Sigma-1 receptor (Sig-1R) functions as a chaperon that interacts with multiple proteins and lipids and is implicated in neurodegenerative and psychiatric diseases. This year in a collaboration with Dr. Bonci's lab we found that vesicular glutamate transporters in dopamine neurons play a critical role in neuroprotection against MPTP-induced Parkinsonism in a rat model. Specifically, genetic deletion of the vesicular glutamate transporter enhances the neurotoxicity of MPTP. Although the sigma-1 receptor was not examined in this study, we feel that the result of this study may have a bearing with the sigma-1 receptor because the sigma-1 receptor has been shown to protect against Parkinsonism. In another study on neuroprotection, we found that Sp1 was highly expressed in astrocytes, implying that Sp1 might be important for the function of astrocytes. Sp1/GFAP-Cre-ERT2 conditional knockout mice were constructed to study the role of Sp1 in astrocytes. Knockout of Sp1 in astrocytes altered astrocytic morphology and decreased GFAP expression in the cortex and hippocampus but did not affect cell viability. Loss of Sp1 in astrocytes decreased the number of neurons in the cortex and hippocampus. Conditioned medium from primary astrocytes with Sp1 knockout disrupted neuronal dendritic outgrowth and synapse formation, resulting in abnormal learning, memory, and motor behavior. Sp1 knockout in astrocytes altered gene expression, including decreasing the expression of Toll-like receptor 2 and Cfb and increasing the expression of C1q and C4Bp, thereby affecting neurite outgrowth and synapse formation, resulting in disordered neuron function. Studying these gene regulations might be beneficial to understanding neuronal development and brain injury prevention. Since the sigma-1 receptor can affect chromatin remodeling via an interaction with the nuclear envelope protein, future investigation on the potential interaction of sigma-1 receptor and Sp1 may advance our understanding on the transcriptional regulation of sigma-1 receptor.

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Budget End
Support Year
11
Fiscal Year
2019
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Name
National Institute on Drug Abuse
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Tsai, Shang-Yi Anne; Su, Tsung-Ping (2017) Sigma-1 Receptors Fine-Tune the Neuronal Networks. Adv Exp Med Biol 964:79-83
Weng, Tzu-Yu; Hung, Denise T; Su, Tsung-Ping et al. (2017) Loss of Sigma-1 Receptor Chaperone Promotes Astrocytosis and Enhances the Nrf2 Antioxidant Defense. Oxid Med Cell Longev 2017:4582135
Chuang, Jian-Ying; Kao, Tzu-Jen; Lin, Shu-Hui et al. (2017) Specificity protein 1-zinc finger protein 179 pathway is involved in the attenuation of oxidative stress following brain injury. Redox Biol 11:135-143
Williams, Abasha; Hayashi, Teruo; Wolozny, Daniel et al. (2016) The non-apoptotic action of Bcl-xL: regulating Ca(2+) signaling and bioenergetics at the ER-mitochondrion interface. J Bioenerg Biomembr 48:211-25
Su, Tzu-Chieh; Lin, Shu-Hui; Lee, Pin-Tse et al. (2016) The sigma-1 receptor-zinc finger protein 179 pathway protects against hydrogen peroxide-induced cell injury. Neuropharmacology 105:1-9
Ciesielski, Jenna; Su, Tsung-Ping; Tsai, Shang-Yi (2016) Myristic acid hitchhiking on sigma-1 receptor to fend off neurodegeneration. Receptors Clin Investig 3:
Tsai, Shang-Yi A; Pokrass, Michael J; Klauer, Neal R et al. (2015) Sigma-1 receptor regulates Tau phosphorylation and axon extension by shaping p35 turnover via myristic acid. Proc Natl Acad Sci U S A 112:6742-7
Lewis, Abasha; Hayashi, Teruo; Su, Tsung-Ping et al. (2014) Bcl-2 family in inter-organelle modulation of calcium signaling; roles in bioenergetics and cell survival. J Bioenerg Biomembr 46:1-15
Fujimoto, Michiko; Hayashi, Teruo; Su, Tsung-Ping (2012) The role of cholesterol in the association of endoplasmic reticulum membranes with mitochondria. Biochem Biophys Res Commun 417:635-9
Fujimoto, Michiko; Hayashi, Teruo; Urfer, Roman et al. (2012) Sigma-1 receptor chaperones regulate the secretion of brain-derived neurotrophic factor. Synapse 66:630-9

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