Insulin signaling and mitochondrial phenotype in response to insulin
resistance and pioglitazone. Control myotubes were exposed to 25
mm glucose, and the insulin resistant myotubes were exposed to 40
mm glucose and 100 nm insulin for 48 h. A
represents insulin-responsive signaling as shown by the representative Western
blots (pTyr, phosphotyrosine; cont, control; IR,
insulin resistance). B, transcript levels, expressed as % control, of
genes encoding for mitochondrial regulatory proteins (PPARγ,
peroxisome proliferator-activated receptor γ; NRF1, nuclear
respiratory factor 1; Tfam, mitochondrial transcription factor A and
SIRT1. C, steady-state mitochondrial electron transfer chain protein
levels (COX I and III, cytochrome c oxidase subunits I and III;
Cyt c, cytochrome c; ND 6, NADH dehydrogenase, subunit 6;
VDAC, voltage-dependent anion channel) as well as levels of
voltage-activated anion channel, SIRT1, and actin as a housekeeping protein;
D, relative mitochondrial genomic copy number (% control). E
shows insulin-responsive signaling comparing insulin-resistant to pioglitazone
(Pio)-treated insulin-resistant myotubes. F, transcript
levels, expressed as % control, of genes encoding for mitochondrial regulatory
proteins. G, steady-state mitochondrial electron transfer chain
protein levels comparing insulin-resistant to insulin-resistant myotubes
exposed to pioglitazone. H, relative mitochondrial genomic copy
number (% control). The asterisk represents a p < 0.05
versus the respective control in this and all subsequent figures
(unless otherwise stated).