S were markedly increased with NCMs co-culture, compared with EKs Licochalcone-A site co-culture (n = 5). The percentage of positive staining was calculated on the basis of the total number of cells in each view. B, Cell apoptosis assay by flow cytometry using Annexin V-FITC apoptosis assay kit at late-stage differentiation. C, Statistical analysis on flow cytometry results 25033180 shows that there was no baseline difference in cell apoptosis in each group (n = 5). Scale bars = 100 mm. doi:10.1371/journal.pone.0055233.gAn Indirect Co-Culture Model for ESCsstepwise analysis on ESC differentiation and mimicking endogenous signals from NCMs are the most likely to increase and maintain the efficiencies of ESCs as well as other pluripotent stem cells differentiation into CM lineages.Indirect Co-culture ModelThe 100 mm uncoated Petri dishes (Greiner Bio-One, Monroe, NC) were used to form EBs. After pipetting the 20 mL drops (400 cells) onto lids, lids were placed back on the 100 mm dish containing 10 mL PBS to prevent drying out of hanging drops. Each time there were 200 EBs formed in a 100 mm dish. On Day 3 of hanging drop culture, the cell aggregates were purchase Licochalcone A transferred and cultured in suspension in cell culture flasks (BD Bioscience) with differentiation medium for additional 2 days. 5-day-old EBs were carefully transferred to the 6- or 12-well plates coated with 0.2 gelatin and continuously cultured in differentiation medium. The medium for differentiation was above-mentioned ESC culture medium without LIF, but 0.1 mmol/L ascorbic acid (Sigma) was added to induce CM differentiation [6]. As previously described by Maltsev et al. [3], early-stage differentiation (shortly after the initiation of contractions) was day (8+3), intermediate-stage differentiation was day (8+8), and late-stage differentiation was day (8+16). The MillicellTM hanging cell culture inserts (PET membranes with 1 mm pores) (Millipore, Bedford, MA, USA) can be especially used for co-culture. Two cell populations that are co-cultured in different compartments (insert and well) stay physically separated, but may communicate via paracrine signaling through the pores of the membrane. Here, 5-day-old EBs were transferred to 6- or 12well plate coated with 0.2 gelatin, then the inserts were placed in some well of 6- or 12- well plate followed by EKs or the NCMs seeding on the inserts. Culture medium was the mentioned differentiation medium and changed every day. The PET membrane with 1 mm pores will become translucence in the presence of water, so we can observe the cells in the upper chamber or on bottom through a microscope. Spontaneously contracting cells appeared as clusters in outgrowths from the EBs. With daily gentle media changes and low 
EB density, the EBs continued to contract in culture for a period of observation of up to 36 days.Materials and Methods Generation of aMHC-GFP Transgenic MiceTo generate aMHC-GFP transgenic mice, eGFP-Rex-Neomycin cDNA was sucloned into the expression vector containing amyosin heavy chain promoter [29]. This Plasmid (aMHC-eGFPRex-Neo, No. 21229) was obtained from Addgene. Pronuclear microinjection and other procedures were performed by Cyagen Biosciences according to the standard protocols. Genotyping was performed by PCR on tail DNA with the following primer: eGFP forward: 59-ACGTAAACGGCCACAAGTTC-39; eGFP backward: 59- GATCTTGAAGTTCACCTTGATGC-39.Cell Culture of ESCsMouse CGR8 ESCs, previously established from strain 129P2/ Ola mouse embryos by Smith et al. [30], w.S were markedly increased with NCMs co-culture, compared with EKs co-culture (n = 5). The percentage of positive staining was calculated on the basis of the total number of cells in each view. B, Cell apoptosis assay by flow cytometry using Annexin V-FITC apoptosis assay kit at late-stage differentiation. C, Statistical analysis on flow cytometry results 25033180 shows that there was no baseline difference in cell apoptosis in each group (n = 5). Scale bars = 100 mm. doi:10.1371/journal.pone.0055233.gAn Indirect Co-Culture Model for ESCsstepwise analysis on ESC differentiation and mimicking endogenous signals from NCMs are the most likely to increase and maintain the efficiencies of ESCs as well as other pluripotent stem cells differentiation into CM lineages.Indirect Co-culture ModelThe 100 mm uncoated Petri dishes (Greiner Bio-One, Monroe, NC) were used to form EBs. After pipetting the 20 mL drops (400 cells) onto lids, lids were placed back on the 100 mm dish containing 10 mL PBS to prevent drying out of hanging drops. Each time there were 200 EBs formed in a 100 mm dish. On Day 3 of hanging drop culture, the cell aggregates were transferred and cultured in suspension in cell culture flasks (BD Bioscience) with differentiation medium for additional 2 days. 5-day-old EBs were carefully transferred to the 6- or 12-well plates coated with 0.2 gelatin and continuously cultured in differentiation medium. The medium for differentiation was above-mentioned ESC culture medium without LIF, but 0.1 mmol/L ascorbic acid (Sigma) was added to induce CM differentiation [6]. As previously described by Maltsev et al. [3], early-stage differentiation (shortly after the initiation of contractions) was day (8+3), intermediate-stage differentiation was day (8+8), and late-stage differentiation was day (8+16). The MillicellTM hanging cell culture inserts (PET membranes with 1 mm pores) (Millipore, Bedford, MA, USA) can be especially used for co-culture. Two cell populations that are co-cultured in different compartments (insert and well) stay physically separated, but may communicate via paracrine signaling through the pores of the membrane. Here, 5-day-old EBs were transferred to 6- or 12well plate coated with 0.2 gelatin, then the inserts were placed in some well of 6- or 12- well plate followed by EKs or the NCMs seeding on the inserts. Culture medium was the mentioned differentiation medium and changed every day. The PET membrane with 1 mm pores will become translucence in the presence of water, so we can observe the cells in the upper chamber or on bottom through a microscope. Spontaneously contracting cells appeared as clusters in outgrowths from the EBs. With daily gentle media changes and low EB density, the EBs continued to contract in culture for a period of observation of up to 36 days.Materials and Methods Generation of aMHC-GFP Transgenic MiceTo generate aMHC-GFP transgenic mice, eGFP-Rex-Neomycin cDNA was sucloned into the expression vector containing amyosin heavy chain promoter [29]. This Plasmid (aMHC-eGFPRex-Neo, No. 21229) was obtained from Addgene. Pronuclear microinjection and other procedures were performed by Cyagen Biosciences according to the standard protocols. Genotyping was performed by PCR on tail DNA with the following primer: eGFP forward: 59-ACGTAAACGGCCACAAGTTC-39; eGFP backward: 59- GATCTTGAAGTTCACCTTGATGC-39.Cell Culture of ESCsMouse CGR8 ESCs, previously established from strain 129P2/ Ola mouse embryos by Smith et al. [30], w.