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. Author manuscript; available in PMC: 2022 May 5.
Published in final edited form as: Neuron. 2021 Mar 24;109(9):1479–1496.e6. doi: 10.1016/j.neuron.2021.03.008

Figure 2. Protein levels and activity of downstream mTOR effectors in bipolar disorder and schizophrenia DLPFC.

Figure 2.

A and B. Blots show phospho and total levels of ULK1, p70S6K, and 4E-BP1 in DLPFC homogenates. Diagnosis (S=schizophrenia, C=control, B=bipolar disorder), sex (M=male, F=female), and absence (−) or presence (+) of psychosis indicated. Figure S2 for the remaining blots.

C. p-ULK1 (S757) in DLPFC homogenates. *p<0.05 with multiple comparison correction; t=p<0.05 with direct comparison. Table S2 for statistical details.

D. p-ULK1 (S777) in DLPFC homogenates. t=p<0.05 with direct comparison. Table S2 for statistical details.

E. Total ULK1 in DLPFC homogenates. No differences between groups detected. Table S2 for statistical details.

F. Phospho-p70S6K (T421/S424) in DLPFC homogenates. No differences between groups detected. Table S2 for statistical details.

G. Phospho-p70S6K (T389) in DLPFC homogenates. No differences between groups detected. Table S2 for statistical details.

H. Total p70S6K in DLPFC homogenates. *p<0.05 with multiple comparison correction. Table S2 for statistical details.

I. p-4E-BP1 (T37/46) in DLPFC homogenate. No differences between groups detected. Table S2 for statistical details.

J. Total 4E-BP1 in DLPFC homogenates. No differences between groups detected. Table S2 for statistical details.

Summary data are the mean+SEM. n=35 control (26 male, 9 female), 12 BP-no psychosis (7 male, 5 female), 20 BP-psychosis (8 male, 12 female), 35 schizophrenia (26 male, 9 female)

See also Table S2 and Figure S2