Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 4 de 4
Filter
Add more filters










Database
Language
Publication year range
1.
Brain Res ; 1706: 24-31, 2019 03 01.
Article in English | MEDLINE | ID: mdl-30366018

ABSTRACT

DYT1 dystonia is a neurological disease caused by a dominant mutation that results in the loss of a glutamic acid in the endoplasmic reticulum-resident protein torsinA. Currently, treatments are symptomatic and only provide partial relief. Multiple reports support the hypothesis that selectively reducing expression of mutant torsinA without affecting levels of the wild type protein should be beneficial. Published cell-based studies support this hypothesis. It is unclear, however, if phenotypes are reversible by targeting the molecular defect once established in vivo. Here, we generated adeno-associated virus encoding artificial microRNA targeting human mutant torsinA and delivered them to the striatum of symptomatic transgenic rats that express the full human TOR1A mutant gene. We achieved efficient suppression of human mutant torsinA expression in DYT1 transgenic rats, partly reversing its accumulation in the nuclear envelope. This intervention rescued PERK-eIF2α pathway dysregulation in striatal projection neurons but not behavioral abnormalities. Moreover, we found abnormal expression of components of dopaminergic neurotransmission in DYT1 rat striatum, which were not normalized by suppressing mutant torsinA expression. Our findings demonstrate the reversibility of translational dysregulation in DYT1 neurons and confirm the presence of abnormal dopaminergic neurotransmission in DYT1 dystonia.


Subject(s)
Eukaryotic Initiation Factor-2/metabolism , Molecular Chaperones/metabolism , eIF-2 Kinase/metabolism , Animals , Corpus Striatum/metabolism , Dystonia/genetics , Dystonia/therapy , Dystonia Musculorum Deformans/genetics , Dystonia Musculorum Deformans/metabolism , Endoplasmic Reticulum/metabolism , Eukaryotic Initiation Factor-2/physiology , Female , Humans , Interneurons/metabolism , Male , Molecular Chaperones/genetics , Mutation , Neurons/metabolism , RNA Interference/physiology , Rats , Rats, Sprague-Dawley , Rats, Transgenic , Signal Transduction/genetics , eIF-2 Kinase/physiology
2.
Neuroscience ; 371: 455-468, 2018 02 10.
Article in English | MEDLINE | ID: mdl-29289717

ABSTRACT

DYT1 dystonia is a neurological disease caused by dominant mutations in the TOR1A gene, encoding for the endoplasmic reticulum (ER)-resident protein torsinA. Recent reports linked expression of the DYT1-causing protein with dysregulation of eIF2α, a key component of the cellular response to ER stress known as the unfolded protein response (UPR). However, the response of the DYT1 mammalian brain to acute ER stress inducers has not been evaluated in vivo. We hypothesized that torsinA regulates the neuronal UPR and expression of its mutant form would alter this process. TorsinA was post-transcriptionally upregulated upon acute ER stress in different models, suggesting a role in this response. Moreover, increased basal phosphorylation of eIF2α in DYT1 transgenic rats was associated with an abnormal response to acute ER stress. Finally, an unbiased RNA-Seq-based transcriptomic analysis of embryonic brain tissue in heterozygous and homozygous DYT1 knockin mice confirmed the presence of eIF2α dysregulation in the DYT1 brain. In sum, these findings support previous reports linking torsinA function, eIF2α signaling and the neuronal response to ER stress in vivo. Furthermore, we describe novel protocols to investigate neuronal ER stress in cultured neurons and in vivo.


Subject(s)
Brain/metabolism , Dystonia Musculorum Deformans/metabolism , Endoplasmic Reticulum Stress/physiology , Eukaryotic Initiation Factor-2/metabolism , Animals , Brain/drug effects , Brain/embryology , Brain/pathology , Central Nervous System Agents/pharmacology , Dose-Response Relationship, Drug , Endoplasmic Reticulum Stress/drug effects , Female , Humans , Induced Pluripotent Stem Cells/drug effects , Induced Pluripotent Stem Cells/metabolism , Male , Mice, Transgenic , Rats, Sprague-Dawley , Rats, Transgenic , Transcriptome , Tunicamycin/pharmacology , Unfolded Protein Response/drug effects , Unfolded Protein Response/physiology , Up-Regulation
3.
J Neurosci ; 36(40): 10245-10256, 2016 10 05.
Article in English | MEDLINE | ID: mdl-27707963

ABSTRACT

Dystonia type 1 (DYT1) is a dominantly inherited neurological disease caused by mutations in TOR1A, the gene encoding the endoplasmic reticulum (ER)-resident protein torsinA. Previous work mostly completed in cell-based systems suggests that mutant torsinA alters protein processing in the secretory pathway. We hypothesized that inducing ER stress in the mammalian brain in vivo would trigger or exacerbate mutant torsinA-induced dysfunction. To test this hypothesis, we crossed DYT1 knock-in with p58(IPK)-null mice. The ER co-chaperone p58(IPK) interacts with BiP and assists in protein maturation by helping to fold ER cargo. Its deletion increases the cellular sensitivity to ER stress. We found a lower generation of DYT1 knock-in/p58 knock-out mice than expected from this cross, suggesting a developmental interaction that influences viability. However, surviving animals did not exhibit abnormal motor function. Analysis of brain tissue uncovered dysregulation of eiF2α and Akt/mTOR translational control pathways in the DYT1 brain, a finding confirmed in a second rodent model and in human brain. Finally, an unbiased proteomic analysis identified relevant changes in the neuronal protein landscape suggesting abnormal ER protein metabolism and calcium dysregulation. Functional studies confirmed the interaction between the DYT1 genotype and neuronal calcium dynamics. Overall, these findings advance our knowledge on dystonia, linking translational control pathways and calcium physiology to dystonia pathogenesis and identifying potential new pharmacological targets. SIGNIFICANCE STATEMENT: Dystonia type 1 (DYT1) is one of the different forms of inherited dystonia, a neurological disorder characterized by involuntary, disabling movements. DYT1 is caused by mutations in the gene that encodes the endoplasmic reticulum (ER)-resident protein torsinA. How mutant torsinA causes neuronal dysfunction remains unknown. Here, we show the behavioral and molecular consequences of stressing the ER in DYT1 mice by increasing the amount of misfolded proteins. This resulted in the generation of a reduced number of animals, evidence of abnormal ER protein processing and dysregulation of translational control pathways. The work described here proposes a shared mechanism for different forms of dystonia, links for the first time known biological pathways to dystonia pathogenesis, and uncovers potential pharmacological targets for its treatment.


Subject(s)
Dystonia/genetics , Dystonia/physiopathology , Endoplasmic Reticulum/genetics , Molecular Chaperones/genetics , Animals , Behavior, Animal , Calcium Signaling/genetics , Cerebellum/physiopathology , Dystonia/psychology , Endoplasmic Reticulum Stress/genetics , Gene Expression Regulation/genetics , Gene Knock-In Techniques , Genotype , HSP40 Heat-Shock Proteins/genetics , HSP40 Heat-Shock Proteins/metabolism , Humans , Mice , Mice, Knockout , Neurons/physiology , Signal Transduction/genetics
4.
PLoS One ; 9(9): e109099, 2014.
Article in English | MEDLINE | ID: mdl-25268642

ABSTRACT

In humans, sensory abnormalities, including neuropathic pain, often result from traumatic spinal cord injury (SCI). SCI can induce cellular changes in the CNS, termed central sensitization, that alter excitability of spinal cord neurons, including those in the dorsal horn involved in pain transmission. Persistently elevated levels of neuronal activity, glial activation, and glutamatergic transmission are thought to contribute to the hyperexcitability of these dorsal horn neurons, which can lead to maladaptive circuitry, aberrant pain processing and, ultimately, chronic neuropathic pain. Here we present a mouse model of SCI-induced neuropathic pain that exhibits a persistent pain phenotype accompanied by chronic neuronal hyperexcitability and glial activation in the spinal cord dorsal horn. We generated a unilateral cervical contusion injury at the C5 or C6 level of the adult mouse spinal cord. Following injury, an increase in the number of neurons expressing ΔFosB (a marker of chronic neuronal activation), persistent astrocyte activation and proliferation (as measured by GFAP and Ki67 expression), and a decrease in the expression of the astrocyte glutamate transporter GLT1 are observed in the ipsilateral superficial dorsal horn of cervical spinal cord. These changes have previously been associated with neuronal hyperexcitability and may contribute to altered pain transmission and chronic neuropathic pain. In our model, they are accompanied by robust at-level hyperaglesia in the ipsilateral forepaw and allodynia in both forepaws that are evident within two weeks following injury and persist for at least six weeks. Furthermore, the pain phenotype occurs in the absence of alterations in forelimb grip strength, suggesting that it represents sensory and not motor abnormalities. Given the importance of transgenic mouse technology, this clinically-relevant model provides a resource that can be used to study the molecular mechanisms contributing to neuropathic pain following SCI and to identify potential therapeutic targets for the treatment of chronic pathological pain.


Subject(s)
Contusions/physiopathology , Hyperalgesia/physiopathology , Neuralgia/physiopathology , Spinal Cord Dorsal Horn/physiopathology , Spinal Cord Injuries/physiopathology , Animals , Astrocytes/metabolism , Astrocytes/pathology , Biomarkers/metabolism , Cell Proliferation , Contusions/complications , Contusions/metabolism , Disease Models, Animal , Excitatory Amino Acid Transporter 2/genetics , Excitatory Amino Acid Transporter 2/metabolism , Gene Expression , Glial Fibrillary Acidic Protein , Hyperalgesia/complications , Hyperalgesia/metabolism , Ki-67 Antigen/genetics , Ki-67 Antigen/metabolism , Male , Mice , Mice, Inbred C57BL , Mice, Transgenic , Nerve Tissue Proteins/genetics , Nerve Tissue Proteins/metabolism , Neuralgia/complications , Neuralgia/metabolism , Neurons/metabolism , Neurons/pathology , Proto-Oncogene Proteins c-fos/genetics , Proto-Oncogene Proteins c-fos/metabolism , Spinal Cord Dorsal Horn/injuries , Spinal Cord Dorsal Horn/metabolism , Spinal Cord Injuries/complications , Spinal Cord Injuries/metabolism
SELECTION OF CITATIONS
SEARCH DETAIL
...