Regulates Brain Energy Metabolism

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Gene Expressio n. (fold change. ) ... B5E2 PDK4 BDNF CYCS Cox5b. 0.0. 0.5. 1.0 ... (D) GSK3β protein and gene expression 48 hours following GSK3β siRNA.
Cell Reports, Volume 23

Supplemental Information

GSK3b Regulates Brain Energy Metabolism Stephen A. Martin, Dylan C. Souder, Karl N. Miller, Josef P. Clark, Abdul Kader Sagar, Kevin W. Eliceiri, Luigi Puglielli, T. Mark Beasley, and Rozalyn M. Anderson

4.0 nmol/mg

pO 2

Control siGSK3β

3.0 2.0

pGSK-3β/GSK-3β

0

60

Minutes

50

40

30

10

20

0

*

1.0

0

Relative Protein

NADt

UT 24h LiCl

Con GSK3β S9A

Tomm20

1.5

Gene Expression (fold change)

Minutes

UT

1.5

LiCl

1.0

1.0

0.5

0.5

0.0

0.0

CI

CII

CIII

CIV

PGC-1α

CV

DAPI

2.0

UT

LiCl + LiCl VIII VIII

90 kD 70 kD

0.5

*

1.5

*

Con

1.0 0.5

siGSK3β

0.0

UT 2h 24h

UT LiCl VIII

LiCl

pGSK3β

DAPI

Merged

LiCl + VIII

P Gene Expression (fold change)

UT

0

K

24h

PGC-1α

24h LiCl

0

N

* *

Tubulin

50 25

M

1.0

O

UT LiCl VIII LiCl+VIII

*

UT 24h LiCl

Relative Protein

25

0.0

0.5

*

*

*

75

J Stain Intensity (fold change)

100

Con siGSK3β

Relative Protein

I

50

1.5

* 1.0

0.0

75

L

100

Ponceau

n β Co SK3 siG 24h VIII

*

60

HA

n β Co SK3 siG

0.5

50

_

GSK3b

1.0

G

S9A

40

LiCl

*

*

24h LiCl 1.5

pcDNA3.1

2.0

0.0

24h 24h VIII LiCl + VIII

30

24h 24h UT LiCl

1.0

0.0

F

3.0

0.0

0

Ponceau

20

24h LiCl + VIII

0.5

siGSK3β

10

24h VIII

GSK3β

Control

pO 2

24h LiCl

ND ND

+

Membrane Potential

24h UT

2

1.0

Gene Expression (fold change)

Day 0

4

LiCl

UT 1m M 2. 5m M 5m M 15 m M

0

H

Membrane Potential

Relative Cell Death %

100

6

_

Relative Cell %

+

*

1.5

+

200

8

1.5

* * *

2.0

_

*

D

*

+

10

300

E

C

_

B

* vs. 24h UT + vs. 24h UT and 24h VIII

+

A

Con

2.5

*

2.0

siGSK3β

1.5 1.0 0.5 0.0

Pan

α1

α4

B5E2 PDK4 BDNF CYCS Cox5b

PGC-1α

Figure S1. (related to Fig. 1). Data show the impact of lithium on cell proliferation (A) and (B) cell death. (C) JC-1 measurement of mitochondrial membrane potential following LiCl dose-response in H4 glioma. (D) GSK3β protein and gene expression 48 hours following GSK3β siRNA transfection. (E) JC-1 measurement of mitochondrial membrane potential following GSK3b inhibitor VIII (15μM) in H4 glioma with GSK3β interference. (F) GSK3β protein and gene expression 48 hours following GSK3β−S9A transfection. (G) Basal oxygen consumption over time in H4 glioma treated with DMSO, LiCl (15mM), inhibitor VIII (15μM), and both LiCl (15mM) and inhibitor VIII (15μM), and (H) in H4 glioma with GSK3β interference. (I) Total NAD (NADt) levels, and immunodetection of Tomm 20 (J), complexes I, II, III, IV, and V proteins of the ETS (K), and pGSK3β/GSK3β ratio (L) following the indicated LiCl treatment (15mM) in H4 glioma. (M) Detection of PGC-1α protein in H4 glioma following the indicated treatment. (N) Immunodetection of PGC-1μM in H4 glioma with GSK3β interference. (O) Immunodetection of tubulin and pGSK3β following 24h LiCl treatment in H4 glioma. (P) Gene expression of PGC-1μM and indicated transcripts in H4 glioma with GSK3β interference. (n= 3-6 biological replicates per assay; data shown as average +/- SEM; *p

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