ere fixed in 4% paraformaldehyde for 20 minutes and prepared for immunocytochemistry. Methods Pluripotent Cells and Culture Conditions hESCs and iPS lines were cultured on MEFs 345627-80-7 manufacturer plated at 1215,000 cells/cm2 in medium described previously. For daily feeding, 10 ng/ml FGF-2 was added or for stable FGF2 conditions, 7.5 microliters of FGF2 beads were added per 1 ml of growth media. Pluripotent cells grown without feeders were grown on Matrigel with either mTesR or MEF conditioned medium. Cells were passaged using 6 U/ml of dispase in hESC medium, washed and replated at a split of 1:5 to 1:10. Primary Neural Stem 21147071 Cell and Neural Progenitor Cell Culture NSCs and NPCs were isolated from the embryonic cortex as described previously. Cells were grown in adherent conditions on PLL or PLO coated plates in neural medium containing B27 and N2 and the presence of either 10 ng/ml FGF2 or FGF2 Beads. iPSC Generation Human fetal cornea fibroblasts from Advanced Bioscience Resource Inc., were used as starting material for iPSCs generated by transduction with four retroviral supernatants containing OCT4, SOX2, KLF4 and cMYC.The resulting iPSC lines were analyzed by immunostaining for expression of pluripotency markers, including OCT4, SOX2, Tra-1-60, Nanog, and SSEA4 SSEA1. 
Microsphere Preparation An aqueous solution containing human FGF2 in PBS, magnesium hydroxide in TE Buffer and Heparin were added to a Dichloromethane solution containing 200 mg of PLGA at a 1:1 ratio. The solution was vortexed and then polyvinylalcohol was added to produce a water/oil/water emulsion. It was then placed at 4 degrees overnight for DCM evaporation. The microspheres were then isolated by centrifugation and washed 3X with distilled water. FGF2 StemBeads purchased from StemCulture LLC brought about similar effects. Neural Induction Feeder-free hESC neural induction was carried out as previously described. Briefly, hESCs were plated at a density of 20,000 cells/cm2 on matrigel coated dishes in MEF conditioned hESC medium with 10 ng/mL of FGF-2 and10uM ROCK-inhibitor. The ROCK inhibitor was withdrawn, and hESCs were allowed to expand in CM for 3 days or until they were nearly confluent and then differentiated with 10 nM TGF-b inhibitor and 500 ng/mL of Noggin. Neural cells were removed with Accutase at day 11, 25,000 cells were plated in a 24 well plate. Quantitative Real-time PCR Total RNA was extracted using an RNeasy kit. For each sample, 1 mg of total RNA was treated for DNA contamination and reverse transcribed using Quantitect. Amplified material was detected using Taqman probes and PCR mix on a Mastercycler RealPlex2. All results were normalized to an HPRT control and are from 3 technical replicates of 3 independent biological samples at each data point. Western 16873882 Blot Samples were collected and proteins were harvested using RIPA buffer. 3 biological replicates were used for all time points. Protein was quantified using a BCA assay and 20 mgs of Sustained FGF2 Levels Better Maintain Stem Cells 7 Sustained FGF2 Levels Better Maintain Stem Cells differentiation potential was assessed for all three germ lineages. From left to right panels, hESCs grown using FGF2 beads gave rise to neural, mesodermal, and endodermal progeny, assessed by FACS for relevant markers. By qRT-PCR, FGF2 Beads expanded hESCs expressed higher levels of lineage markers after differentiation to all lineages. doi:10.1371/journal.pone.0056289.g003 protein were loaded in each well of a 412% Bis-Tris mini-g
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