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  1. Artikel ; Online: Comparative Hippocampal Proteome and Phosphoproteome in a Niemann-Pick, Type C1 Mouse Model Reveal Insights into Disease Mechanisms.

    Nguyen, Thu T A / Mohanty, Varshasnata / Yan, Ying / Francis, Kevin R / Cologna, Stephanie M

    Journal of proteome research

    2023  Band 23, Heft 1, Seite(n) 84–94

    Abstract: Niemann-Pick disease, type C (NPC) is a neurodegenerative, lysosomal storage disorder in individuals carrying two mutated copies of either ... ...

    Abstract Niemann-Pick disease, type C (NPC) is a neurodegenerative, lysosomal storage disorder in individuals carrying two mutated copies of either the
    Mesh-Begriff(e) Animals ; Mice ; Proteome/genetics ; Proteome/metabolism ; Disease Models, Animal ; Intracellular Signaling Peptides and Proteins/metabolism ; Niemann-Pick Disease, Type C/genetics ; Hippocampus/metabolism
    Chemische Substanzen Proteome ; Intracellular Signaling Peptides and Proteins
    Sprache Englisch
    Erscheinungsdatum 2023-11-24
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, U.S. Gov't, Non-P.H.S. ; Research Support, N.I.H., Extramural
    ZDB-ID 2078618-9
    ISSN 1535-3907 ; 1535-3893
    ISSN (online) 1535-3907
    ISSN 1535-3893
    DOI 10.1021/acs.jproteome.3c00375
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: Factors affecting loneliness among left-behind children.

    Nguyen, Luot V / Nguyen, Thu T A / Trinh, Linh T / Nguyen, Hanh H V

    Current issues in personality psychology

    2023  Band 12, Heft 1, Seite(n) 41–50

    Abstract: Background: In Vietnam, research on the impact of parental migration on left-behind children (LBC) has discussed various dimensions of the subject such as subjective well-being, emotional states, social skills, self-esteem and nutrition of LBC. However, ...

    Abstract Background: In Vietnam, research on the impact of parental migration on left-behind children (LBC) has discussed various dimensions of the subject such as subjective well-being, emotional states, social skills, self-esteem and nutrition of LBC. However, there are still gaps in studies on loneliness among LBC in Vietnam. The study aims to explore the status of loneliness in LBC, including associated protective and risk factors, to make suggestions on preventive measures against LBC's loneliness.
    Participants and procedure: The conveniently selected sample includes 439 LBC in 4 Vietnamese provinces: Thai Nguyen, Bac Ninh, Thai Binh and Nghe An. The mean age is 12.73 (
    Results: The total loneliness score of LBC is 28.62 (
    Conclusions: Perceived social support from friends, care-giving attachment and resilience factors of RAC, RFS, and RHS are protective factors for LBC against loneliness. Parents, teachers and guardians are encouraged to have a close connection with LBC, provide adequate care giving; and create a supportive environment for LBC in pursuing healthy peer relationships and train/improve children's skills to strengthen their resilience.
    Sprache Englisch
    Erscheinungsdatum 2023-04-17
    Erscheinungsland Poland
    Dokumenttyp Journal Article
    ZDB-ID 3030312-6
    ISSN 2353-561X ; 2353-4192
    ISSN (online) 2353-561X
    ISSN 2353-4192
    DOI 10.5114/cipp/162007
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel: Mass spectrometry-based lipid analysis and imaging.

    Pathmasiri, Koralege C / Nguyen, Thu T A / Khamidova, Nigina / Cologna, Stephanie M

    Current topics in membranes

    2021  Band 88, Seite(n) 315–357

    Abstract: Mass spectrometry imaging (MSI) is a powerful tool for in situ mapping of analytes across a sample. With growing interest in lipid biochemistry, the ability to perform such mapping without antibodies has opened many opportunities for MSI and lipid ... ...

    Abstract Mass spectrometry imaging (MSI) is a powerful tool for in situ mapping of analytes across a sample. With growing interest in lipid biochemistry, the ability to perform such mapping without antibodies has opened many opportunities for MSI and lipid analysis. Herein, we discuss the basics of MSI with particular emphasis on MALDI mass spectrometry and lipid analysis. A discussion of critical advancements as well as protocol details are provided to the reader. In addition, strategies for improving the detection of lipids, as well as applications in biomedical research, are presented.
    Mesh-Begriff(e) Lipids ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
    Chemische Substanzen Lipids
    Sprache Englisch
    Erscheinungsdatum 2021-11-09
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ISSN 1063-5823
    ISSN 1063-5823
    DOI 10.1016/bs.ctm.2021.10.005
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel ; Online: Endogenous Protein-Protein Interaction Network of the NPC Cholesterol Transporter 1 in the Cerebral Cortex.

    Javanshad, Roshan / Nguyen, Thu T A / Azaria, Ruth D / Li, Wenping / Edmison, Daisy / Gong, Liang-Wei / Gowrishankar, Swetha / Lieberman, Andrew P / Schultz, Mark L / Cologna, Stephanie M

    Journal of proteome research

    2024  

    Abstract: NPC intracellular cholesterol transporter 1 (NPC1) is a multipass, transmembrane glycoprotein mostly recognized for its key role in facilitating cholesterol efflux. Mutations in ... ...

    Abstract NPC intracellular cholesterol transporter 1 (NPC1) is a multipass, transmembrane glycoprotein mostly recognized for its key role in facilitating cholesterol efflux. Mutations in the
    Sprache Englisch
    Erscheinungsdatum 2024-04-30
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 2078618-9
    ISSN 1535-3907 ; 1535-3893
    ISSN (online) 1535-3907
    ISSN 1535-3893
    DOI 10.1021/acs.jproteome.3c00788
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  5. Artikel: Akap5 links synaptic dysfunction to neuroinflammatory signaling in a mouse model of infantile neuronal ceroid lipofuscinosis.

    Koster, Kevin P / Fyke, Zach / Nguyen, Thu T A / Niqula, Amanda / Noriega-González, Lorena Y / Woolfrey, Kevin M / Dell'Acqua, Mark L / Cologna, Stephanie M / Yoshii, Akira

    Frontiers in synaptic neuroscience

    2024  Band 16, Seite(n) 1384625

    Abstract: Palmitoylation and depalmitoylation represent dichotomic processes by which a labile posttranslational lipid modification regulates protein trafficking and degradation. The depalmitoylating enzyme, palmitoyl-protein thioesterase 1 (PPT1), is associated ... ...

    Abstract Palmitoylation and depalmitoylation represent dichotomic processes by which a labile posttranslational lipid modification regulates protein trafficking and degradation. The depalmitoylating enzyme, palmitoyl-protein thioesterase 1 (PPT1), is associated with the devastating pediatric neurodegenerative condition, infantile neuronal ceroid lipofuscinosis (CLN1). CLN1 is characterized by the accumulation of autofluorescent lysosomal storage material (AFSM) in neurons and robust neuroinflammation. Converging lines of evidence suggest that in addition to cellular waste accumulation, the symptomology of CLN1 corresponds with disruption of synaptic processes. Indeed, loss of Ppt1 function in cortical neurons dysregulates the synaptic incorporation of the GluA1 AMPA receptor (AMPAR) subunit during a type of synaptic plasticity called synaptic scaling. However, the mechanisms causing this aberration are unknown. Here, we used the
    Sprache Englisch
    Erscheinungsdatum 2024-05-10
    Erscheinungsland Switzerland
    Dokumenttyp Journal Article
    ZDB-ID 2592086-8
    ISSN 1663-3563
    ISSN 1663-3563
    DOI 10.3389/fnsyn.2024.1384625
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  6. Artikel ; Online: Discovery of a Small-Molecule Modulator of the Autophagy-Lysosome Pathway That Targets Lamin A/C and LAMP1, Induces Autophagic Flux, and Affects Lysosome Positioning in Neurons.

    Hippman, Ryan S / Snead, Amanda M / Petros, Zoe A / Korkmaz-Vaisys, Melissa A / Patel, Sruchi / Sotelo, Daniel / Dobria, Andrew / Salkovski, Maryna / Nguyen, Thu T A / Linares, Ricardo / Cologna, Stephanie M / Gowrishankar, Swetha / Aldrich, Leslie N

    ACS chemical neuroscience

    2023  Band 14, Heft 24, Seite(n) 4363–4382

    Abstract: Autophagy is a major catabolic degradation and recycling process that maintains homeostasis in cells and is especially important in postmitotic neurons. We implemented a high-content phenotypic assay to discover small molecules that promote autophagic ... ...

    Abstract Autophagy is a major catabolic degradation and recycling process that maintains homeostasis in cells and is especially important in postmitotic neurons. We implemented a high-content phenotypic assay to discover small molecules that promote autophagic flux and completed target identification and validation studies to identify protein targets that modulate the autophagy pathway and promote neuronal health and survival. Efficient syntheses of the prioritized compounds were developed to readily access analogues of the initial hits, enabling initial structure-activity relationship studies to improve potency and preparation of a biotin-tagged pulldown probe that retains activity. This probe facilitated target identification and validation studies through pulldown and competition experiments using both an unbiased proteomics approach and western blotting to reveal Lamin A/C and LAMP1 as the protein targets of compound
    Mesh-Begriff(e) Humans ; Lamin Type A/metabolism ; Autophagy/physiology ; Neurons/metabolism ; Lysosomes/metabolism ; Alzheimer Disease/metabolism ; Lysosomal-Associated Membrane Protein 1/metabolism
    Chemische Substanzen Lamin Type A ; LAMP1 protein, human ; Lysosomal-Associated Membrane Protein 1
    Sprache Englisch
    Erscheinungsdatum 2023-12-09
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ISSN 1948-7193
    ISSN (online) 1948-7193
    DOI 10.1021/acschemneuro.3c00573
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  7. Artikel ; Online: PPARα and PPARγ Signaling Is Enhanced in the Brain of the Naked Mole-Rat, a Mammal that Shows Intrinsic Neuroprotection from Oxygen Deprivation.

    Pergande, Melissa R / Amoroso, Vince G / Nguyen, Thu T A / Li, Wenping / Vice, Emily / Park, Thomas J / Cologna, Stephanie M

    Journal of proteome research

    2021  Band 20, Heft 9, Seite(n) 4258–4271

    Abstract: Naked mole-rats (NMRs) are a long-lived animal that do not develop age-related diseases including neurodegeneration and cancer. Additionally, NMRs have a profound ability to consume reactive oxygen species (ROS) and survive long periods of oxygen ... ...

    Abstract Naked mole-rats (NMRs) are a long-lived animal that do not develop age-related diseases including neurodegeneration and cancer. Additionally, NMRs have a profound ability to consume reactive oxygen species (ROS) and survive long periods of oxygen deprivation. Here, we evaluated the unique proteome across selected brain regions of NMRs at different ages. Compared to mice, we observed numerous differentially expressed proteins related to altered mitochondrial function in all brain regions, suggesting that the mitochondria in NMRs may have adapted to compensate for energy demands associated with living in a harsh, underground environment. Keeping in mind that ROS can induce polyunsaturated fatty acid peroxidation under periods of neuronal stress, we investigated docosahexaenoic acid (DHA) and arachidonic acid (AA) peroxidation under oxygen-deprived conditions and observed that NMRs undergo DHA and AA peroxidation to a far less extent compared to mice. Further, our proteomic analysis also suggested enhanced peroxisome proliferator-activated receptor (PPAR)-retinoid X receptor (RXR) activation in NMRs via the PPARα-RXR and PPARγ-RXR complexes. Correspondingly, we present several lines of evidence supporting PPAR activation, including increased eicosapetenoic and omega-3 docosapentaenoic acid, as well as an upregulation of fatty acid-binding protein 3 and 4, known transporters of omega-3 fatty acids and PPAR activators. These results suggest enhanced PPARα and PPARγ signaling as a potential, innate neuroprotective mechanism in NMRs.
    Mesh-Begriff(e) Animals ; Brain ; Mice ; Mole Rats ; Neuroprotection ; Oxygen ; PPAR alpha/genetics ; PPAR gamma/genetics ; Proteomics
    Chemische Substanzen PPAR alpha ; PPAR gamma ; Oxygen (S88TT14065)
    Sprache Englisch
    Erscheinungsdatum 2021-08-05
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2078618-9
    ISSN 1535-3907 ; 1535-3893
    ISSN (online) 1535-3907
    ISSN 1535-3893
    DOI 10.1021/acs.jproteome.1c00131
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  8. Artikel ; Online: Characterization of the Cerebrospinal Fluid Proteome in Patients with Fragile X-Associated Tremor/Ataxia Syndrome.

    Abbasi, Diana A / Nguyen, Thu T A / Hall, Deborah A / Robertson-Dick, Erin / Berry-Kravis, Elizabeth / Cologna, Stephanie M

    Cerebellum (London, England)

    2021  Band 21, Heft 1, Seite(n) 86–98

    Abstract: Fragile X-associated tremor/ataxia syndrome (FXTAS), first described in 2001, is a neurodegenerative and movement disorder, caused by a premutation in the fragile X mental retardation 1 (FMR1) gene. To date, the biological mechanisms causing this ... ...

    Abstract Fragile X-associated tremor/ataxia syndrome (FXTAS), first described in 2001, is a neurodegenerative and movement disorder, caused by a premutation in the fragile X mental retardation 1 (FMR1) gene. To date, the biological mechanisms causing this condition are still not well understood, as not all premutation carriers develop FXTAS. To further understand this syndrome, we quantitatively compared the cerebrospinal fluid (CSF) proteome of FXTAS patients with age-matched controls using mass spectrometry. We identified 415 proteins of which 97 were altered in FXTAS patients. These proteins suggest changes in acute phase response signaling, liver X receptor/ retinoid X receptor (LXR/RXR) activation, and farnesoid X receptor (FXR)/RXR activation, which are the main pathways found to be affected. Additionally, we detected changes in many other proteins including amyloid-like protein 2, contactin-1, afamin, cell adhesion molecule 4, NPC intracellular cholesterol transporter 2, and cathepsin B, that had been previously noted to hold important roles in other movement disorders. Specific to RXR pathways, several apolipoproteins (APOA1, APOA2, APOA4, APOC2, and APOD) showed significant changes in the CSF of FXTAS patients. Lastly, CSF parameters were analyzed to investigate abnormalities in blood brain barrier function. Correlations were observed between patient albumin quotient values, a measure of permeability, and CGG repeat length as well as FXTAS rating scale scores.
    Mesh-Begriff(e) Ataxia/genetics ; Fragile X Mental Retardation Protein/genetics ; Fragile X Syndrome ; Humans ; Proteome/genetics ; Proteome/metabolism ; Tremor ; Trinucleotide Repeat Expansion
    Chemische Substanzen FMR1 protein, human ; Proteome ; Fragile X Mental Retardation Protein (139135-51-6)
    Sprache Englisch
    Erscheinungsdatum 2021-05-27
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 2112586-7
    ISSN 1473-4230 ; 1473-4222
    ISSN (online) 1473-4230
    ISSN 1473-4222
    DOI 10.1007/s12311-021-01262-7
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Artikel ; Online: Correction to: Characterization of the Cerebrospinal Fluid Proteome in Patients with Fragile X-Associated Tremor/Ataxia Syndrome.

    Abbasi, Diana A / Nguyen, Thu T A / Hall, Deborah A / Robertson-Dick, Erin / Berry-Kravis, Elizabeth / Cologna, Stephanie M

    Cerebellum (London, England)

    2021  Band 21, Heft 1, Seite(n) 99–100

    Sprache Englisch
    Erscheinungsdatum 2021-09-10
    Erscheinungsland United States
    Dokumenttyp Published Erratum
    ZDB-ID 2112586-7
    ISSN 1473-4230 ; 1473-4222
    ISSN (online) 1473-4230
    ISSN 1473-4222
    DOI 10.1007/s12311-021-01321-z
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  10. Artikel: PPARα and PPARγ Signaling Is Enhanced in the Brain of the Naked Mole-Rat, a Mammal that Shows Intrinsic Neuroprotection from Oxygen Deprivation

    Pergande, Melissa R. / Amoroso, Vince G. / Nguyen, Thu T. A. / Li, Wenping / Vice, Emily / Park, Thomas J. / Cologna, Stephanie M.

    Journal of proteome research. 2021 Aug. 05, v. 20, no. 9

    2021  

    Abstract: Naked mole-rats (NMRs) are a long-lived animal that do not develop age-related diseases including neurodegeneration and cancer. Additionally, NMRs have a profound ability to consume reactive oxygen species (ROS) and survive long periods of oxygen ... ...

    Abstract Naked mole-rats (NMRs) are a long-lived animal that do not develop age-related diseases including neurodegeneration and cancer. Additionally, NMRs have a profound ability to consume reactive oxygen species (ROS) and survive long periods of oxygen deprivation. Here, we evaluated the unique proteome across selected brain regions of NMRs at different ages. Compared to mice, we observed numerous differentially expressed proteins related to altered mitochondrial function in all brain regions, suggesting that the mitochondria in NMRs may have adapted to compensate for energy demands associated with living in a harsh, underground environment. Keeping in mind that ROS can induce polyunsaturated fatty acid peroxidation under periods of neuronal stress, we investigated docosahexaenoic acid (DHA) and arachidonic acid (AA) peroxidation under oxygen-deprived conditions and observed that NMRs undergo DHA and AA peroxidation to a far less extent compared to mice. Further, our proteomic analysis also suggested enhanced peroxisome proliferator-activated receptor (PPAR)-retinoid X receptor (RXR) activation in NMRs via the PPARα-RXR and PPARγ-RXR complexes. Correspondingly, we present several lines of evidence supporting PPAR activation, including increased eicosapetenoic and omega-3 docosapentaenoic acid, as well as an upregulation of fatty acid-binding protein 3 and 4, known transporters of omega-3 fatty acids and PPAR activators. These results suggest enhanced PPARα and PPARγ signaling as a potential, innate neuroprotective mechanism in NMRs.
    Schlagwörter Heterocephalus glaber ; arachidonic acid ; brain ; docosahexaenoic acid ; docosapentaenoic acid ; energy ; fatty acid-binding proteins ; gene expression regulation ; hypoxia ; mitochondria ; mole rats ; neurodegenerative diseases ; neurons ; neuroprotective effect ; peroxidation ; proteome ; proteomics ; reactive oxygen species ; research
    Sprache Englisch
    Erscheinungsverlauf 2021-0805
    Umfang p. 4258-4271.
    Erscheinungsort American Chemical Society
    Dokumenttyp Artikel
    ZDB-ID 2078618-9
    ISSN 1535-3907 ; 1535-3893
    ISSN (online) 1535-3907
    ISSN 1535-3893
    DOI 10.1021/acs.jproteome.1c00131
    Datenquelle NAL Katalog (AGRICOLA)

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