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A
mt‐RFP, ER‐GFP, and plasmids expressing the indicated proteins. Mitochondria‐ER colocalization was analyzed using Mander’s coefficient (n = 15 cells analyzed in three independent experiments). Data are presented as mean ± SEM.
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B
GFP and ERMITO‐RLuc and indicated expression vectors. After 24 h, the transfected cells were sorted and plated for another 24 h, after which RLuc was analyzed (n = 3 independent experiments). Data are presented as mean ± SEM.
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C
GFP and the indicated plasmids. After 48 h, mitochondrial Ca2+ was determined (n = 30 cells from 3 independent experiments). Data are presented as mean ± SEM.
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D
LAR‐GECO1 and the indicated plasmids. After 48 h ER Ca2+ was released with caffeine (20 mM) as indicated (n = 25–27 cells from three independent experiments). Data are presented as mean ± SEM.
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E
GFP and the indicated plasmid. After 48 h, the effect of caffeine‐induced (20 mM) ER Ca2+ release on mitochondrial Ca2+ was measured (n = 25 cells from three independent experiments). Data are presented as mean ± SEM.
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F–J
GFP and the indicated plasmids. (F) After 48 h, mitochondrial membrane potential was determined by measuring TMRM fluorescence. The values were normalized to surrounding untransfected cells. (n = 90 cells analyzed in three independent experiments). (G–I) After 24 h, the transfected cells were sorted and plated for another 24 h. (G) Cells were treated with 2‐DG (10 mM) for 6 h, and ATP levels were measured (n = 3 independent experiments). (H) Oxygen consumption was measured and (I) RCR and (J) SRC were calculated (n = 3 independent experiments). Data are presented as mean ± SEM.