keyword
https://read.qxmd.com/read/34247243/the-orphan-gpcr-receptor-gpr88-interacts-with-nuclear-protein-partners-in-the-cerebral-cortex
#21
JOURNAL ARTICLE
Florian Rebeillard, Stéphanie De Gois, Nicolas Pietrancosta, Thi Hue Mai, René Lai-Kuen, Brigitte L Kieffer, Bruno Giros, Renaud Massart, Michèle Darmon, Jorge Diaz
GPR88 is an orphan G-protein-coupled receptor (GPCR) highly expressed in striatal medium spiny neurons (MSN), also found in cortical neurons at low level. In MSN, GPR88 has a canonical GPCR plasma membrane/cytoplasmic expression, whereas in cortical neurons, we previously reported an atypical intranuclear localization. Molecular size analysis suggests that GPR88, expressed in plasma membrane of MSN or in nuclear compartment of cortical neurons, corresponds to the full-length protein. By transfection of cortical neurons, we showed that GPR88 fluorescent chimeras exhibit a nuclear localization...
July 9, 2021: Cerebral Cortex
https://read.qxmd.com/read/34187517/cocaine-induced-neuron-subtype-mitochondrial-dynamics-through-egr3-transcriptional-regulation
#22
JOURNAL ARTICLE
Shannon L Cole, Ramesh Chandra, Maya Harris, Ishan Patel, Torrance Wang, Hyunjae Kim, Leah Jensen, Scott J Russo, Gustavo Turecki, Amy M Gancarz-Kausch, David M Dietz, Mary Kay Lobo
Mitochondrial function is required for brain energy homeostasis and neuroadaptation. Recent studies demonstrate that cocaine affects mitochondrial dynamics and morphological characteristics within the nucleus accumbens (NAc). Further, mitochondria are differentially regulated by cocaine in dopamine receptor-1 containing medium spiny neurons (D1-MSNs) vs dopamine receptor-2 (D2)-MSNs. However, there is little understanding into cocaine-induced transcriptional mechanisms and their role in regulating mitochondrial processes...
June 29, 2021: Molecular Brain
https://read.qxmd.com/read/34029288/ninjin-yoeito-a-traditional-japanese-kampo-medicine-suppresses-the-onset-of-anhedonia-induced-by-dysfunction-in-the-striatal-dopamine-receptor-type-2-expressing-medium-spiny-neurons
#23
JOURNAL ARTICLE
Hiroaki Oizumi, Ryota Imai, Toru Suzuki, Yuji Omiya, Kenji F Tanaka, Masaru Mimura, Kazushige Mizoguchi
OBJECTIVE: Recent studies have suggested that ninjin'yoeito (NYT), a traditional Japanese Kampo medicine, improves diminished motivation in humans and animals, rendering it a novel therapeutic option for impaired motivation. To better characterize the effect of NYT on motivation, we examined its effect on motivated behaviors in mice. METHODS: Mouse models of neurodegeneration-related apathy, in which striatal dopamine receptor type 2-expressing medium spiny neurons (D2-MSNs) were progressively damaged by diphtheria toxin expression, were chosen...
May 20, 2021: Neuroreport
https://read.qxmd.com/read/33771089/modulation-of-setdb1-activity-by-apq-ameliorates-heterochromatin-condensation-motor-function-and-neuropathology-in-a-huntington-s-disease-mouse-model
#24
JOURNAL ARTICLE
Yu Jin Hwang, Seung Jae Hyeon, Younghee Kim, Sungsu Lim, Min Young Lee, Jieun Kim, Ashwini M Londhe, Lizaveta Gotina, Yunha Kim, Ae Nim Pae, Yong Seo Cho, Jihye Seong, Hyemyung Seo, Yun Kyung Kim, Hyunah Choo, Hoon Ryu, Sun-Joon Min
The present study describes evaluation of epigenetic regulation by a small molecule as the therapeutic potential for treatment of Huntington's disease (HD). We identified 5-allyloxy-2-(pyrrolidin-1-yl)quinoline (APQ) as a novel SETDB1/ESET inhibitor using a combined in silico and in vitro cell based screening system. APQ reduced SETDB1 activity and H3K9me3 levels in a HD cell line model. In particular, not only APQ reduced H3K9me3 levels in the striatum but it also improved motor function and neuropathological symptoms such as neuronal size and activity in HD transgenic (YAC128) mice with minimal toxicity...
December 2021: Journal of Enzyme Inhibition and Medicinal Chemistry
https://read.qxmd.com/read/33642998/d1r-and-d2r-medium-sized-spiny-neurons-diversity-insights-into-striatal-vulnerability-to-huntington-s-disease-mutation
#25
REVIEW
Guendalina Bergonzoni, Jessica Döring, Marta Biagioli
Huntington's disease (HD) is a devastating neurodegenerative disorder caused by an aberrant expansion of the CAG tract within the exon 1 of the HD gene, HTT . HD progressively impairs motor and cognitive capabilities, leading to a total loss of autonomy and ultimate death. Currently, no cure or effective treatment is available to halt the disease. Although the HTT gene is ubiquitously expressed, the striatum appears to be the most susceptible district to the HD mutation with Medium-sized Spiny Neurons (MSNs) (D1R and D2R) representing 95% of the striatal neuronal population...
2021: Frontiers in Cellular Neuroscience
https://read.qxmd.com/read/33369245/neuron-type-specific-increase-in-lamin-b1-contributes-to-nuclear-dysfunction-in-huntington-s-disease
#26
JOURNAL ARTICLE
Rafael Alcalá-Vida, Marta Garcia-Forn, Carla Castany-Pladevall, Jordi Creus-Muncunill, Yoko Ito, Enrique Blanco, Arantxa Golbano, Kilian Crespí-Vázquez, Aled Parry, Guy Slater, Shamith Samarajiwa, Sandra Peiró, Luciano Di Croce, Masashi Narita, Esther Pérez-Navarro
Lamins are crucial proteins for nuclear functionality. Here, we provide new evidence showing that increased lamin B1 levels contribute to the pathophysiology of Huntington's disease (HD), a CAG repeat-associated neurodegenerative disorder. Through fluorescence-activated nuclear suspension imaging, we show that nucleus from striatal medium-sized spiny and CA1 hippocampal neurons display increased lamin B1 levels, in correlation with altered nuclear morphology and nucleocytoplasmic transport disruption. Moreover, ChIP-sequencing analysis shows an alteration of lamin-associated chromatin domains in hippocampal nuclei, accompanied by changes in chromatin accessibility and transcriptional dysregulation...
December 28, 2020: EMBO Molecular Medicine
https://read.qxmd.com/read/33141999/the-c-terminal-fragment-of-the-heavy-chain-of-the-tetanus-toxin-hc-tetx-improves-motor-activity-and-neuronal-morphology-in-the-limbic-system-of-aged-mice
#27
JOURNAL ARTICLE
Ruben Vazquez-Roque, Mariana Pacheco-Flores, Julio Cesar Penagos-Corzo, Gonzalo Flores, José Aguilera, Samuel Treviño, Jorge Guevara, Alfonso Diaz, Berenice Venegas
In the aging process, the brain presents biochemical and morphological alterations. The neurons of the limbic system show reduced size dendrites, in addition to the loss of dendritic spines. These disturbances trigger a decrease in motor and cognitive function. Likewise, it is reported that during aging, in the brain, there is a significant decrease in neurotrophic factors, which are essential in promoting the survival and plasticity of neurons. The carboxyl-terminal fragment of the heavy chain of the tetanus toxin (Hc-TeTx) acts similarly to neurotrophic factors, inducing neuroprotection in different models of neuronal damage...
June 2021: Synapse
https://read.qxmd.com/read/32950559/prenatal-alcohol-exposure-reduces-posterior-dorsomedial-striatum-excitability-and-motivation-in-a-sex-and-age-dependent-fashion
#28
JOURNAL ARTICLE
Victoria Roselli, Changyong Guo, Donald Huang, Di Wen, Daniel Zona, Tiebing Liang, Yao-Ying Ma
Prenatal alcohol exposure (PAE)-induced clinical symptoms have been widely reported but effective treatments are not yet available due to our limited knowledge of the neuronal mechanisms underlying behavioral outputs. Operant behaviors, including both goal-directed and habitual actions, are essential for everyday life. The dorsomedial striatum (DMS) and the dorsolateral striatum (DLS) have been identified as mediating each type of instrumental behavior, respectively. The current studies were designed to evaluate the effects of PAE (i...
September 17, 2020: Neuropharmacology
https://read.qxmd.com/read/32900259/neurobiological-mechanisms-associated-with-antipsychotic-drug-induced-dystonia
#29
REVIEW
Anton Jm Loonen, Svetlana A Ivanova
Dystonia is by far the most intrusive and invalidating extrapyramidal side effect of potent classical antipsychotic drugs. Antipsychotic drug-induced dystonia is classified in both acute and tardive forms. The incidence of drug-induced dystonia is associated with the affinity to inhibitory dopamine D2 receptors. Particularly acute dystonia can be treated with anticholinergic drugs, but the tardive form may also respond to such antimuscarinic treatment, which contrasts their effects in tardive dyskinesia. Combining knowledge of the pathophysiology of primary focal dystonia with the anatomical and pharmacological organization of the extrapyramidal system may shed some light on the mechanism of antipsychotic drug-induced dystonia...
January 2021: Journal of Psychopharmacology
https://read.qxmd.com/read/32877648/overlapping-projections-of-neighboring-direct-and-indirect-pathway-neostriatal-neurons-to-globus-pallidus-external-segment
#30
JOURNAL ARTICLE
Shinichiro Okamoto, Jaerin Sohn, Takuma Tanaka, Megumu Takahashi, Yoko Ishida, Kenta Yamauchi, Masato Koike, Fumino Fujiyama, Hiroyuki Hioki
Indirect pathway medium-sized spiny neurons (iMSNs) in the neostriatum are well known to project to the external segment of the globus pallidus (GPe). Although direct MSNs (dMSNs) also send axon collaterals to the GPe, it remains unclear how dMSNs and iMSNs converge within the GPe. Here, we selectively labeled neighboring dMSNs and iMSNs with green and red fluorescent proteins using an adeno-associated virus vector and examined axonal projections of dMSNs and iMSNs to the GPe in mice. Both dMSNs and iMSNs formed two axonal arborizations displaying topographical projections in the dorsoventral and mediolateral planes...
August 6, 2020: IScience
https://read.qxmd.com/read/32856336/mechanisms-underlying-the-enhancement-of-%C3%AE-aminobutyric-acid-responses-in-the-external-globus-pallidus-of-r6-2-huntington-s-disease-model-mice
#31
JOURNAL ARTICLE
Joshua Barry, Theodore A Sarafian, Joseph B Watson, Carlos Cepeda, Michael S Levine
In Huntington's disease (HD), the output of striatal indirect pathway medium-sized spiny neurons (MSNs) is altered in its target region, the external globus pallidus (GPe). In a previous study we demonstrated that selective optogenetic stimulation of indirect pathway MSNs induced prolonged decay time of γ-aminobutyric acid (GABA) responses in GPe neurons. Here we identified the mechanism underlying this alteration. Electrophysiological recordings in slices from symptomatic R6/2 and wildtype (WT) mice were used to evaluate, primarily, the effects of GABA transporter (GAT) antagonists on responses evoked by optogenetic activation of indirect pathway MSNs...
August 27, 2020: Journal of Neuroscience Research
https://read.qxmd.com/read/32817461/functional-impact-of-the-g279s-substitution-in-the-adenosine-a-1-receptor-a-1-r-g279s-7-44-a-mutation-associated-with-parkinson-s-disease
#32
JOURNAL ARTICLE
Shahrooz Nasrollahi-Shirazi, Daniel Szöllösi, Qiong Yang, Edin Muratspahic, Ali El-Kasaby, Sonja Sucic, Thomas Stockner, Christian Nanoff, Michael Freissmuth
In medium-size, spiny striatal neurons of the direct pathway, dopamine D1 - and adenosine A1 -receptors are coexpressed and are mutually antagonistic. Recently, a mutation in the gene encoding the A1 -receptor (A1 R), A1 R-G279S7.44 , was identified in an Iranian family: two affected offspring suffered from early-onset l-DOPA-responsive Parkinson's disease. The link between the mutation and the phenotype is unclear. Here, we explored the functional consequence of the G279S substitution on the activity of the A1 -receptor after heterologous expression in HEK293 cells...
September 2020: Molecular Pharmacology
https://read.qxmd.com/read/32641371/functional-impact-of-the-g279s-substitution-in-the-adenosine-a1-receptor-a1r-g279s-a-mutation-associated-with-parkinson-s-disease
#33
JOURNAL ARTICLE
Shahrooz Nasrollahi-Shirazi, Daniel Szöllösi, Qiong Yang, Edin Muratspahic, Ali El-Kasaby, Sonja Sucic, Thomas Stockner, Christian Nanoff, Michael Freissmuth
In medium-size, spiny striatal neurons of the direct pathway, dopamine D1 - and adenosine A1 -receptors are co-expressed and are mutually antagonistic. Recently, a mutation in the gene encoding the A1 -receptor (A1 R-G279S7.44 ) was identified in an Iranian family: two affected off-springs suffered from early onset L-DOPA-responsive Parkinson's disease. The link between the mutation and the phenotype is unclear. Here, we explored the functional consequence of the G279S substitution on the activity of the A1 -receptor after heterologous expression in HEK293 cells...
July 8, 2020: Molecular Pharmacology
https://read.qxmd.com/read/32581668/phosphodiesterase-9a-inhibition-facilitates-corticostriatal-transmission-in-wild-type-and-transgenic-rats-that-model-huntington-s-disease
#34
JOURNAL ARTICLE
Shreaya Chakroborty, Fredric P Manfredsson, Alexander M Dec, Peter W Campbell, Grace E Stutzmann, Vahri Beaumont, Anthony R West
Huntington's disease (HD) results from abnormal expansion in CAG trinucleotide repeats within the HD gene, a mutation which leads to degeneration of striatal medium-sized spiny neurons (MSNs), deficits in corticostriatal transmission, and loss of motor control. Recent studies also indicate that metabolism of cyclic nucleotides by phosphodiesterases (PDEs) is dysregulated in striatal networks in a manner linked to deficits in corticostriatal transmission. The current study assessed cortically-evoked firing in electrophysiologically-identified MSNs and fast-spiking interneurons (FSIs) in aged (9-11 months old) wild-type (WT) and BACHD transgenic rats (TG5) treated with vehicle or the selective PDE9A inhibitor PF-04447943...
2020: Frontiers in Neuroscience
https://read.qxmd.com/read/32477064/lack-of-helios-during-neural-development-induces-adult-schizophrenia-like-behaviors-associated-with-aberrant-levels-of-the-trif-recruiter-protein-wdfy1
#35
JOURNAL ARTICLE
Anna Sancho-Balsells, Veronica Brito, Belissa Fernández, Mónica Pardo, Marco Straccia, Silvia Ginés, Jordi Alberch, Isabel Hernández, Belén Arranz, Josep M Canals, Albert Giralt
The role of the WDFY1 protein has been studied as a TLR3/4 scaffold/recruiting protein in the immune system and in different oncogenic conditions. However, its function in brain remains poorly understood. We have found that in mice devoid of Helios (He-/- mice), a transcription factor specifically expressed during the development of the immune cells and the central nervous system, there is a permanent and sustained increase of Wdfy1 gene expression in the striatum and hippocampus. Interestingly, we observed that WDFY1 protein levels were also increased in the hippocampus and dorsolateral prefrontal cortex of schizophrenic patients, but not in the hippocampus of Alzheimer's disease patients with an associated psychotic disorder...
2020: Frontiers in Cellular Neuroscience
https://read.qxmd.com/read/32408403/intracerebral-transplantation-of-bdnf-overexpressing-human-neural-stem-cells-hb1-f3-bdnf-promotes-migration-differentiation-and-functional-recovery-in-a-rodent-model-of-huntington-s-disease
#36
JOURNAL ARTICLE
Hyun Sook Kim, Iksoo Jeon, Jeong-Eun Noh, Hyunseung Lee, Kwan Soo Hong, Nayeon Lee, Zhong Pei, Jihwan Song
Huntington's disease (HD) is a dominantly inherited neurodegenerative disorder caused by abnormally expanded CAG repeats in the huntingtin gene. The huntingtin gene mutation leads to the progressive degeneration of striatal GABAergic medium spiny neurons (MSN) and reduces the level of brain-derived neurotrophic factor (BDNF) in HD patient's brain. BDNF is an essential neurotrophic factor for the cortico-striatal synaptic activity and the survival of GABAergic neurons. In this study, we transplanted BDNF-overexpressing human neural stem cells (HB1...
April 30, 2020: Experimental Neurobiology
https://read.qxmd.com/read/32356172/human-pluripotent-stem-cell-derived-neurons-are-functionally-mature-in-vitro-and-integrate-into-the-mouse-striatum-following-transplantation
#37
JOURNAL ARTICLE
Andrea Comella-Bolla, Javier G Orlandi, Andrés Miguez, Marco Straccia, María García-Bravo, Georgina Bombau, Mireia Galofré, Phil Sanders, Jordi Carrere, José Carlos Segovia, Joan Blasi, Nicholas D Allen, Jordi Alberch, Jordi Soriano, Josep M Canals
Human pluripotent stem cells (hPSCs) are a powerful tool for modelling human development. In recent years, hPSCs have become central in cell-based therapies for neurodegenerative diseases given their potential to replace affected neurons. However, directing hPSCs into specific neuronal types is complex and requires an accurate protocol that mimics endogenous neuronal development. Here we describe step-by-step a fast feeder-free neuronal differentiation protocol to direct hPSCs to mature forebrain neurons in 37 days in vitro (DIV)...
April 30, 2020: Molecular Neurobiology
https://read.qxmd.com/read/32231522/anatomy-and-connectivity-of-the-torus-longitudinalis-of-the-adult-zebrafish
#38
JOURNAL ARTICLE
Mónica Folgueira, Selva Riva-Mendoza, Noelia Ferreño-Galmán, Antonio Castro, Isaac H Bianco, Ramón Anadón, Julián Yáñez
This study describes the cytoarchitecture of the torus longitudinalis (TL) in adult zebrafish by using light and electron microscopy, as well as its main connections as revealed by DiI tract tracing. In addition, by using high resolution confocal imaging followed by digital tracing, we describe the morphology of tectal pyramidal cells (type I cells) that are GFP positive in the transgenic line Tg(1.4dlx5a-dlx6a:GFP) ot1 . The TL consists of numerous small and medium-sized neurons located in a longitudinal eminence attached to the medial optic tectum...
2020: Frontiers in Neural Circuits
https://read.qxmd.com/read/32179863/dynamic-foxp2-levels-in-male-zebra-finches-are-linked-to-morphology-of-adult-born-area-x-medium-spiny-neurons
#39
JOURNAL ARTICLE
Jennifer Kosubek-Langer, Constance Scharff
The transcription factor FOXP2 is crucial for the formation and function of cortico-striatal circuits. FOXP2 mutations are associated with specific speech and language impairments. In songbirds, experimentally altered FoxP2 expression levels in the striatal song nucleus Area X impair vocal learning and song production. Overall FoxP2 protein levels in Area X are low in adult zebra finches and decrease further with singing. However, some Area X medium spiny neurons (MSNs) express FoxP2 at high levels (FoxP2high MSNs) and singing does not change this...
March 16, 2020: Scientific Reports
https://read.qxmd.com/read/32113966/xlr4-as-a-new-candidate-gene-underlying-vulnerability-to-cocaine-effects
#40
JOURNAL ARTICLE
Matteo Di Segni, Sebastian Luca D'Addario, Lucy Babicola, Donald Ielpo, Luisa Lo Iacono, Diego Andolina, Alessandra Accoto, Alessandra Luchetti, Camilla Mancini, Chiara Parisi, Mara D'Onofrio, Ivan Arisi, Rossella Brandi, Tiziana Pascucci, Carlo Cifani, Francesca R D'Amato, Rossella Ventura
Although several studies have been performed in rodents, non-human primates and humans, the biological basis of vulnerability to develop cocaine addiction remains largely unknown. Exposure to critical early events (as Repeated Cross Fostering (RCF)) has been reported to increase sensitivity to cocaine effects in adult C57BL/6J female mice. Using a microarray approach, here we report data showing a strong engagement of X-linked lymphocyte-regulated 4a and 4b (Xlr4) genes in cocaine effects. The expression of Xlr4, a gene involved in chromatin remodeling and dendritic spine morphology, was reduced into the Nucleus Accumbens (NAc) of adult RCF C57BL/6J female...
February 27, 2020: Neuropharmacology
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