Rmed in a 2-dimensional format using DAPI as a nuclear stain. LDS-751 did not co-localise with the nuclear stain DAPI and, instead, LDS-751 overlapped exclusively with GFP imported to the mitochondria (Figure 3a). In addition, LDS-751 co-localised exclusively with mitosox red (Figure S5). Depolarisation of mitochondrial Z-360 custom synthesis membranes with valinomyocin inhibited the localisation of LDS-751 to mitochondria (Figure 3b). Mitochondrial localisation of LDS-751 has previously been reported in mouse fibroblasts and monocytes and, as for hESC, was dependent on polarised mitochondrial membranes [41]. Thus, LDS-751 can be used as a tool for tracking mitochondria in cultured cells.DiscussionIn order to investigate the role mitochondria play in regulating the balance between pluripotency and lineage commitment we developed a mitochondrial reporter hESC cell line that expresses a mitochondrially localized GFP, KMEL2. Importantly, we demonstrate that GFP expression is maintained in derivatives from all germ layers when KMEL2 hESC differentiate. The KMEL2 hESC line also facilitated the identification of mitochondrial biogenic reagents that promote differentiation of primitive mesendoderm.Tools for in vivo Mt AnalysisIn this study we developed two approaches to identifying and tracking mitochondrial localisation in hESC and their differentiated progeny. Firstly, we developed a mitochondrial reporter hESC cell line that produced a GFP construct tagged to a mitochondrial import sequence as has been shown for multiple cell types [45,46]. The reporter line, dubbed KMEL2, showed colocalisation of GFP with 
specific antibodies to mitochondria (Figure 2a), expressed pluripotency markers Oct-4 and SSEA-4 (Figure 2b) and retained a normal karyotype post transfection (Figure 2d). KMEL2 is particularly useful for tracking mitochondrial localisation and structural alterations during differentiation. Mitochondrial tracking may be important in therapeutic 
applications, for example the clumping of mitochondria in cellular prolongations during hESC neural differentiation is a characteristic phenotype of mitochondrial disorders such as ARSACS [7]. Secondly, we show that in hESC, LDS-751 co-localised specifically with GFP in the KMEL2 line and showed no significant overlap with the nuclear stain DAPI (Figure 3a). Whilst LDS-751 has been previously used as a nuclear marker [47] we show that mitochondrial localisation in hESCs is dependent on mitochondrial membrane polarisation as treatment with the depolarising agent valinomycin blocked mitochondrial specific staining (Figure 3b).Mitochondrial Localisation During Differentiation of All Three Germ LayersDuring hESC differentiation significant changes occur in mitochondrial metabolism, morphology and energy output (oxidative phosphorylation vs. glycolysis) [15,18,20]. However, little information is available on localisation and morphology of mitochondria during lineage specific differentiation. We used the KMEL2 reporter line and LDS-751 to track mitochondria during retinoic acid driven 52232-67-4 manufacturer neuroectoderm differentiation. Consistent with previous data [2,15], mitochondria in hESC prior to differentiation were closely localised to the periphery of the nucleus in dense clusters shown with both KMEL2 and LDS-751 (Figure 2b, 3b and 5a). In contrast, KMEL2 derived Nestin and MAP2C positive cells had mitochondria dispersed throughout the cell in granular and thread-like patterns (Figure 4a and Figure S4), as previously reported in adult ce.Rmed in a 2-dimensional format using DAPI as a nuclear stain. LDS-751 did not co-localise with the nuclear stain DAPI and, instead, LDS-751 overlapped exclusively with GFP imported to the mitochondria (Figure 3a). In addition, LDS-751 co-localised exclusively with mitosox red (Figure S5). Depolarisation of mitochondrial membranes with valinomyocin inhibited the localisation of LDS-751 to mitochondria (Figure 3b). Mitochondrial localisation of LDS-751 has previously been reported in mouse fibroblasts and monocytes and, as for hESC, was dependent on polarised mitochondrial membranes [41]. Thus, LDS-751 can be used as a tool for tracking mitochondria in cultured cells.DiscussionIn order to investigate the role mitochondria play in regulating the balance between pluripotency and lineage commitment we developed a mitochondrial reporter hESC cell line that expresses a mitochondrially localized GFP, KMEL2. Importantly, we demonstrate that GFP expression is maintained in derivatives from all germ layers when KMEL2 hESC differentiate. The KMEL2 hESC line also facilitated the identification of mitochondrial biogenic reagents that promote differentiation of primitive mesendoderm.Tools for in vivo Mt AnalysisIn this study we developed two approaches to identifying and tracking mitochondrial localisation in hESC and their differentiated progeny. Firstly, we developed a mitochondrial reporter hESC cell line that produced a GFP construct tagged to a mitochondrial import sequence as has been shown for multiple cell types [45,46]. The reporter line, dubbed KMEL2, showed colocalisation of GFP with specific antibodies to mitochondria (Figure 2a), expressed pluripotency markers Oct-4 and SSEA-4 (Figure 2b) and retained a normal karyotype post transfection (Figure 2d). KMEL2 is particularly useful for tracking mitochondrial localisation and structural alterations during differentiation. Mitochondrial tracking may be important in therapeutic applications, for example the clumping of mitochondria in cellular prolongations during hESC neural differentiation is a characteristic phenotype of mitochondrial disorders such as ARSACS [7]. Secondly, we show that in hESC, LDS-751 co-localised specifically with GFP in the KMEL2 line and showed no significant overlap with the nuclear stain DAPI (Figure 3a). Whilst LDS-751 has been previously used as a nuclear marker [47] we show that mitochondrial localisation in hESCs is dependent on mitochondrial membrane polarisation as treatment with the depolarising agent valinomycin blocked mitochondrial specific staining (Figure 3b).Mitochondrial Localisation During Differentiation of All Three Germ LayersDuring hESC differentiation significant changes occur in mitochondrial metabolism, morphology and energy output (oxidative phosphorylation vs. glycolysis) [15,18,20]. However, little information is available on localisation and morphology of mitochondria during lineage specific differentiation. We used the KMEL2 reporter line and LDS-751 to track mitochondria during retinoic acid driven neuroectoderm differentiation. Consistent with previous data [2,15], mitochondria in hESC prior to differentiation were closely localised to the periphery of the nucleus in dense clusters shown with both KMEL2 and LDS-751 (Figure 2b, 3b and 5a). In contrast, KMEL2 derived Nestin and MAP2C positive cells had mitochondria dispersed throughout the cell in granular and thread-like patterns (Figure 4a and Figure S4), as previously reported in adult ce.