Tuberous Sclerosis Complex Activity Is Required to Control Neuronal Stress Responses in an mTOR-Dependent Manner
Open accessAbstract
Tuberous sclerosis complex (TSC) is a neurogenetic disorder caused by loss-of-function mutations in either the TSC1 or TSC2 genes and frequently results in prominent CNS manifestations, including epilepsy, mental retardation, and autism spectrum disorder. The TSC1/TSC2 protein complex plays a major role in controlling the Ser/Thr kinase mammalian target of rapamycin (mTOR), which is a master regulator of protein synthesis and cell growth. In this study, we show that endoplasmic reticulum (ER) stress regulates TSC1/TSC2 complex to limit mTOR activity. In addition, Tsc2-deficient rat hippocampal neurons and brain lysates from a Tsc1-deficient mouse model demonstrate both elevated ER and oxidative stress. In Tsc2-deficient neurons, the expression of stress markers such as CHOP and HO-1 is increased, and this increase is completely reversed by the mTOR inhibitor rapamycin both in vitro and in vivo. Neurons lacking a functional TSC1/TSC2 complex have increased vulnerability to ER stress-induced cell death via the activation of the mitochondrial death pathway. Importantly, knockdown of CHOP reduces oxidative stress and apoptosis in Tsc2-deficient neurons. These observations indicate that ER stress modulates mTOR activity through the TSC protein complex and that ER stress is elevated in cells lacking this complex. They also suggest that some of the neuronal dysfunction and neurocognitive deficits seen in TSC patients may be attributable to ER and oxidative stress and therefore potentially responsive to agents moderating these pathways.
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Neurons without a functional TSC1/TSC2 complex have increased vulnerability to endoplasmic reticulum stress-induced cell death through activation of the mitochondrial death pathway.
“neurons without a functional TSC1/TSC2 complex have been shown to have increased vulnerability to endoplasmic reticulum stress-induced cell death through the activation of the mitochondrial death pathway [55].”
From Tuberous Sclerosis Protein 2 (TSC2) Modulates CCN4 Cytoprotection During Apoptotic Amyloid Toxicity in Microglia (2013) · cites this paper as [55]
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Cites
Signal integration in the endoplasmic reticulum unfolded protein response
Ron, D., & Walter, P. (2007) · Nature reviews. Molecular cell biology · doi:10.1038/nrm2199 · Cited by 6,499 · see citing works
An Integrated Stress Response Regulates Amino Acid Metabolism and Resistance to Oxidative Stress
Harding, H. P., Zhang, Y., Zeng, H., Novoa, I., Lu, P. D., Calfon, M. A., Sadri, N., Yun, C., Popko, B., Paules, R. S., et al. (2003) · Molecular Cell · doi:10.1016/s1097-2765(03)00105-9 · Cited by 3,336 · see citing works
Regulated Translation Initiation Controls Stress-Induced Gene Expression in Mammalian Cells
Harding, H. P., Novoa, I., Zhang, Y., Zeng, H., Wek, R. C., Schapira, M., & Ron, D. (2000) · Molecular Cell · doi:10.1016/s1097-2765(00)00108-8 · Cited by 3,281 · see citing works
TSC2 is phosphorylated and inhibited by Akt and suppresses mTOR signalling
Inoki, K., Li, Y., Zhu, T., Wu, J., & Guan, K.-L. (2002) · Nature Cell Biology · doi:10.1038/ncb839 · Cited by 3,083 · see citing works
Urano, F., Wang, X.-Z., Bertolotti, A., Zhang, Y.-H., Chung, P., Harding, H., & Ron, D. (2000) · Science · doi:10.1126/science.287.5453.664 · Cited by 3,081 · see citing works
Dynamic interaction of BiP and ER stress transducers in the unfolded-protein response
Bertolotti, A., Zhang, Y., Hendershot, L. M., Harding, H. P., & Ron, D. (2000) · Nature Cell Biology · doi:10.1038/35014014 · Cited by 2,871 · see citing works
Roles of CHOP/GADD153 in endoplasmic reticulum stress
Oyadomari, S., & Mori, M. (2003) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401373 · Cited by 2,833 · see citing works
Marciniak, S. J., Yun, C. Y., Oyadomari, S., Novoa, I., Zhang, Y., Jungreis, R., Nagata, K., Harding, H. P., & Ron, D. (2004) · Genes & Development · doi:10.1101/gad.1250704 · Cited by 2,004 · see citing works
McCullough, K. D., Martindale, J. L., Klotz, L., Aw, T. Y., & Holbrook, N. J. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.4.1249-1259.2001 · Cited by 1,895 · see citing works
The Tuberous Sclerosis Complex
Crino, P. B., Nathanson, K. L., & Henske, E. P. (2006) · New England Journal of Medicine · doi:10.1056/nejmra055323 · Cited by 1,793 · see citing works
Promoting Axon Regeneration in the Adult CNS by Modulation of the PTEN/mTOR Pathway
Park, K. K., Liu, K., Hu, Y., Smith, P. D., Wang, C., Cai, B., Xu, B., Connolly, L., Kramvis, I., Sahin, M., et al. (2008) · Science · doi:10.1126/science.1161566 · Cited by 1,686 · see citing works
Self-citationManning, B. D., Tee, A. R., Logsdon, M. N., Blenis, J., & Cantley, L. C. (2002) · Molecular Cell · doi:10.1016/s1097-2765(02)00568-3 · Cited by 1,555 · see citing works
Organelle-specific initiation of cell death pathways
Ferri, K. F., & Kroemer, G. (2001) · Nature Cell Biology · doi:10.1038/ncb1101-e255 · Cited by 1,455 · see citing works
A trip to the ER: coping with stress
Rutkowski, D. T., & Kaufman, R. J. (2003) · Trends in Cell Biology · doi:10.1016/j.tcb.2003.11.001 · Cited by 1,364 · see citing works
Coupling endoplasmic reticulum stress to the cell death program
Rao, R. V., Ellerby, H. M., & Bredesen, D. E. (2004) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401378 · Cited by 1,208 · see citing works
Lee, K., Tirasophon, W., Shen, X., Michalak, M., Prywes, R., Okada, T., Yoshida, H., Mori, K., & Kaufman, R. J. (2002) · Genes & Development · doi:10.1101/gad.964702 · Cited by 1,055 · see citing works
Orchestrating the unfolded protein response in health and disease
Kaufman, R. J. (2002) · Journal of Clinical Investigation · doi:10.1172/jci0216886 · Cited by 1,015 · see citing works
Akt regulates growth by directly phosphorylating Tsc2
Potter, C. J., Pedraza, L. G., & Xu, T. (2002) · Nature Cell Biology · doi:10.1038/ncb840 · Cited by 959 · see citing works
Tripartite Management of Unfolded Proteins in the Endoplasmic Reticulum
Mori, K. (2000) · Cell · doi:10.1016/s0092-8674(00)80855-7 · Cited by 918 · see citing works
Reversal of learning deficits in a Tsc2+/− mouse model of tuberous sclerosis
Ehninger, D., Han, S., Shilyansky, C., Zhou, Y., Li, W., Kwiatkowski, D. J., Ramesh, V., & Silva, A. J. (2008) · Nature Medicine · doi:10.1038/nm1788 · Cited by 879 · see citing works
Self-citationThe heme synthesis and degradation pathways: role in oxidant sensitivity
Ryter, S. W., & Tyrrell, R. M. (2000) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(99)00223-3 · Cited by 822 · see citing works
Mitochondrial Dysfunction in Neurodegenerative Diseases
Johri, A., & Beal, M. F. (2012) · The Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.112.192138 · Cited by 806 · see citing works
Ma, Y., Brewer, J. W., Diehl, J. A., & Hendershot, L. M. (2002) · Journal of Molecular Biology · doi:10.1016/s0022-2836(02)00234-6 · Cited by 689 · see citing works
Rapamycin prevents epilepsy in a mouse model of tuberous sclerosis complex.
Zeng, L., Xu, L., Gutmann, D. H., & Wong, M. (2008) · Annals of Neurology · doi:10.1002/ana.21331 · Cited by 639 · see citing works
Degradation of Misfolded Proteins Prevents ER-Derived Oxidative Stress and Cell Death
Haynes, C. M., Titus, E. A., & Cooper, A. A. (2004) · Molecular Cell · doi:10.1016/j.molcel.2004.08.025 · Cited by 627 · see citing works
Mitochondrial dysfunction in neurodegenerative diseases
Beal, M. F. (1998) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/s0005-2728(98)00114-5 · Cited by 608 · see citing works
Zhang, K., & Kaufman, R. J. (2006) · Neurology · doi:10.1212/01.wnl.0000192306.98198.ec · Cited by 580 · see citing works
Activity-Dependent Regulation of MEF2 Transcription Factors Suppresses Excitatory Synapse Number
Flavell, S. W., Cowan, C. W., Kim, T.-K., Greer, P. L., Lin, Y., Paradis, S., Griffith, E. C., Hu, L. S., Chen, C., & Greenberg, M. E. (2006) · Science · doi:10.1126/science.1122511 · Cited by 573 · see citing works
Coupling Endoplasmic Reticulum Stress to the Cell Death Program
Rao, R. V., Hermel, E., Castro‐Obregón, S., del Rio, G., Ellerby, L., Ellerby, H. M., & Bredesen, D. E. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m102225200 · Cited by 570 · see citing works
Zhuo, M., Small, S. A., Kandel, E. R., & Hawkins, R. D. (1993) · Science · doi:10.1126/science.8100368 · Cited by 553 · see citing works
Meikle, L. M., Pollizzi, K. N., Egnor, A., Kramvis, I., Lane, H. A., Şahin, M., & Kwiatkowski, D. J. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0955-08.2008 · Cited by 500 · see citing works
Self-citationRegulation of neuronal morphology and function by the tumor suppressors Tsc1 and Tsc2
Tavazoie, S. F., Alvarez, V. A., Ridenour, D. A., Kwiatkowski, D. J., & Sabatini, B. L. (2005) · Nature Neuroscience · doi:10.1038/nn1566 · Cited by 497 · see citing works
Self-citationFawcett, T. W., Martindale, J. L., Guyton, K. Z., Hai, T., & Holbrook, N. J. (1999) · Biochemical Journal · doi:10.1042/bj3390135 · Cited by 472 · see citing works
Meikle, L., Talos, D. M., Onda, H., Pollizzi, K., Rotenberg, A., Sahin, M., Jensen, F. E., & Kwiatkowski, D. J. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5540-06.2007 · Cited by 462 · see citing works
Self-citationOxidative stress and the pathogenesis of neurodegenerative disorders.
Reynolds, A. D., Laurie, C., Mosley, R., & Gendelman, H. (2007) · International review of neurobiology · doi:10.1016/s0074-7742(07)82016-2 · Cited by 443 · see citing works
Oxidative stress and mitochondrial dysfunction in neurodegenerative diseases
Trushina, E. V., & McMurray, C. T. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2006.10.056 · Cited by 440 · see citing works
Requirement for Superoxide in Excitotoxic Cell Death
Patel, M., Day, B. J., Crapo, J. D., Fridovich, I., & McNamara, J. O. (1996) · Neuron · doi:10.1016/s0896-6273(00)80052-5 · Cited by 436 · see citing works
Özcan, U., Özcan, L., Yılmaz, E., Düvel, K., Şahin, M., Manning, B. D., & Hotamışlıgil, G. S. (2008) · Molecular Cell · doi:10.1016/j.molcel.2007.12.023 · Cited by 434 · see citing works
Liu, C. Y., Schröder, M., & Kaufman, R. J. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m004454200 · Cited by 421 · see citing works
Tuberous sclerosis: a GAP at the crossroads of multiple signaling pathways
Kwiatkowski, D. J., & Manning, B. D. (2005) · Human Molecular Genetics · doi:10.1093/hmg/ddi260 · Cited by 395 · see citing works
Self-citationLi, M., Baumeister, P., Roy, B., Phan, T., Foti, D. M., Luo, S. D., & Lee, A. S. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.14.5096-5106.2000 · Cited by 368 · see citing works
Dorner, A. J., Wasley, L. C., & Kaufman, R. J. (1992) · The EMBO Journal · doi:10.1002/j.1460-2075.1992.tb05201.x · Cited by 342 · see citing works
Hu, P., Han, Z., Couvillon, A. D., & Exton, J. H. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m407700200 · Cited by 318 · see citing works
Sokka, A.-L., Putkonen, N., Mudò, G., Pryazhnikov, E., Reijonen, S., Khiroug, L. S., Belluardo, N., Lindholm, D., & Korhonen, L. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.4289-06.2007 · Cited by 311 · see citing works
S6K1 Regulates GSK3 under Conditions of mTOR-Dependent Feedback Inhibition of Akt
Zhang, H. H., Lipovsky, A. I., Dibble, C. C., Şahin, M., & Manning, B. D. (2006) · Molecular Cell · doi:10.1016/j.molcel.2006.09.019 · Cited by 309 · see citing works
Identification of novel stress‐induced genes downstream of chop
Wang, X., Kuroda, M., Sok, J., Batchvarova, N., Kimmel, R. A., Chung, P., Zinszner, H., & Ron, D. (1998) · The EMBO Journal · doi:10.1093/emboj/17.13.3619 · Cited by 307 · see citing works
Ero1 and redox homeostasis in the endoplasmic reticulum
Sevier, C. S., & Kaiser, C. A. (2007) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2007.12.011 · Cited by 305 · see citing works
Neural roles for heme oxygenase: Contrasts to nitric oxide synthase
Barañano, D. E., & Snyder, S. H. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.191351298 · Cited by 293 · see citing works
Reversal of long-term potentiation by inhibitors of haem oxygenase
Stevens, C. F., & Wang, Y. (1993) · Nature · doi:10.1038/364147a0 · Cited by 262 · see citing works
Tuberous sclerosis complex proteins control axon formationPreprint
Choi, Y.-J., Nardo, A. D., Kramvis, I., Meikle, L. M., Kwiatkowski, D. J., Şahin, M., & He, X. (2008) · Genes & Development · doi:10.1101/gad.1685008 · Cited by 258 · see citing works
Self-citationmTOR cascade activation distinguishes tubers from focal cortical dysplasia
Baybis, M., Yu, J., Lee, A., Golden, J. A., Weiner, H. L., McKhann, G. M., Aronica, E., & Crino, P. B. (2004) · Annals of Neurology · doi:10.1002/ana.20211 · Cited by 255 · see citing works
Eph-Dependent Tyrosine Phosphorylation of Ephexin1 Modulates Growth Cone Collapse
Şahin, M., Greer, P. L., Lin, M. Z., Poucher, H. K., Eberhart, J. K., Schmidt, S., Wright, T. M., Shamah, S. M., O’Connell, S., Cowan, C. W., et al. (2005) · Neuron · doi:10.1016/j.neuron.2005.01.030 · Cited by 243 · see citing works
Heme oxygenase expression in human central nervous system disorders
Schipper, H. M. (2004) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2004.09.015 · Cited by 237 · see citing works
ER Stress, Hypoxia Tolerance and Tumor Progression
Koumenis, C. (2006) · Current Molecular Medicine · doi:10.2174/156652406775574604 · Cited by 231 · cited 1× · see citing works
“Because many extrinsic factors such as hypoxia, hypoglycemia, and exposure to natural and experimental toxins can lead to ER stress (Koumenis, 2006; Zhang and Kaufman, 2006), Tscdeficient neurons are more likely to be vulnerable to such insults.”
BackgroundYokouchi, M., Hiramatsu, N., Hayakawa, K., Okamura, M., Du, S., Kasai, A., Takano, Y., Shitamura, A., Shimada, T., Yao, J. Q., et al. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m705951200 · Cited by 194 · see citing works
Heme Oxygenase-1: A Novel Therapeutic Target in Oxidative Tissue Injuries
Takahashi, T., Morita, K., Akagi, R., & Sassa, S. (2004) · Current Medicinal Chemistry · doi:10.2174/0929867043365080 · Cited by 192 · see citing works
Endoplasmic reticulum stress and apoptosis
Faitová, J., Krekac, D., Hrstka, R., & Vojtěšek, B. (2006) · Cellular & Molecular Biology Letters · doi:10.2478/s11658-006-0040-4 · Cited by 175 · see citing works
Oxidative Stress, Mitochondrial Dysfunction, and Epilepsy
Patel, M. N. (2002) · Free Radical Research · doi:10.1080/1071576021000016391 · Cited by 152 · see citing works
Mostoslavsky, G., Kotton, D. N., Fabian, A., Gray, J., Lee, J.-S., & Mulligan, R. (2005) · Molecular Therapy · doi:10.1016/j.ymthe.2005.01.005 · Cited by 147 · see citing works
Verkhratsky, A., & Petersen, O. H. (2002) · European Journal of Pharmacology · doi:10.1016/s0014-2999(02)01838-1 · Cited by 143 · see citing works
Orchestrating the unfolded protein response in health and disease
Kaufman, R. J. (2002) · Journal of Clinical Investigation · doi:10.1172/jci200216886 · Cited by 130 · see citing works
Structure and Intermolecular Interactions of the Luminal Dimerization Domain of Human IRE1α
Liu, C. Y., Xu, Z., & Kaufman, R. J. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m300418200 · Cited by 118 · see citing works
Heme Oxygenase‐1: Transducer of Pathological Brain Iron Sequestration under Oxidative Stress
Schipper, H. M. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1306.007 · Cited by 117 · see citing works
Akt up- and down-regulation in response to endoplasmic reticulum stress
Hosoi, T., Hyoda, K., Okuma, Y., Nomura, Y., & Ozawa, K. (2007) · Brain Research · doi:10.1016/j.brainres.2007.03.052 · Cited by 91 · see citing works
Hirose, S. (2006) · Epilepsy Research · doi:10.1016/j.eplepsyres.2005.12.007 · Cited by 82 · see citing works
Endoplasmic Reticulum Stress and Apoptosis Signaling in Human Temporal Lobe Epilepsy
Yamamoto, A., Murphy, N., Schindler, C. K., So, N. K., Stöhr, S., Taki, W., Prehn, J. H. M., & Henshall, D. C. (2006) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/01.jnen.0000202886.22082.2a · Cited by 82 · see citing works
Analysis of mitochondrial free radical generation in animal models of neuronal disease
Kim, D. Y., Won, S. J., & Gwag, B. J. (2002) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(02)00968-1 · Cited by 35 · see citing works
Finlay, G. A., Thannickal, V. J., Fanburg, B. L., & Kwiatkowski, D. J. (2005) · Cancer Research · doi:10.1158/0008-5472.can-05-1394 · Cited by 25 · see citing works
Self-citationLurton, D., Yacubian, E. M. T., Garrido-Sanabria, E. R., da Silva, A. V., Vianna, R., Garzón, E., Sakamoto, A. C., Spreafico, R., & Cavalheiro, É. A. (2002) · Epilepsia · doi:10.1046/j.1528-1157.43.s.5.42.x · Cited by 17 · see citing works
Flagged first, then by citations
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Sorted by citations
Regulation of the mTOR Complex 1 Pathway by Nutrients, Growth Factors, and Stress
Sengupta, S., Peterson, T. R., & Sabatini, D. M. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.09.026 · Cited by 1,234 · see citing works
Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice
Tsai, P. T., Hull, C., Chu, Y., Greene-Colozzi, E., Sadowski, A. R., Leech, J. M., Steinberg, J., Crawley, J. N., Regehr, W. G., & Sahin, M. (2012) · Nature · doi:10.1038/nature11310 · Cited by 888 · see citing works
Self-citationER stress: Autophagy induction, inhibition and selection
Rashid, H.-O., Yadav, R. K., Kim, H., & Chae, H. (2015) · Autophagy · doi:10.1080/15548627.2015.1091141 · Cited by 796 · see citing works
ER stress negatively regulates AKT/TSC/mTOR pathway to enhance autophagy
Qin, L., Wang, Z., Tao, L., & Wang, Y. (2010) · Autophagy · doi:10.4161/auto.6.2.11062 · Cited by 435 · see citing works
Systemic Elevation of PTEN Induces a Tumor-Suppressive Metabolic State
Garcı́a-Cao, I., Song, M. S., Hobbs, R. M., Laurent, G., Giorgi, C., de Boer, V. C. J., Anastasiou, D., Ito, K., Sasaki, A. T., Rameh, L. E., et al. (2012) · Cell · doi:10.1016/j.cell.2012.02.030 · Cited by 403 · see citing works
Molecular neurobiology of mTOR
Switon, K., Kotulska, K., Janusz, A., Zmorzyńska, J., & Jaworski, J. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.11.017 · Cited by 390 · see citing works
Bidirectional crosstalk between endoplasmic reticulum stress and mTOR signaling
Appenzeller‐Herzog, C., & Hall, M. N. (2012) · Trends in Cell Biology · doi:10.1016/j.tcb.2012.02.006 · Cited by 316 · see citing works
Hurst, C. D., Alder, O., Platt, F. M., Droop, A., Stead, L. F., Burns, J. E., Burghel, G. J., Jain, S., Klimczak, L. J., Lindsay, H. A., et al. (2017) · Cancer Cell · doi:10.1016/j.ccell.2017.08.005 · Cited by 307 · see citing works
Tsc2-Rheb signaling regulates EphA-mediated axon guidance
Nie, D. A., Nardo, A. D., Han, J. M., Baharanyi, H., Kramvis, I., Huynh, T., Dabora, S. L., Codeluppi, S., Pandolfi, P. P., Pasquale, E. B., et al. (2010) · Nature Neuroscience · doi:10.1038/nn.2477 · Cited by 243 · see citing works
Self-citationSelvaraj, S., Sun, Y., Watt, J. A., Wang, S., Lei, S., Birnbaumer, L., & Singh, B. B. (2012) · Journal of Clinical Investigation · doi:10.1172/jci61332 · Cited by 245 · see citing works
Tsc1 (hamartin) confers neuroprotection against ischemia by inducing autophagy
Papadakis, M., Hadley, G., Xilouri, M., Hoyte, L. C., Nagel, S., McMenamin, M. M., Tsaknakis, G., Watt, S. M., Drakesmith, C. W., Chen, R., et al. (2013) · Nature Medicine · doi:10.1038/nm.3097 · Cited by 232 · see citing works
Regulation of podocyte survival and endoplasmic reticulum stress by fatty acids
Sieber, J., Lindenmeyer, M. T., Kampe, K., Campbell, K. N., Cohen, C. D., Hopfer, H., Mundel, P., & Jehle, A. W. (2010) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00196.2010 · Cited by 203 · see citing works
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Joo, J. H., Wang, B., Frankel, E. B., Ge, L., Xu, L., Iyengar, R. V., Li-Harms, X., Wright, C., Shaw, T. I., Lindsten, T., et al. (2016) · Molecular Cell · doi:10.1016/j.molcel.2016.04.020 · Cited by 182 · see citing works
Chronic Activation of mTOR Complex 1 Is Sufficient to Cause Hepatocellular Carcinoma in Mice
Menon, S., Yecies, J. L., Zhang, H., Howell, J. J., Nicholatos, J. W., Harputlugil, E., Bronson, R. T., Kwiatkowski, D. J., & Manning, B. D. (2012) · Science Signaling · doi:10.1126/scisignal.2002739 · Cited by 183 · see citing works
Self-citationBridges between mitochondrial oxidative stress, ER stress and mTOR signaling in pancreatic β cells
Wang, J., Yang, X., & Zhang, J. (2016) · Cellular Signalling · doi:10.1016/j.cellsig.2016.05.007 · Cited by 178 · see citing works
Goto, J., Talos, D. M., Klein, P., Qin, W., Chekaluk, Y. I., Anderl, S., Malinowska, I. A., Nardo, A. D., Bronson, R. T., Chan, J. A.-W., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1106454108 · Cited by 179 · see citing works
Self-citationSMN regulates axonal local translation via miR-183/mTOR pathway
Kye, M. J., Niederst, E. D., Wertz, M. H., Gonçalves, I. D. C. G., Akten, B., Dover, K. Z., Peters, M., Rießland, M., Neveu, P. A., Wirth, B., et al. (2014) · Human Molecular Genetics · doi:10.1093/hmg/ddu350 · Cited by 157 · see citing works
McMahon, J. J., Huang, X., Yang, J., Komatsu, M., Yue, Z., Qian, J., Zhu, X. C., & Huang, Y. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.2392-12.2012 · Cited by 154 · see citing works
Gourmaud, S., Shou, H., Irwin, D. J., Sansalone, K., Jacobs, L. M., Lucas, T. H., Marsh, E. D., Davis, K. A., Jensen, F. E., & Talos, D. M. (2020) · Brain · doi:10.1093/brain/awz381 · Cited by 155 · see citing works
PtdIns3P controls mTORC1 signaling through lysosomal positioning
Hong, Z., Pedersen, N. M., Wang, L., Torgersen, M. L., Stenmark, H., & Raiborg, C. (2017) · The Journal of Cell Biology · doi:10.1083/jcb.201611073 · Cited by 154 · see citing works
Mammalian Target of Rapamycin: Hitting the Bull′s‐Eye for Neurological Disorders
Chong, Z. Z., Shang, Y., Zhang, L., Wang, S., & Maiese, K. (2010) · Oxidative Medicine and Cellular Longevity · doi:10.4161/oxim.3.6.14787 · Cited by 149 · see citing works
Impaired Mitochondrial Dynamics and Mitophagy in Neuronal Models of Tuberous Sclerosis Complex
Ebrahimi-Fakhari, D., Saffari, A., Wahlster, L., Di Nardo, A., Turner, D., Lewis, T. L., Conrad, C., Rothberg, J. M., Lipton, J. O., Kölker, S., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.09.054 · Cited by 146 · see citing works
Renal disease in tuberous sclerosis complex: pathogenesis and therapy
Lam, H. C., Siroky, B. J., & Henske, E. P. (2018) · Nature Reviews Nephrology · doi:10.1038/s41581-018-0059-6 · Cited by 132 · see citing works
Targeting PI3K-AKT/mTOR signaling in the prevention of autism
Sharma, A., & Mehan, S. (2021) · Neurochemistry International · doi:10.1016/j.neuint.2021.105067 · Cited by 131 · see citing works
Shedding new light on neurodegenerative diseases through the mammalian target of rapamycin
Chong, Z. Z., Shang, Y. C., Wang, S., & Maiese, K. (2012) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2012.08.001 · Cited by 119 · see citing works
Kang, Y. J., Lü, M., & Guan, K.-L. (2010) · Cell Death and Differentiation · doi:10.1038/cdd.2010.82 · Cited by 115 · see citing works
Neuronal Tsc1/2 complex controls autophagy through AMPK-dependent regulation of ULK1
Nardo, A. D., Wertz, M. H., Kwiatkowski, E. R., Tsai, P. T., Leech, J. D., Greene-Colozzi, E. A., Goto, J., Dilsiz, P., Talos, D. M., Clish, C. B., et al. (2014) · Human Molecular Genetics · doi:10.1093/hmg/ddu101 · Cited by 109 · see citing works
Self-citationTSC1/TSC2 signaling in the CNS
Han, J. M., & Sahin, M. (2011) · FEBS Letters · doi:10.1016/j.febslet.2011.02.001 · Cited by 105 · see citing works
Polman, J. A. E., Hunter, R. G., Speksnijder, N., van den Oever, J. M. E., Korobko, O. B., McEwen, B. S., de Kloet, E. R., & Datson, N. A. (2012) · Endocrinology · doi:10.1210/en.2012-1255 · Cited by 100 · see citing works
Neuronal CTGF/CCN2 negatively regulates myelination in a mouse model of tuberous sclerosis complex
Ercan-Herbst, E., Han, J. M., Nardo, A. D., Winden, K. D., Han, M., Hoyo, L., Saffari, A., Leask, A., Geschwind, D. H., & Şahin, M. (2017) · The Journal of Experimental Medicine · doi:10.1084/jem.20160446 · Cited by 99 · see citing works
Molecular mechanisms of mTOR regulation by stress
Heberle, A. M., Prentzell, M. T., van Eunen, K., Bakker, B. M., Grellscheid, S. N., & Thedieck, K. (2014) · Molecular & Cellular Oncology · doi:10.4161/23723548.2014.970489 · Cited by 97 · see citing works
Fujita, E., Dai, H., Tanabe, Y., Zhiling, Y., Yamagata, T., Miyakawa, T., Tanokura, M., Momoi, M. Y., & Momoi, T. (2010) · Cell Death and Disease · doi:10.1038/cddis.2010.23 · Cited by 90 · see citing works
Arena, A., Zimmer, T., van Scheppingen, J., Korotkov, A., Anink, J., Mühlebner, A., Jansen, F., van Hecke, W., Spliet, W., van Rijen, P. V., et al. (2018) · Brain Pathology · doi:10.1111/bpa.12661 · Cited by 83 · see citing works
Non‐canonical functions of the tuberous sclerosis complex‐Rheb signalling axis
Neuman, N. A., & Henske, E. P. (2011) · EMBO Molecular Medicine · doi:10.1002/emmm.201100131 · Cited by 84 · see citing works
Therapeutic role of mammalian target of rapamycin (mTOR) inhibition in preventing epileptogenesis
McDaniel, S., & Wong, M. (2011) · Neuroscience Letters · doi:10.1016/j.neulet.2011.02.037 · Cited by 78 · see citing works
PRAS40 Is an Integral Regulatory Component of Erythropoietin mTOR Signaling and Cytoprotection
Chong, Z. Z., Shang, Y., Wang, S., & Maiese, K. (2012) · PLoS ONE · doi:10.1371/journal.pone.0045456 · Cited by 75 · see citing works
The ER stress regulator Bip mediates cadmium-induced autophagy and neuronal senescence
Wang, T., Yuan, Y., Zou, H., Yang, J., Zhao, S., Ma, Y., Wang, Y., Bian, J., Liu, X., Gu, J., et al. (2016) · Scientific Reports · doi:10.1038/srep38091 · Cited by 72 · see citing works
Hypothalamic lipotoxicity and the metabolic syndrome
de Morentin, P. B. M., Varela, L., Fernø, J., Nogueiras, R., Diéguez, C., & López, M. (2009) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2009.09.016 · Cited by 70 · see citing works
Ehninger, D. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.05.015 · Cited by 68 · see citing works
The Neurodevelopmental Pathogenesis of Tuberous Sclerosis Complex (TSC)
Feliciano, D. M. (2020) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2020.00039 · Cited by 69 · see citing works
Xie, X., Ma, L., Xi, K., Zhang, W., & Fan, D. (2017) · Cellular Physiology and Biochemistry · doi:10.1159/000455987 · Cited by 68 · see citing works
The role of autophagy in endoplasmic reticulum stress-induced pancreatic β cell death
Yin, J.-J., Li, Y., Wang, Y., Liu, G., Wang, J., Zhu, X.-O., & Pan, S. (2012) · Autophagy · doi:10.4161/auto.8.2.18807 · Cited by 65 · see citing works
Loss of the tuberous sclerosis complex protein tuberin causes Purkinje cell degeneration
Reith, R. M., Way, S., McKenna, J., Haines, K., & Gambello, M. J. (2011) · Neurobiology of Disease · doi:10.1016/j.nbd.2011.02.014 · Cited by 65 · see citing works
Lam, H. C., Baglini, C. V., Lope, A. L., Parkhitko, A. A., Liu, H.-J., Alesi, N., Malinowska, I. A., Ebrahimi‐Fakhari, D., Saffari, A., Yu, J. J., et al. (2017) · Cancer Research · doi:10.1158/0008-5472.can-16-2458 · Cited by 61 · see citing works
Chen Shang, Y., Zhong Chong, Z., Wang, S., & Maiese, K. (2013) · Current Neurovascular Research · doi:10.2174/156720213804806007 · Cited by 61 · see citing works
“In other cell systems such as with neurons, neurons without a functional TSC1/TSC2 complex have been shown to have increased vulnerability to endoplasmic reticulum stress-induced cell death through the activation of the mitochondrial death pathway [55].”
BackgroundRedox Characterization of Functioning Skeletal Muscle
Zuo, L., & Pannell, B. K. (2015) · Frontiers in Physiology · doi:10.3389/fphys.2015.00338 · Cited by 60 · see citing works
Purinergic Signaling and Energy Homeostasis in Psychiatric Disorders
Lindberg, D. M., Shan, D., Ayers-Ringler, J. R., Oliveros, A., Benitez, J. C. A., Prieto, M. L., McCullumsmith, R. E., & Choi, D. (2015) · Current Molecular Medicine · doi:10.2174/1566524015666150330163724 · Cited by 59 · see citing works
Activity-Dependent Augmentation of Spontaneous Neurotransmission during Endoplasmic Reticulum Stress
Nosyreva, E. D., & Kavalali, E. T. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5358-09.2010 · Cited by 58 · see citing works
Tuberous Sclerosis: A New Frontier in Targeted Treatment of Autism
Davis, P. E., Peters, J. M., Krueger, D. A., & Şahin, M. (2015) · Neurotherapeutics · doi:10.1007/s13311-015-0359-5 · Cited by 58 · see citing works
Picchioni, D., Reith, R. M., Nadel, J., & Smith, C. B. (2014) · Brain Sciences · doi:10.3390/brainsci4010150 · Cited by 55 · see citing works
EphA7 signaling guides cortical dendritic development and spine maturation
Clifford, M. A., Athar, W., Leonard, C. E., Russo, A., Sampognaro, P. J., van der Goes, M.-S. H., Burton, D. A., Zhao, X., Lalchandani, R. R., Şahin, M., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1323793111 · Cited by 55 · see citing works
TSC1 involvement in bladder cancer: diverse effects and therapeutic implications
Guo, Y., Chekaluk, Y. I., Zhang, J., Du, J., Gray, N. S., Wu, C., & Kwiatkowski, D. J. (2013) · The Journal of Pathology · doi:10.1002/path.4176 · Cited by 52 · see citing works
Self-citationMartinez, T. N., Chen, X., Bandyopadhyay, S., Merrill, A. H., & Tansey, M. G. (2012) · Molecular Neurodegeneration · doi:10.1186/1750-1326-7-45 · Cited by 52 · see citing works
Wu, J., Ma, S., Sandhoff, R., Ming, Y., Hotz‐Wagenblatt, A., Timmerman, V., Bonello‐Palot, N., Schlotter‐Weigel, B., Auer‐Grumbach, M., Seeman, P., et al. (2019) · Immunity · doi:10.1016/j.immuni.2019.03.005 · Cited by 52 · see citing works
Ras Homolog Enriched in Brain (Rheb) Enhances Apoptotic Signaling*
Karassek, S., Berghaus, C., Schwarten, M., Goemans, C. G., Ohse, N., Kock, G., Jockers, K. F. G., Neumann, S., Gottfried, S., Herrmann, C., et al. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.095968 · Cited by 51 · see citing works
mTOR signaling in neural stem cells: from basic biology to disease
Magri, L., & Galli, R. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-1196-x · Cited by 51 · see citing works
Teotia, P., Hook, M. J. V., Fischer, D., & Ahmad, I. (2019) · Development · doi:10.1242/dev.178012 · Cited by 50 · see citing works
Zimmer, T. S., Broekaart, D. W. M., Gruber, V.-E., van Vliet, E. A., Mühlebner, A., & Aronica, E. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.01028 · Cited by 48 · see citing works
The tuberous sclerosis complex: balancing proliferation and survival
Tomasoni, R., & Mondino, A. (2011) · Biochemical Society Transactions · doi:10.1042/bst0390466 · Cited by 46 · see citing works
Nie, D. A., Chen, Z., Ebrahimi‐Fakhari, D., Nardo, A. D., Jülich, K., Robson, V. K., Cheng, Y.-C., Woolf, C. J., Heiman, M., & Şahin, M. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4796-14.2015 · Cited by 45 · see citing works
Mafi, S., Ahmadi, E., Meehan, E. V., Chiari, C. C., Mansoori, B., Sadeghi, H., Milani, S., Jafarinia, M., Taeb, S., Bashmagh, B. M., et al. (2023) · Cancer Research · doi:10.1158/0008-5472.can-22-3032 · Cited by 42 · see citing works
GADD34 mediates cytoprotective autophagy in mutant huntingtin expressing cells via the mTOR pathway
Hyrskyluoto, A., Reijonen, S., Kivinen, J., Lindholm, D., & Korhonen, L. (2011) · Experimental Cell Research · doi:10.1016/j.yexcr.2011.08.020 · Cited by 43 · see citing works
Tuberous sclerosis complex: From molecular biology to novel therapeutic approaches
Switon, K., Kotulska, K., Janusz, A., Zmorzyńska, J., & Jaworski, J. (2016) · IUBMB Life · doi:10.1002/iub.1579 · Cited by 44 · see citing works
Cerebellar Development and Autism Spectrum Disorder in Tuberous Sclerosis Complex
Sundberg, M., & Şahin, M. (2015) · Journal of Child Neurology · doi:10.1177/0883073815600870 · Cited by 42 · see citing works
Babcock, J. T., Nguyen, H., He, Y., Hendricks, J. W., Wek, R. C., & Quilliam, L. A. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.431056 · Cited by 42 · see citing works
Kanngießer, M., Häußler, A., Myrczek, T., Küsener, N., Lim, H., Geißlinger, G., Niederberger, E., & Tegeder, I. (2012) · Journal of Pain · doi:10.1016/j.jpain.2012.02.010 · Cited by 41 · see citing works
Human TSC-associated renal angiomyolipoma cells are hypersensitive to ER stress
Siroky, B. J., Yin, H. J., Babcock, J. T., Lu, L., Hellmann, A. R., Dixon, B. P., Quilliam, L. A., & Bissler, J. J. (2012) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00441.2011 · Cited by 41 · see citing works
The role of the endoplasmic reticulum stress response following cerebral ischemia
Hadley, G., Neuhaus, A. A., Couch, Y., Beard, D. J., Adriaanse, B. A., Vekrellis, K., DeLuca, G. C., Papadakis, M., Sutherland, B. A., & Buchan, A. M. (2017) · International Journal of Stroke · doi:10.1177/1747493017724584 · Cited by 40 · see citing works
Zeng, L. (2009) · Molecular and Cellular Pharmacology · doi:10.4255/mcpharmacol.09.16 · Cited by 39 · see citing works
Johnson, C. E., Hunt, D. K., Wiltshire, M., Herbert, T. P., Sampson, J. R., Errington, R. J., Davies, D. M., & Tee, A. R. (2014) · Molecular Oncology · doi:10.1016/j.molonc.2014.11.005 · Cited by 37 · see citing works
Tripathi, R., Aggarwal, T., Lindberg, F. A., Klemm, A. H., & Fredriksson, R. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.854397 · Cited by 36 · see citing works
Chronic activation of anti‐oxidant pathways and iron accumulation in epileptogenic malformations
Zimmer, T. S., Ciriminna, G., Arena, A., Anink, J. J., Korotkov, A., Jansen, F. E., Hecke, W. V., Spliet, W. G. M., van Rijen, P. C., Baayen, J. C., et al. (2019) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12596 · Cited by 33 · see citing works
Huang, Y., Feng, Y., Wang, Y., Wang, P., Wang, F., & Ren, H. J. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00441 · Cited by 31 · see citing works
Koromilas, A. E., & Mounir, Z. (2013) · Future Oncology · doi:10.2217/fon.13.49 · Cited by 31 · see citing works
Perspectives of RAS and RHEB GTPase Signaling Pathways in Regenerating Brain Neurons
Schöneborn, H., Raudzus, F., Coppey, M., Neumann, S., & Heumann, R. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19124052 · Cited by 30 · see citing works
Guo, T., Dakkak, D., Rodríguez-Martín, T., Noble, W. J., & Hanger, D. P. (2019) · Acta Neuropathologica Communications · doi:10.1186/s40478-018-0651-9 · Cited by 30 · see citing works
A Magnetic Resonance Imaging Study of Cerebellar Volume in Tuberous Sclerosis Complex
Weisenfeld, N., Peters, J. M., Tsai, P. T., Prabhu, S. P., Dies, K. A., Şahin, M., & Warfield, S. K. (2013) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2012.10.011 · Cited by 30 · see citing works
Comparative analysis ofTsc1andTsc2single and double radial glial cell mutants
Mietzsch, U., McKenna, J. T., Reith, R. M., Way, S. W., & Gambello, M. J. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23380 · Cited by 28 · see citing works
Targeting PRAS40 for multiple diseases
Chong, Z. Z. (2016) · Drug Discovery Today · doi:10.1016/j.drudis.2016.04.005 · Cited by 28 · see citing works
mTORC1 Crosstalk With Stress Granules in Aging and Age-Related Diseases
Sandoval, M. C., Heberle, A. M., Rehbein, U., Barile, C., Pittol, J. M. R., & Thedieck, K. (2021) · Frontiers in Aging · doi:10.3389/fragi.2021.761333 · Cited by 27 · see citing works
Opposing effects of monomeric and pentameric C-reactive protein on endothelial progenitor cells
Ahrens, I., Domeij, H., Eisenhardt, S. U., Topcic, D., Albrecht, M., Leitner, E., Viitaniemi, K., Jowett, J. B. M., Lappas, M., Bode, C., et al. (2011) · Basic Research in Cardiology · doi:10.1007/s00395-011-0191-y · Cited by 27 · see citing works
Ras and Rheb Signaling in Survival and Cell Death
Ehrkamp, A., Herrmann, C., Stoll, R., & Heumann, R. (2013) · Cancers · doi:10.3390/cancers5020639 · Cited by 27 · see citing works
Interpreting the Stress Response of Early Mammalian Embryos and Their Stem Cells
Xie, Y., Awonuga, A. O., Zhou, S., Puscheck, E. E., & Rappolee, D. A. (2011) · International review of cytology · doi:10.1016/b978-0-12-386043-9.00002-5 · Cited by 27 · see citing works
Nardo, A. D., Lenoël, I., Winden, K. D., Rühmkorf, A., Modi, M. E., Barrett, L. B., Ercan-Herbst, E., Venugopal, P., Behne, R., Lopes, C. A. M., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107780 · Cited by 26 · see citing works
Zimmer, T. S., Korotkov, A., Zwakenberg, S., Jansen, F. E., Zwartkruis, F. J. T., Rensing, N. R., Wong, M., Mühlebner, A., van Vliet, E. A., Aronica, E., et al. (2021) · Brain Pathology · doi:10.1111/bpa.12949 · Cited by 26 · see citing works
A Critical Period for Development of Cerebellar-Mediated Autism-Relevant Social Behavior
Gibson, J. M., Howland, C. P., Ren, C., Howland, C., Vernino, A., & Tsai, P. T. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1230-21.2021 · Cited by 25 · see citing works
Yuskaitis, C. J., Modasia, J. B., Schrötter, S., Rossitto, L.-A. M., Groff, K. J., Morici, C., Mithal, D., Chakrabarty, R., Chandel, N., Manning, B., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111278 · Cited by 21 · see citing works
Kawada, K., Mimori, S., Okuma, Y., & Nomura, Y. (2017) · Neurochemistry International · doi:10.1016/j.neuint.2017.07.004 · Cited by 25 · see citing works
Deficiency of hepatocystin induces autophagy through an mTOR-dependent pathway
Yang, J. H., Zhao, Y., Ma, K., Jiang, F.-J., Liao, W., Zhang, P., Zhou, J., Tu, B., Wang, L., Kampinga, H. H., et al. (2011) · Autophagy · doi:10.4161/auto.7.7.15822 · Cited by 25 · see citing works
Examination of a second node of translational control in the unfolded protein response
Preston, A. M., & Hendershot, L. M. (2013) · Journal of Cell Science · doi:10.1242/jcs.130336 · Cited by 24 · see citing works
Mitochondrial “Hypermetabolic” Neurons in Paediatric Epileptic Foci
Sarnat, H. B., Flores‐Sarnat, L., Hader, W. J., & Bello‐Espinosa, L. E. (2011) · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · doi:10.1017/s0317167100012518 · Cited by 24 · see citing works
Ablation of PGC1 beta prevents mTOR dependent endoplasmic reticulum stress response
Camacho‐Morales, A., Rodriguez-Cuenca, S., Blount, M., Prieur, X., Barbarroja, N., Fuller, M., Hardingham, G. E., & Vidal‐Puig, A. (2012) · Experimental Neurology · doi:10.1016/j.expneurol.2012.06.031 · Cited by 24 · see citing works
Li, L., Chai, Y., Guo, X., Chu, S., & Zhang, L.-S. (2018) · Molecular Medicine Reports · doi:10.3892/mmr.2018.8840 · Cited by 24 · see citing works
Tuberous sclerosis—A model for tumour growth
Dodd, K. M., & Dunlop, E. A. (2016) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2016.01.025 · Cited by 23 · see citing works
Park, Y., Ko, J., Jang, Y., & Kwon, Y. H. (2013) · Neurochemical Research · doi:10.1007/s11064-013-1057-5 · Cited by 22 · see citing works
Guerra, D. J. (2011) · Autism Research and Treatment · doi:10.1155/2011/398636 · Cited by 22 · see citing works
Venkatesh, A., Ma, S., & Punzo, C. (2016) · Cell Death and Disease · doi:10.1038/cddis.2016.182 · Cited by 20 · see citing works
Mechanisms of sleep and circadian ontogeny through the lens of neurodevelopmental disorders
Barone, I., Hawks-Mayer, H., & Lipton, J. O. (2019) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2019.01.011 · Cited by 21 · see citing works
Stochastic Model of Tsc1 Lesions in Mouse Brain
Prabhakar, S., Goto, J., Zuang, X., Sena‐Esteves, M., Bronson, R. T., Brockmann, J., Gianni, D., Wojtkiewicz, G. R., Chen, J. W., Stemmer-Rachamimov, A. O., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0064224 · Cited by 20 · see citing works
Self-citation
- Authors
- Di Nardo, A., Kramvis, I., Cho, N., Sadowski, A., Meikle, L., Kwiatkowski, D. J., & Sahin, M.
- Affiliations
- Boston Children's Hospital (US)
- Brigham and Women's Hospital (US)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2009-05-06
- Volume
- 29
- Issue
- 18
- Pages
- 5926-5937
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC2691854
- OpenAlex
- W2002327194
- Cited by
- 165
- References
- 69
- Citations by year
- 2026: 3 · 2025: 2 · 2024: 3 · 2023: 4 · 2022: 7 · 2021: 12 · 2020: 6 · 2019: 9 · 2018: 8 · 2017: 10 · 2016: 14 · 2015: 9 · 2014: 10 · 2013: 14 · 2012: 24
- FWCI
- 11.97
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Edinburgh Research Explorer (University of Edinburgh) (submittedVersion, other-oa)
- Funders
- Tuberous Sclerosis Alliance
- Manton Foundation
- National Institutes of Health
- National Institute of Neurological Disorders and Stroke (R01NS058956, P01NS024279)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (P30HD018655)
- Topics
- Health Sciences › Medicine › Physiology › Tuberous Sclerosis Complex Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Endoplasmic Reticulum Stress and Disease
- Keywords
- tuberous sclerosis complex, TSC1, TSC2, mTOR, endoplasmic reticulum stress, oxidative stress, neuronal stress response, CHOP, heme oxygenase-1, mitochondrial apoptosis, ER stress-induced cell death, hippocampal neurons, rapamycin, neurocognitive impairment
- MeSH terms
- Tuberous Sclerosis Complex 1 Protein, Tuberous Sclerosis Complex 2 Protein, Animals, Animals, Newborn, Carrier Proteins, Cells, Cultured, Child, Preschool, Dose-Response Relationship, Drug, Embryo, Mammalian, Endoplasmic Reticulum, Flow Cytometry, Gene Expression Regulation, Hippocampus, Humans, Lactones, Male, Mice, Transgenic, Mitochondria, Neurons, Serine, Sesquiterpenes, Threonine, Time Factors, Transduction, Genetic, Tuberous Sclerosis, Tunicamycin, Apoptosis, Reactive Oxygen Species, Phosphotransferases (Alcohol Group Acceptor), Oxidative Stress, Tumor Suppressor Proteins, RNA, Small Interfering, Mice, Heme Oxygenase-1, Transcription Factor CHOP, TOR Serine-Threonine Kinases
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