between all samples. Relative fold change was calculated by comparing Ct values between the target gene and GAPDH as the reference guide. The DDCt method was used to analyze the relative changes in gene expression. 5-aza-29-deoxycytidine treatment Monolayer cultures at approximately 40% confluence were starved in serum-free medium overnight and treated with vehicle or 0.5, 1, 3, 5, 10, 15, or 20 mM of the DNMT inhibitor 5-azadC for 5 days. The medium was changed every 24 hrs. Total RNA was isolated using Tri-reagent. All of the experiments were repeated in triplicate using samples from at least 7 new different subjects not previously used in microarrays, 4 subjects were ” African- and 3 Caucasian-American. Real-time quantitative RT-PCR Total RNA from fresh tissues and leiomyoma smooth muscle cells was MedChemExpress DHMEQ extracted using Tri-reagent and the RNeasy Fibrous Tissue kit. cDNA was prepared with Protein Analysis Protein was extracted from 50 mg of frozen tissues using mammalian protein extraction reagent. Genome-Wide DNA Methylation in Uterine Leiomyoma Lysates were cleared by centrifugation at 14, 000 rpm for 10 min. Equal amounts of protein were resolved on 412% Ready Gel Precast Gels, and transferred onto PVDF membranes. The membranes were bloted with antihuman KLF11 antibodies 1:1000, DLEC1 1:500, and KRT19 1:1000. Anti-GAPDH antibody was used as a loading control. Dectection was detected using a Supersignal West Femto. Quantification of the immunoblots was done using ImageJ software and normalized to GAPDH. Statistical analysis Statistical significance was determined by Student’s t test and one-way ANOVA followed by Fisher’s protected least significant difference test. Significance was accepted at P,0.05. Characteristic features of early AMD include the accumulation of subretinal deposits between RPE and Bruch’s membrane and RPE morphologic changes. Dysregulated growth factor expression, scavenger receptors, and the mTOR pathway have all been implicated in mediating or modulating these pathologic changes. Redox of RPE also plays a critical role in combating oxidative stress. Among the cellular antioxidant constituents, reduced glutathione is the major non-protein thiol antioxidant with pluripotent functions. Even though GSH is synthesized in the cytosol, it is distributed in intracellular organelles such as endoplasmic reticulum, nucleus and mitochondria. GSH depletion has been attributed to apoptosis either by predisposing cells to apoptosis or by modulating mitochondrial membrane potential and 
9528756 subsequent activation of caspases. Since mitochondrial GSH plays a significant role in cellular defense against pro-oxidants, depletion of mGSH poses a threat to cell viability. Elucidating GSH transport mechanisms of different cellular compartments has received considerable recent attention. In the brain, release of GSH from astrocytes is an important component of GSH homeostasis. Brain astrocytes maintain redox balance by the ATP-dependent extrusion of GSH by ATP-binding cassette transporter, multidrug resistance protein 1 . Studies have demonstrated that both glutathione disulfide and GSH are substrates for MRP1. However, information on expression and regulation of protein