Solinas et al. 10.1073/pnas.0607626103.

Supporting Figures

Files in this Data Supplement:

Supporting Figure 6
Supporting Figure 7
Supporting Figure 8
Supporting Figure 9
Supporting Figure 10
Supporting Figure 11




Supporting Figure 6

Fig. 6. Alloxan and steptozotocin induced insulin-dependent diabetes in mice. Fasted mice received a single injection of either alloxan or STZ. Blood glucose levels were measured at 3 and 10 days after injection or at an equivalent time in mock-injected mice.





Supporting Figure 7

Fig. 7. Quantification of the JNK kinase assays shown in Fig. 1B.





Supporting Figure 8

Fig. 8. Quantification of the PI3K assays shown in Fig. 2B





Supporting Figure 9

Fig. 9. JNK1 is required for PA-induced insulin resistance in primary hepatocytes. (A) Primary hepatocytes from from Jnk1-/- mice were left uninfected, or were infected with either a GFP-expressing lentivirus, or a JNK1-expressing lentivirus. After 3 days, the cells were treated for 2 h with PA before addition of insulin as indicated. After 10 min, IRS1 Ser-307 and Akt Ser-473 phosphorylation were examined by immunoblotting. (B) Primary hepatocytes were treated as above, and PI3K activity was measured in immunocomplexes isolated with phosphotyrosine-specific antibodies.





Supporting Figure 10

Fig. 10. PA induces sustained JNK activation in primary pancreatic islets. Primary islets were incubated for 12 h with palmitate (0.5 mM) in the presence of either 5.5 or 16.7 mM glucose, and JNK activity was measured.





Supporting Figure 11

Fig. 11. PA induces IRS1 Ser-307 phosphorylation in b-cells. Primary pancreatic islets were incubated for 12 h with PA (0.5 mM) with or without D-JNKi. IRS1 Ser-307 phosphorylation was analyzed by immunoblotting.