Dysregulation of the mammalian target of rapamycin (mTOR) signaling, which is mediated by two structurally and functionally distinct complexes, mTORC1 and mTORC2, has been implicated in several neurological disorders1,2,3. Individuals carrying loss-of-function mutations in the phosphatase and tensin homolog (PTEN) gene, a negative regulator of mTOR signaling, are prone to developing macrocephaly, autism spectrum disorder (ASD), seizures and intellectual disability2,4,5. It is generally believed that the neurological symptoms associated with loss of PTEN and other mTORopathies (for example, mutations in the tuberous sclerosis genes TSC1 or TSC2) are due to hyperactivation of mTORC1-mediated protein synthesis1,2,4,6,7. Using molecular genetics, we unexpectedly found that genetic deletion of mTORC2 (but not mTORC1) activity prolonged lifespan, suppressed seizures, rescued ASD-like behaviors and long-term memory, and normalized metabolic changes in the brain of mice lacking Pten. In a more therapeutically oriented approach, we found that administration of an antisense oligonucleotide (ASO) targeting mTORC2’s defining component Rictor specifically inhibits mTORC2 activity and reverses the behavioral and neurophysiological abnormalities in adolescent Pten-deficient mice. Collectively, our findings indicate that mTORC2 is the major driver underlying the neuropathophysiology associated with Pten-deficiency, and its therapeutic reduction could represent a promising and broadly effective translational therapy for neurological disorders where mTOR signaling is dysregulated.
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The data supporting the findings of this study are available in this paper or the Supplementary Information. Full uncropped blots are available as Source data. Any other raw data that support the findings of this study are available from the corresponding author upon reasonable request. The request for Rictor-ASO will be promptly reviewed by Ionis Pharmaceuticals to verify that the request is subject to any intellectual property confidential obligations. If not, the ASO will be available upon completion of a standard Material Transfer Agreement with Ionis Pharmaceuticals.
Ehninger, D. & Silva, A. J. Rapamycin for treating tuberous sclerosis and autism spectrum disorders. Trends Mol. Med. 17, 78–87 (2011).
Winden, K. D., Ebrahimi-Fakhari, D. & Sahin, M. Abnormal mTOR activation in autism. Annu. Rev. Neurosci. 41, 1–23 (2018).
Costa-Mattioli, M. & Monteggia, L. M. mTOR complexes in neurodevelopmental and neuropsychiatric disorders. Nat. Neurosci. 16, 1537–1543 (2013).
Zhou, J. & Parada, L. F. PTEN signaling in autism spectrum disorders. Curr. Opin. Neurobiol. 22, 873–879 (2012).
Knafo, S. & Esteban, J. A. PTEN: local and global modulation of neuronal function in health and disease. Trends Neurosci. 40, 83–91 (2017).
Kelleher, R. J. 3rd & Bear, M. F. The autistic neuron: troubled translation? Cell 135, 401–406 (2008).
Hoeffer, C. A. & Klann, E. mTOR signaling: at the crossroads of plasticity, memory and disease. Trends Neurosci. 33, 67–75 (2010).
Lipton, J. O. & Sahin, M. The neurology of mTOR. Neuron 84, 275–291 (2014).
Wullschleger, S., Loewith, R. & Hall, M. N. TOR signaling in growth and metabolism. Cell 124, 471–484 (2006).
Saxton, R. A. & Sabatini, D. M. mTOR signaling in growth, metabolism and disease. Cell 169, 361–371 (2017).
Sarbassov, D. D. et al. Rictor, a novel binding partner of mTOR, defines a rapamycin-insensitive and raptor-independent pathway that regulates the cytoskeleton. Curr. Biol. 14, 1296–1302 (2004).
Hay, N. & Sonenberg, N. Upstream and downstream of mTOR.Genes Dev. 18, 1926–1945 (2004).
Buffington, S. A., Huang, W. & Costa-Mattioli, M. Translational control in synaptic plasticity and cognitive dysfunction. Annu. Rev. Neurosci. 37, 17–38 (2014).
Crino, P. B. The mTOR signalling cascade: paving new roads to cure neurological diseaseNat. Rev. Neurol. 12, 379–392 (2016).
Zhou, J. et al. Pharmacological inhibition of mTORC1 suppresses anatomical, cellular and behavioral abnormalities in neural-specific Pten knock-out mice. J. Neurosci. 29, 1773–1783 (2009).
Ljungberg, M. C., Sunnen, C. N., Lugo, J. N., Anderson, A. E. & D’Arcangelo, G. Rapamycin suppresses seizures and neuronal hypertrophy in a mouse model of cortical dysplasia. Dis. Models Mech. 2, 389–398 (2009).
Nguyen, L. H. et al. mTOR inhibition suppresses established epilepsy in a mouse model of cortical dysplasia. Epilepsia 56, 636–646 (2015).
Hobert, J. A., Embacher, R., Mester, J. L., Frazier, T. W.II & Eng, C. Biochemical screening and PTEN mutation analysis in individuals with autism spectrum disorders and macrocephaly. Eur. J. Hum. Genet 22, 273–276 (2014).
Tilot, A. K. et al. Neural transcriptome of constitutional Pten dysfunction in mice and its relevance to human idiopathic autism spectrum disorder. Mol. Psychiatry 21, 118–125 (2016).
McBride, K. L. et al. Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephaly.Autism Res. 3, 137–141 (2010).
Hu, W. F., Chahrour, M. H. & Walsh, C. A. The diverse genetic landscape of neurodevelopmental disorders. Annu. Rev. Genomics Hum. Genet. 15, 195–213 (2014).
Mirzaa, G. M. & Poduri, A. Megalencephaly and hemimegalencephaly: breakthroughs in molecular etiology. Am. J. Med. Genet. C Semin. Med. Genet. 166C, 156–172 (2014).
Kwon, C. H. et al. Pten regulates neuronal arborization and social interaction in mice. Neuron 50, 377–388 (2006).
Backman, S. A. et al. Deletion of Pten in mouse brain causes seizures, ataxia and defects in soma size resembling Lhermitte–Duclos disease. Nat. Genet. 29, 396–403 (2001).
Kwon, C. H. et al. Pten regulates neuronal soma size: a mouse model of Lhermitte–Duclos disease. Nat. Genet. 29, 404–411 (2001).
Ostendorf, A. P. & Wong, M. mTOR inhibition in epilepsy: rationale and clinical perspectives. CNS Drugs 29, 91–99 (2015).
Noebels, J. L Single-gene determinants of epilepsy comorbidity. Cold Spring Harb. Perspect. Med. 5, a022756 (2015).
Fombonne, E. The epidemiology of autism: a review. Psychol. Med. 29, 769–786 (1999).
Kazdoba, T. M. et al. Translational mouse models of autism: advancing toward pharmacological therapeutics. Curr. Top. Behav. Neurosci. 28, 1–52 (2016).
Jiang, Y. H. & Ehlers, M. D. Modeling autism by SHANK gene mutations in mice. Neuron 78, 8–27 (2013).
American Psychiatric Association & American Psychiatric Association DSM-5 Task Force Diagnostic and Statistical Manual of Mental Disorders: DSM-5 (American Psychiatric Association, 2013).
Lopez, B. R., Lincoln, A. J., Ozonoff, S. & Lai, Z. Examining the relationship between executive functions and restricted, repetitive symptoms of autistic disorder. J. Autism Dev. Disord. 35, 445–460 (2005).
Stoica, L. et al. Selective pharmacogenetic inhibition of mammalian target of rapamycin complex I (mTORC1) blocks long-term synaptic plasticity and memory storage. Proc. Natl Acad. Sci. USA 108, 3791–3796 (2011).
Huang, W. et al. mTORC2 controls actin polymerization required for consolidation of long-term memory. Nat. Neurosci. 16, 441–448 (2013).
Garcia-Cao, I. et al. Systemic elevation of PTEN induces a tumor-suppressive metabolic state. Cell 149, 49–62 (2012).
Hagiwara, A. et al. Hepatic mTORC2 activates glycolysis and lipogenesis through Akt, glucokinase and SREBP1c. Cell Metab. 15, 725–738 (2012).
Masui, K. et al. mTOR complex 2 controls glycolytic metabolism in glioblastoma through FoxO acetylation and upregulation of c-Myc. Cell Metab. 18, 726–739 (2013).
Panasyuk, G. et al. PPARγ contributes to PKM2 and HK2 expression in fatty liver. Nat. Commun. 3, 672 (2012).
Robey, R. B. & Hay, N. Is Akt the ‘Warburg kinase’? Akt-energy metabolism interactions and oncogenesis. Semin. Cancer Biol. 19, 25–31 (2009).
Rinaldi, C. & Wood, M. J. A. Antisense oligonucleotides: the next frontier for treatment of neurological disorders. Nat. Rev. Neurol. 14, 9–21 (2018).
Vickers, T. A. et al. Efficient reduction of target RNAs by small interfering RNA and RNase H-dependent antisense agents. A comparative analysis. J. Biol. Chem. 278, 7108–7118 (2003).
Cioffi, C. L. et al. Selective inhibition of A-Raf and C-Raf mRNA expression by antisense oligodeoxynucleotides in rat vascular smooth muscle cells: role of A-Raf and C-Raf in serum-induced proliferation. Mol. Pharmacol. 51, 383–389 (1997).
Zhang, H. et al. Reduction of liver Fas expression by an antisense oligonucleotide protects mice from fulminant hepatitis. Nat. Biotechnol. 18, 862–867 (2000).
Langmead, B., Trapnell, C., Pop, M. & Salzberg, S. L. Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biol. 10, R25 (2009).
Zhu, P. J. et al. Suppression of PKR promotes network excitability and enhanced cognition by interferon-γ-mediated disinhibition. Cell 147, 1384–1396 (2011).
Buffington, S. A. et al. Microbial reconstitution reverses maternal diet-induced social and synaptic deficits in offspring. Cell 165, 1762–1775 (2016).
Silverman, J. L., Yang, M., Lord, C. & Crawley, J. N. Behavioural phenotyping assays for mouse models of autism. Nat. Rev. Neurosci. 11, 490–502 (2010).
Deacon, R. M. & Rawlins, J. N. T-maze alternation in the rodent. Nat. Protoc. 1, 7–12 (2006).
Johnson, J. L., Huang, W., Roman, G. & Costa-Mattioli, M. TORC2: a novel target for treating age-associated memory impairment. Sci. Rep. 5, 15193 (2015).
Zhu, P. J., Chen, C. J., Mays, J., Stoica, L. & Costa-Mattioli, M. mTORC2, but not mTORC1, is required for hippocampal mGluR-LTD and associated behaviors. Nat. Neurosci. 21, 799–802 (2018).
Huang, W et al. Translational control by eIF2α phosphorylation regulates vulnerability to the synaptic and behavioral effects of cocaine. eLife 5, e12052 (2016).
Ma, Y., Bai, R. K., Trieu, R. & Wong, L. J. Mitochondrial dysfunction in human breast cancer cells and their transmitochondrial cybrids. Biochim. Biophys. Acta 1797, 29–37 (2010).
Frazier, A. E. & Thorburn, D. R. Biochemical analyses of the electron transport chain complexes by spectrophotometry. Methods Mol. Biol. 837, 49–62 (2012).
Venegas, V. & Halberg, M. C. Measurement of mitochondrial DNA copy number. Methods Mol. Biol. 837, 327–335 (2012).
Swayze, E. E. et al. Antisense oligonucleotides containing locked nucleic acid improve potency but cause significant hepatotoxicity in animals. Nucleic Acids Res. 35, 687–700 (2007).
We thank A. Placzek and members of the Costa-Mattioli laboratory for comments on the manuscript. This work was supported by funds to M.C.-M. (NIMH 096816, Department of Defense AR120254 and Sammons Enterprises), J.N. (NINDS NS29709) and J.C. (NS085171).
P.J.-N. and F.R. are employed by Ionis Pharmaceutical, a company that develops ASO therapies. The authors declare no other competing interests.
Peer review information Brett Benedetti was the primary editor on this article and managed its editorial process and peer review in collaboration with the rest of the editorial team.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
(a) Schematics of generation of forebrain neuron specific Pten-deficient (Pten fb-KO) and double knockout mice (Pten-Rptor fb-DKO and Pten-Rictor fb-DKO). (b-e) Representative western blot (b) and quantification show reduced PTEN levels in Pten fb-KO mice (c, n = 5, t = 5.22, P < 0.0001), Pten-Rptor fb-DKO (c, n = 5, t = 5.34, P < 0.0001) and Pten-Rictor fb-DKO (c, n = 5, t = 4.50, P = 0.0004) and reduced Raptor (d, n = 5 per group, vs. control t = 3.52, P = 0.0028) or Rictor (e, n = 5, t = 3.83, P = 0.0015) levels in the hippocampus of Pten-Rptor fb-DKO mice or Pten-Rictor fb-DKO mice, respectively. Representative western blot (f) and quantification (g-h) show increased mTORC1 (g, p-S6 at S240/244) and mTORC2 activity (h, p-Akt at S473) in cortex of Pten fb-KO mice (n = 6 per group, p-S6: t = 2.32, P = 0.03, p-Akt: t = 2.81, P = 0.0111). The increased mTORC1 activity in the cortex of Pten fb-KO mice was reduced in Pten-Rptor fb-DKO mice (n = 6, vs. Pten fb-KO, t = 2.87, P = 0.0091), but not in Pten-Rictor fb-DKO mice (n = 6, vs. Pten fb-KO, t = 0.13, P = 0.8958). By contrast, the increased mTORC2 activity in the cortex of Pten fb-KO mice was reduced in Pten-Rictor fb-DKO mice (t = 3.02, P = 0.0066), but not in Pten-Rptor fb-DKO mice (t = 3.92, P = 0.0009). Data are mean ± SEM. Statistics were based on one-way ANOVA followed by uncorrected two-sided Fisher’s LSD method for pairwise comparisons. n.s., not significant. Source data
Extended Data Fig. 2 Genetic inhibition of mTORC1 (but not mTORC2) reverses the increased brain/body weight ratio in Pten fb-KO mice.
(a) Crystal violet staining of mid-sagittal brain sections from control, Pten fb-KO mice, Pten-Rptor fb-DKO and Pten-Rictor fb-DKO mice (3 mice per group were used for the experiment). (b) Body weight of control (n = 11), Pten fb-KO (n = 9), Pten-Rictor fb-DKO mice (n = 13) and Pten-Rptor fb-DKO (n = 9) was similar (F3,38 = 0.93; P = 0.443). (c) Brain weight relative to body weight in control (n = 11, 0.94 ± 0.04%), Pten fb-KO (n = 9, 2.45 ± 0.34%, vs. control, t = 5.13, P < 0.0001), Pten-Rptor fb-DKO (n = 8, 2.12 ± 0.08%, vs. Pten fb-KO, t = 3.145, P = 0.0034) and Pten-Rictor fb-DKO mice (n = 11, 2.52 ± 0.07%, vs. Pten fb-KO, t = 0.21, P = 0.7810). Box graphs are presented as median, 25th percentile, 75th percentile, minimum, and maximum of the group. Statistics were based on one-way ANOVA followed by uncorrected two-sided Fisher’s LSD method for pairwise comparisons or paired t-test. n.s., not significant.
Extended Data Fig. 3 Genetic inhibition of mTORC2 (but not mTORC1) reverses the increased excitatory synaptic transmission in Pten fb-KO mice.
(a-c) Summary data (a-b) and sample traces (c) show increased frequency (a, Control n = 7, Pten fb-KO n = 6, t = 4.62, P < 0.0001), but not amplitude (b, Control n = 7, Pten fb-KO n = 6, t = 0.47, P = 0.641) of spontaneous excitatory postsynaptic currents (sEPSCs) in CA1 neurons from Pten fb-KO mice compared to control littermates. Unlike in Pten-Rptor fb-DKO mice (n = 9; a, c, Control vs. Pten-Rptor fb-DKO: t = 6.26, P < 0.0001), in Pten-Rictor fb-DKO mice (n = 5), sEPSC frequency is restored to control values (a, c, Control vs. Pten-Rictor fb-DKO: t = 0.86, P = 0.99). Data are mean ± SEM. Statistics are based on one-way ANOVA followed by uncorrected two-sided Fisher’s LSD method for pairwise comparisons. (d-f) Summary data (d-e) and sample traces (f) show similar frequency (d, Control n = 8, Pten fb-KO n = 14, t = 0.47, P = 0.636) and amplitude (e, Control n = 8, Pten fb-KO n = 14, t = 0.09, P = 0.925) of spontaneous inhibitory postsynaptic currents (sIPSCs) in CA1 neurons from control and Pten fb-KO mice. Statistics were based two-sided Student’s t-test Data are mean ± SEM. (g) Input-output curves in CA1 pyramidal neurons show that Pten fb-KO mice and Pten-Rptor fb-DKO mice fired more action potentials (APs) than control littermates at 350pA or higher current injection (n = 7 per group, control vs. Pten fb-KO, 350pA: t = 2.76, P = 0.020; 400 pA: t = 3.23, P = 0.0041; 450 pA: t = 4.13, P = 0.0002). By contrast, the increased excitability in Pten fb-KO mice is reduced in Pten-Rictor fb-DKO mice (n = 7 per group, Pten fb-KO vs. Pten-Rictor fb-DKO, 350 pA: t = 2.76, P = 0.020; 400 pA: t = 3.05, P = 0.010; 450 pA: t = 3.42, P = 0.002. Data are mean ± SEM. Statistics were based on two-way ANOVA followed by Bonferroni’s two-sided multiple comparison test. (h) Representative response elicited in CA1 pyramidal neurons (at -70 mV) upon injection of 400 pA for 500 ms.
Extended Data Fig. 4 Genetic inhibition of mTORC2 rescues the deficits in reciprocal social interaction and long-term object recognition memory in Pten fb-KO mice.
(a) Schematic of the reciprocal social interaction task. (b) Compared to controls (n = 11), Pten fb-KO mice (n = 9) show decreased social interaction (t = 3.42, P = 0.0023). The deficits in reciprocal social interaction are restored in Pten-Rictor fb-DKO mice (n = 7, vs. Pten fb-KO mice, t = 4.69, P < 0.0001). (c) Normal freezing responses in Pten fb-KO mice during training. All groups show similar freezing responses either before (naïve: control, n = 15 vs. Pten fb-KO, n = 12, t = 0.13, P = 0.8948; control vs. Pten-Rptor fb-DKO, n = 12, t = 0.32, P = 0.7941; control vs. Pten-Rictor fb-DKO, n = 12, t = 0.04, P = 0.9668) or immediately after training (post-shock: control vs. Pten fb-KO, t = 0.66, P = 0.5904; control vs. Pten-Rptor fb-DKO, t = 1.46, P = 0.1492; control vs. Pten-Rictor fb-DKO, t = 1.23, P = 0.2238). (d) Schematic of the object recognition task. (e) Pten fb-KO mice showed impaired long-term object recognition memory [control (n = 9), Pten fb-KO (n = 6), t = 4.89, P < 0.0001), which was rescued in Pten-Rictor fb DKO mice [Pten-Rictor fb DKO mice (n = 8) vs. Pten fb-KO mice, t = 3.71, P = 0.0014; Pten-Rictor fb DKO mice vs. control, t = 1.18, P = 0.2518]. Data are mean ± SEM. Statistics were based on two-way ANOVA followed by uncorrected two-sided Fisher’s LSD method for pairwise comparisons. n.s., not significant.
Extended Data Fig. 5 Selective increase in p-Akt in Pten fb-KO mice is reduced by genetic inhibition of mTORC2.
Representative western blots (a) and quantifications (b-d) show that compared to control mice, p-Akt at Ser473 (but not p-PKC or p-NDRG1) is the only mTORC2 downstream target whose activity is upregulated in the brain of Pten fb-KO mice [control vs. Pten fb-KO (n = 5-6 per group), p-Akt (b): t = 6.11, P < 0.0001, p-PKC (c): t = 0.64, P = 0.5291, p-NDRG1 (d): t = 0.69, P = 0.4983). As expected, genetic deletion of mTORC2 reduced the activity of all three mTORC2 targets (p-Akt, p-PKC and p-NDRG1) in the brain of Pten-Rictor fb-DKO (n = 6, vs. control p-Akt (b): t = 0.89, P = 0.3903, p-PKC (c): t = 4.56, P = 0.0004, p-NDRG1 (d): t = 2.31, P = 0.0359; vs. Pten fb-KO, p-Akt: t = 7.33, P < 0.0001, p-PKC: t = 3.91, P = 0.0014, p-NDRG1: t = 2.99, P = 0.0090). Compared to Pten fb-KO mice, genetic deletion of mTORC1 in Pten-Rptor fb-DKO did not decrease p-Akt (e-f:,Pten fb-KO (n = 4) vs. Pten-Rptor fb-DKO (n = 6), t = 4.59, P = 0.0005; control (n = 5) vs. Pten-Rptor fb-DKO, t = 9.31, P < 0.0001), p-PKC (e,g: Pten fb-KO (n = 4) vs. Pten-Rptor fb-DKO (n = 5), t = 0.65, P = 0.5332; control (n = 4) vs. Pten-Rptor fb-DKO, t = 0.73, P = 0.4820) or p-NDRG1 (e,h: Pten fb-KO (n = 4) vs. Pten-Rptor fb-DKO (n = 5), t = 1.19, P = 0.2581; control (n = 4) vs. Pten-Rptor fb-DKO, t = 0.46, P = 0.6527). Data are mean ± SEM. Statistics were based on one-way ANOVA followed by uncorrected two-sided Fisher’s LSD method for pairwise comparisons. n.s., not significant. Source data
Extended Data Fig. 6 Genetic inhibition of mTORC2 rescues the changes in glucose metabolism in the brain of Pten fb-KO mice.
(a) Schematic of mTORC2 regulation of glucose metabolism through the phosphorylation of Akt. (b-d) Metabolomic study revealed an increase in glycolysis metabolites in Pten fb-KO mice, which is normalized when mTORC2, but not mTORC1, is inhibited. The level of glucose (b), glucose-6-phosphate (c) and lactate (d) were increased in the cortex of Pten fb-KO mice (control (n = 8) vs. Pten fb-KO (n = 7): glucose, t = 3.51, P = 0.0017; glucose-6-phosphate, t = 2.77, P = 0.0103; lactate, t = 2.41, P = 0.024). The changes in glucose metabolism are reversed in Pten-Rictor fb-DKO mice (n = 7, vs. control: glucose, t = 0.067, P = 0.9469; glucose-6-phosphate, t = 0.39, P = 0.7009; lactate t = 1.39, P = 0.1771), but not in Pten-Rptor fb-DKO mice [Pten-Rictor fb-KO mice (n = 7) vs. Pten-Rptor fb-DKO (n = 7): glucose, t = 1.07, P = 0.2962; glucose-6-phosphate, t = 1.55, P = 0.1355; lactate t = 0.39, P = 0.6993]. Data are mean ± SEM. Statistics were based on one-way ANOVA followed by uncorrected two-sided Fisher’s LSD method for pairwise comparisons. n.s., not significant.
Extended Data Fig. 7 No major changes in mitochondria number, electron transport chain function or the abundance of TCA cycle metabolites in the brain of Pten fb-KO mice.
(a-b) No differences in mitochondria DNA copy number (a, n = 5 per group, F3,16 = 0.21, P = 0.1229) or ETC enzyme activity [b, control (n = 4) Pten fb-KO (n = 3), Pten-Rptor fb-KO (n = 3), Pten-Rictor fb-KO (n = 3), F3,9 = 0.16, P = 0.3782) were observed between the cortexes of control and Pten-deficient mice. (c) The abundance of TCA cycle metabolites did not dramatically change in the brain of Pten fb-KO mice [control (n = 8) vs. Pten fb-KO (n = 7): citrate, t = 0.60, P = 0.5512; alpha-ketoglutarate, t = 1.45, P = 0.1545; malate, t = 1.79, P = 0.0858, fumarate, t = 0.3983, P = 0.69. Control vs. Pten-Rptor fb-DKO (n = 7): citrate, t = 0.95, P = 0.3522; alpha-ketoglutarate, t = 0.62, P = 0.5404; malate, t = 0.41, P = 0.6833; fumarate, t = 1.37, P = 0.1816. control vs. Pten-Rictor fb-DKO n = 7, citrate, t = 0.5512, P = 0.5864; alpha-ketoglutarate, t = 0.2, P = 0.8455; malate, t = 0.43, P = 0.6687, fumarate, t = 0.39, P = 0.6973]. Data are mean ± SEM. Statistics were based on one-way ANOVA followed by uncorrected two-sided Fisher’s LSD method for pairwise comparisons. n.s., not significant.
Extended Data Fig. 8 ASO-A (Rictor-ASO) reduces mTORC2 (but not mTORC1) activity in cortical neurons in culture.
(a-b) Cortical neurons were treated for 72 hours with different ASOs (10 μM) designed to target Rictor mRNA. Representative western blots (a) and quantification (b) show that ASO-A strongly reduces both Rictor protein level (n = 4 per group, t6 = 10.94, P = 0.0001) and mTORC2 activity (t6 = 7.25, P = 0.0010), but had no effect on mTORC1 activity (t6 = 0.33, P = 0.9846). Data are mean ± SEM. Values were compared relative to the vehicle treated group and statistics were based on two-sided t-test comparisons. n.s., not significant. Source data
Control mice were injected with Rictor-ASO and monitored for 5 weeks after injection. (a) Rictor-ASO reduced Rictor mRNA levels in spinal cord (n = 4 per group, t6 = 40.76, P < 0.0001), cortex (n = 4 per group, t6 = 16.77, P < 0.0001) and cerebellum (n = 4 per group, t6 = 11.44, P < 0.001). (b) Rictor-ASO-injected mice showed normal weight gain several weeks post-injection (F5,30 = 2,10, P = 0.0875). (c) mRNA expression of gliosis marker (Gfap) and microglia inflammatory markers (Aif1, CD68) were normal in the brain of Rictor-ASO injected mice (Aif1: n = 4 per group, t6 = 0.60, P = 0.544; CD68: n = 4 per group, t6 = 2.12, P = 0.783; Gfap: n = 4 per group, t6 = 0.17, P = 0.8673). Circles represent number of animals per condition. (d) Control mice were injected with Rictor-ASO and the hippocampus was isolated 2 weeks post-injection. Rictor-ASO selectively reduces Rictor mRNA levels, but did not change the expression of Nisch, Plus7, GM6943, GM9265, GM9295 and GM5954 (n = 4 per group, PBS vs. Rictor-ASO: Rictor: t6 = 3.06, P = 0.0223; Nisch: t6 = 1.11, P = 0.3094; Pus7l: t6 = 1.40, P = 0.2106; GM6943: t6 = 0.54, P = 0.6061, GM9265: t6 = 0.48, P = 0.6513; GM9295: t6 = 0.39, P = 0.71; GM5954: t6 = 1.19, P = 0.2763). Data are mean ± SEM. n represents one biological independent mouse. Statistics were based on two-sided t-test comparisons. n.s., not significant.
Extended Data Fig. 10 A control ASO (Control-ASO) failed to reduce Rictor mRNA levels and inhibit mTORC2 activity.
(a) Treatment with Control-ASO did not reduce Rictor mRNA [PBS (n = 6) vs. Control-ASO (n = 4), t8 = 1.88, P = 0.0968]. Representative western blot image (b) and quantification of (c-d) show that Control-ASO did not decrease Rictor protein levels (n = 4 per group, PBS vs. control-ASO t6 = 0.57, P = 0.5864) or mTORC2 activity (n = 4 per group, PBS vs. control-ASO, t6 = 0.71, P = 0.5018). Data are mean ± SEM. Statistics were based on two-sided t-test comparisons. n.s., not significant. Source Data
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Chen, C., Sgritta, M., Mays, J. et al. Therapeutic inhibition of mTORC2 rescues the behavioral and neurophysiological abnormalities associated with Pten-deficiency. Nat Med 25, 1684–1690 (2019). https://doi.org/10.1038/s41591-019-0608-y
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