keyword
https://read.qxmd.com/read/37018938/highly-pathogenic-natural-monoclonal-antibody-b4-igm-recognizes-a-post-translational-modification-comprised-of-acetylated-n-terminal-methionine-followed-by-aspartic-or-glutamic-acid
#1
JOURNAL ARTICLE
Liudmila Kulik, Brandon Renner, Jennifer Laskowski, Joshua M Thurman, V Michael Holers
The natural monoclonal antibody B4-IgM recognizes murine annexin 4 (mAn4) and exacerbates ischemia-reperfusion injury in many mouse models. During apoptosis, the intracellular mAn4 protein translocates to the membrane surface, remaining attached to the outer membrane leaflet where it is recognized by the anti-mAn4 B4-IgM antibody. B4-IgM does not recognize human annexin 4 (hAn4). However, the B4-IgM antibody epitope was detected by Western blot of unknown human proteins and by flow cytometry on all studied human cell lines undergoing apoptosis and on a minor subset of healthy cells...
April 3, 2023: Molecular Immunology
https://read.qxmd.com/read/36441660/assessment-of-myelin-oligodendrocyte-glycoprotein-antibodies-and-magnetic-resonance-spectroscopy-in-childhood-onset-systemic-lupus-erythematosus
#2
JOURNAL ARTICLE
Huseyin Kilic, Sezgin Sahin, Mekiya Filiz Toprak, Gokce Hale Hatay, Kubra Yilmaz, Amra Adrovic, Kenan Barut, Esin Ozturk Isik, Erdem Tuzun, Osman Kizilkilic, Sema Saltik, Ozgur Kasapcopur
OBJECTIVES: Systemic lupus erythematosus (SLE) is a chronic inflammatory disease characterised by the presence of various autoantibodies. Mild cognitive impairment developing in patients without significant neuropsychiatric (NP) symptoms was thought to be the result of immune-mediated myelinopathy. We aimed to determine the role of myelin oligodendrocyte glycoprotein antibody (MOG-Ab) in the neurological manifestations of childhood-onset SLE (cSLE) and if there is a correlation between various metabolite peaks in magnetic resonance spectroscopy (MRS) and myelinopathy...
November 24, 2022: Clinical and Experimental Rheumatology
https://read.qxmd.com/read/35655925/cerebellar-abnormalities-on-proton-mr-spectroscopy-and-imaging-in-patients-with-gluten-ataxia-a-pilot-study
#3
JOURNAL ARTICLE
Vishwa Rawat, Ritu Tyagi, Inder Singh, Prasenjit Das, Achal Kumar Srivastava, Govind K Makharia, Uma Sharma
Gluten ataxia is a rare immune-mediated neurological disorder caused by the ingestion of gluten. The diagnosis is not straightforward as antibodies are present in only up to 38% of patients, but often at lower titers. The symptoms of ataxia may be mild at the onset but lead to permanent damage if remain untreated. It is characterized by damage to the cerebellum however, the pathophysiology of the disease is not clearly understood. The present study investigated the neurochemical profile of vermis and right cerebellum and structural changes in various brain regions of patients with gluten ataxia ( n = 6, age range 40-65 years) and compared it with healthy controls ( n = 10, 40-55 years)...
2022: Frontiers in Human Neuroscience
https://read.qxmd.com/read/33532185/vegf-b-antibody-and-interleukin-22-fusion-protein-ameliorates-diabetic-nephropathy-through-inhibiting-lipid-accumulation-and-inflammatory-responses
#4
JOURNAL ARTICLE
Yilan Shen, Wei Chen, Lei Han, Qi Bian, Jiajun Fan, Zhonglian Cao, Xin Jin, Tao Ding, Zongshu Xian, Zhiyong Guo, Wei Zhang, Dianwen Ju, Xiaobin Mei
Diabetic nephropathy (DN) is considered the primary causes of end-stage renal disease (ESRD) and is related to abnormal glycolipid metabolism, hemodynamic abnormalities, oxidative stress and chronic inflammation. Antagonism of vascular endothelial growth factor B (VEGF-B) could efficiently ameliorate DN by reducing renal lipotoxicity. However, this pharmacological strategy is far from satisfactory, as it ignores numerous pathogenic factors, including anomalous reactive oxygen species (ROS) generation and inflammatory responses...
January 2021: Acta Pharmaceutica Sinica. B
https://read.qxmd.com/read/33227796/radiological-and-immunostaining-characteristics-of-h3-3-g34r-mutant-glioma-a-report-of-3-cases-and-review-of-the-literature
#5
Shumpei Onishi, Vishwa Jeet Amatya, Vega Karlowee, Yukio Takeshima, Kazuhiko Sugiyama, Kaoru Kurisu, Fumiyuki Yamasaki
INTRODUCTION: H3.3 G34R/V mutation is predominantly identified in the supratentorial nonmidline tumors. However, this tumor is not yet categorized as an entity in 2016 WHO CNS classification. More information is necessary to further determine the characteristics of this tumor. CASE PRESENTATION: Three cases of adolescent hemispheric glioma were treated in our institution. All tumors showed the characteristics of huge tumor size with mild peritumoral edema on T2WI/FLAIR, hyperintense on DWI, and slight partial enhancement by gadolinium...
November 23, 2020: Pediatric Neurosurgery
https://read.qxmd.com/read/28827815/in-vivo-production-of-non-glycosylated-recombinant-proteins-in-nicotiana-benthamiana-plants-by-co-expression-with-endo-%C3%AE-n-acetylglucosaminidase-h-endo-h-of-streptomyces-plicatus
#6
JOURNAL ARTICLE
Tarlan Mamedov, Kader Cicek, Burcu Gulec, Rifat Ungor, Gulnara Hasanova
A plant transient expression system, with eukaryotic post-translational modification machinery, offers superior efficiency, scalability, safety, and lower cost over other expression systems. However, due to aberrant N-glycosylation, this expression system may not be a suitable expression platform for proteins not carrying N-linked glycans in the native hosts. Therefore, it is crucial to develop a strategy to produce target proteins in a non-glycosylated form while preserving their native sequence, conformation and biological activity...
2017: PloS One
https://read.qxmd.com/read/28224137/hmgb1-anti-hmgb1-antibodies-define-a-molecular-signature-of-early-stages-of-hiv-associated-neurocognitive-isorders-hand
#7
JOURNAL ARTICLE
Marie-Lise Gougeon, Béatrice Poirier-Beaudouin, Jacques Durant, Christine Lebrun-Frenay, Héla Saïdi, Valérie Seffer, Michel Ticchioni, Stephane Chanalet, Helene Carsenti, Alexandra Harvey-Langton, Muriel Laffon, Jacqueline Cottalorda, Christian Pradier, Pierre Dellamonica, Matteo Vassallo
BACKGROUND: HIV-associated neurocognitive disorders (HAND) persist in the post-HAART era, characterized by asymptomatic neurocognitive impairment (ANI) and mild neurocognitive disorders (MND). High mobility group box 1 (HMGB1) is a non-histone chromosomal protein widely expressed in the nucleus of all eukaryotic cells, including brain cells, which acts as a potent proinflammatory cytokine when actively secreted from immune cells. Recent reports suggested that HMGB1 acts on microglial cells to promote neuroinflammation...
February 2017: Heliyon
https://read.qxmd.com/read/27714889/comparison-between-proton-magnetic-resonance-spectroscopy-findings-in-dogs-with-tick-borne-encephalitis-and-clinically-normal-dogs
#8
COMPARATIVE STUDY
Christine Sievert, Henning Richter, Katrin Beckmann, Patrick R Kircher, Ines Carrera
In vivo diagnosis of tick-borne encephalitis is difficult due to high seroprevalence and rapid viral clearance, limiting detection of antibodies in blood and cerebrospinal fluid. Magnetic resonance imaging (MRI) characteristics of tick-borne encephalitis have been reported, however MRI studies can also be negative despite the presence of neurologic signs. Magnetic resonance spectroscopy ((1) H MRS) is an imaging method that provides additional information about the metabolic characteristics of brain tissues...
January 2017: Veterinary Radiology & Ultrasound
https://read.qxmd.com/read/26682951/effect-of-histone-acetylation-on-n-methyl-d-aspartate-2b-receptor-subunits-and-interleukin-1-receptors-in-association-with-nociception-related-somatosensory-cortex-dysfunction-in-a-mouse-model-of-sepsis
#9
JOURNAL ARTICLE
Yukio Imamura, Nao Yoshikawa, Yuki Murkami, Satoko Mitani, Naoya Matsumoto, Hisatake Matsumoto, Tomoki Yamada, Kazuma Yamakawa, Junichiro Nakagawa, Hiroshi Ogura, Takeshi Shimazu, Takashi Jin
Whole-body inflammation (i.e., sepsis) often results in brain-related sensory dysfunction. We previously reported that interleukin (IL)-1 resulted in synaptic dysfunction of septic encephalopathy, but the underlying molecular mechanisms remain unknown, as do effective treatments. Using mice, we examined immunohistochemistry, co-immunoprecipitation, enzyme-linked immunosorbent assay, and behavior analyses, and investigated the role of the N-methyl-D-aspartate 2B subunit (NR2B) of NMDA receptor, IL-1 receptor, and histone acetylation in the pathophysiology underlying sensory dysfunction induced by lipopolysaccharide (LPS)...
June 2016: Shock
https://read.qxmd.com/read/26409478/antibody-mediated-oligodendrocyte-remyelination-promotes-axon-health-in-progressive-demyelinating-disease
#10
REVIEW
Bharath Wootla, Aleksandar Denic, Jens O Watzlawik, Arthur E Warrington, Moses Rodriguez
Demyelination underlies early neurological symptoms in multiple sclerosis (MS); however, axonal damage is considered critical for permanent chronic deficits. The precise mechanisms by which axonal injury occurs in MS are unclear; one hypothesis is the absence or failure of remyelination, suggesting that promoting remyelination may protect axons from death. This report provides direct evidence that promoting oligodendrocyte remyelination protects axons and maintains transport function. Persistent Theiler's virus infection of Swiss Jim Lambert (SJL)/J mice was used as a model of MS to assess the effects of remyelination on axonal injury following demyelination in the spinal cord...
October 2016: Molecular Neurobiology
https://read.qxmd.com/read/25924771/a-single-dose-of-a-neuron-binding-human-monoclonal-antibody-improves-brainstem-naa-concentrations-a-biomarker-for-density-of-spinal-cord-axons-in-a-model-of-progressive-multiple-sclerosis
#11
JOURNAL ARTICLE
Bharath Wootla, Aleksandar Denic, Jens O Watzlawik, Arthur E Warrington, Moses Rodriguez
BACKGROUND: Intracerebral infection of susceptible mouse strains with Theiler's murine encephalomyelitis virus (TMEV) results in chronic demyelinating disease with progressive axonal loss and neurologic dysfunction similar to progressive forms of multiple sclerosis (MS). We previously showed that as the disease progresses, a marked decrease in brainstem N-acetyl aspartate (NAA; metabolite associated with neuronal integrity) concentrations, reflecting axon health, is measured. We also demonstrated stimulation of neurite outgrowth by a neuron-binding natural human antibody, IgM12...
April 29, 2015: Journal of Neuroinflammation
https://read.qxmd.com/read/25471565/early-alzheimer-s-disease-neuropathology-detected-by-proton-mr-spectroscopy
#12
JOURNAL ARTICLE
Melissa E Murray, Scott A Przybelski, Timothy G Lesnick, Amanda M Liesinger, Anthony Spychalla, Bing Zhang, Jeffrey L Gunter, Joseph E Parisi, Bradley F Boeve, David S Knopman, Ronald C Petersen, Clifford R Jack, Dennis W Dickson, Kejal Kantarci
Proton magnetic resonance spectroscopy ((1)H-MRS) is sensitive to early neurodegenerative processes associated with Alzheimer's disease (AD). Although (1)H-MRS metabolite ratios of N-acetyl aspartate (NAA)/creatine (Cr), NAA/myoinositol (mI), and mI/Cr measured in the posterior cingulate gyrus reveal evidence of disease progression in AD, pathologic underpinnings of the (1)H-MRS metabolite changes in AD are unknown. Pathologically diagnosed human cases ranging from no likelihood to high likelihood AD (n = 41, 16 females and 25 males) who underwent antemortem (1)H-MRS of the posterior cingulate gyrus at 3 tesla were included in this study...
December 3, 2014: Journal of Neuroscience
https://read.qxmd.com/read/25253433/electroencephalographic-evaluation-for-early-diagnosis-of-limbic-encephalitis
#13
JOURNAL ARTICLE
Maria Elena Pessa, Francesco Janes, Gian Luigi Gigli
Limbic encephalitis (LE) is an inflammation of structures of limbic system. It may be an autoimmune disease or secondary to a neoplasia. Onset is subacute within a few weeks and clinical presentation is characterized by behavioral changes, psychiatric symptoms, short-term memory loss, and epileptic seizures. Diagnosis is typically set after a magnetic resonance imaging (MRI) scan, revealing hyperintensity in limbic structures on T2, fluid-attenuated inversion recovery (FLAIR), and diffusion-weighted imaging (DWI) sequences or detection of antineuronal antibodies; EEG aspecific alterations on temporal areas usually match with MRI and laboratory findings...
July 2016: Clinical EEG and Neuroscience: Official Journal of the EEG and Clinical Neuroscience Society (ENCS)
https://read.qxmd.com/read/24158109/multivoxel-%C3%A2-h-mr-spectroscopy-is-superior-to-contrast-enhanced-mri-for-response-assessment-after-anti-angiogenic-treatment-of-orthotopic-human-glioma-xenografts-and-provides-handles-for-metabolic-targeting
#14
COMPARATIVE STUDY
Bob Hamans, Anna Catharina Navis, Alan Wright, Pieter Wesseling, Arend Heerschap, William Leenders
BACKGROUND: Anti-angiogenic treatment of glioblastoma characteristically results in therapy resistance and tumor progression via diffuse infiltration. Monitoring tumor progression in these patients is thwarted because therapy results in tumor invisibility in contrast-enhanced (CE) MRI. To address this problem, we examined whether tumor progression could be monitored by metabolic mapping using (1)H MR spectroscopic imaging (MRSI). METHODS: We treated groups of BALB/c nu/nu mice carrying different orthotopic diffuse-infiltrative glioblastoma xenografts with bevacizumab (anti-vascular endothelial growth factor [VEGF] antibody, n = 13), cabozantinib (combined VEGF receptor 2/c-Met tyrosine kinase inhibitor, n = 11), or placebo (n = 15) and compared CE-MRI with MRS-derived metabolic maps before, during, and after treatment...
December 2013: Neuro-oncology
https://read.qxmd.com/read/23791710/biomarkers-in-parkinson-s-disease-recent-update
#15
REVIEW
Sushil Sharma, Carolyn Seungyoun Moon, Azza Khogali, Ali Haidous, Anthony Chabenne, Comfort Ojo, Miriana Jelebinkov, Yousef Kurdi, Manuchair Ebadi
Parkinson's disease (PD) is the second most common neurodegenerative disorder mostly affecting the aging population over sixty. Cardinal symptoms including, tremors, muscle rigidity, drooping posture, drooling, walking difficulty, and autonomic symptoms appear when a significant number of nigrostriatal dopaminergic neurons are already destroyed. Hence we need early, sensitive, specific, and economical peripheral and/or central biomarker(s) for the differential diagnosis, prognosis, and treatment of PD. These can be classified as clinical, biochemical, genetic, proteomic, and neuroimaging biomarkers...
September 2013: Neurochemistry International
https://read.qxmd.com/read/22729482/the-relationship-between-cho-naa-and-glioma-metabolism-implementation-for-margin-delineation-of-cerebral-gliomas
#16
JOURNAL ARTICLE
Jun Guo, Chengjun Yao, Hong Chen, Dongxiao Zhuang, Weijun Tang, Guang Ren, Yin Wang, Jinsong Wu, Fengping Huang, Liangfu Zhou
BACKGROUND: The marginal delineation of gliomas cannot be defined by conventional imaging due to their infiltrative growth pattern. Here we investigate the relationship between changes in glioma metabolism by proton magnetic resonance spectroscopic imaging ((1)H-MRSI) and histopathological findings in order to determine an optimal threshold value of choline/N-acetyl-aspartate (Cho/NAA) that can be used to define the extent of glioma spread. METHOD: Eighteen patients with different grades of glioma were examined using (1)H-MRSI...
August 2012: Acta Neurochirurgica
https://read.qxmd.com/read/22304706/tissue-distribution-of-glutamate-carboxypeptidase-ii-gcpii-with-a-focus-on-the-central-and-peripheral-nervous-system
#17
REVIEW
P Marmiroli, B Slusher, G Cavaletti
Glutamate carboxypeptidase II, also known as prostate specific membrane antigen or folate hydrolase I, is a type II transmembrane 750 amino acid membrane-bound glycoprotein, with a molecular weight in the human form of approximately 100 kDa and a demonstrated metallopeptidase activity. At the synaptic level it hydrolyzes N-acetylaspartylglutamate to N-acetyl-aspartate and glutamate. Its localization in the animal and human nervous system has only recently been clearly established, since many of the older studies gave conflicting results, likely due to the use of poorly characterized antibodies lacking epitope mapping and proper controls (i...
2012: Current Medicinal Chemistry
https://read.qxmd.com/read/21598311/extensive-aspartoacylase-expression-in-the-rat-central-nervous-system
#18
JOURNAL ARTICLE
John R Moffett, Peethambaran Arun, Prasanth S Ariyannur, James Y Garbern, David M Jacobowitz, Aryan M A Namboodiri
Aspartoacylase (ASPA) catalyzes deacetylation of N-acetylaspartate (NAA) to generate acetate and aspartate. Mutations in the gene for ASPA lead to reduced acetate availability in the CNS during development resulting in the fatal leukodystrophy Canavan disease. Highly specific polyclonal antibodies to ASPA were used to examine CNS expression in adult rats. In white matter, ASPA expression was associated with oligodendrocyte cell bodies, nuclei, and some processes, but showed a dissimilar distribution pattern to myelin basic protein and oligodendrocyte specific protein...
October 2011: Glia
https://read.qxmd.com/read/20051687/familial-creutzfeldt-jakob-disease-with-a-v180i-mutation-comparative-analysis-with-pathological-findings-and-diffusion-weighted-images
#19
COMPARATIVE STUDY
Kazuo Mutsukura, Katsuya Satoh, Susumu Shirabe, Itsuro Tomita, Takayasu Fukutome, Minoru Morikawa, Masachika Iseki, Kensuke Sasaki, Yusei Shiaga, Tetsuyuki Kitamoto, Katsumi Eguchi
BACKGROUND: Diffusion-weighted imaging (DWI) has been reported to be a useful technique for diagnosing Creutzfeldt-Jakob disease (CJD). The present study reported DWI results in cases of familial CJD with a V180I mutation (CJD180) in the prion protein gene as well as neurological findings. METHODS: A retrospective analysis of 3 patients with V180I was performed. Cerebrospinal fluid (CSF) analysis, brain MRI, single-photon emission computed tomography (SPECT), and magnetic resonance spectroscopy (MRS) were included...
2009: Dementia and Geriatric Cognitive Disorders
https://read.qxmd.com/read/19811606/amyloid-precursor-protein-695-associates-with-assembled-nr2a-and-nr2b-containing-nmda-receptors-to-result-in-the-enhancement-of-their-cell-surface-delivery
#20
JOURNAL ARTICLE
Sarah L Cousins, Sarah E A Hoey, F Anne Stephenson, Michael S Perkinton
This is a study of the interaction between the two NMDA neurotransmitter receptor subtypes, NR1/NR2A and NR1/NR2B, and amyloid precursor protein (APP) 695, the major APP variant expressed in neurones. APP695 co-immunoprecipitated with assembled NR1-1a/NR2A and NR1-1a/NR2B NMDA receptors following expression in mammalian cells. Single NR1-1a, NR1-2a, NR1-4b(c-Myc), or NR2 subunit transfections revealed that co-association of APP695 with assembled NMDA receptors was mediated via the NR1 subunit; it was independent of the NR1 C1, C2, and C2' cassettes and, the use of an NR1-2a(c-Myc)-trafficking mutant suggested that interaction between the two proteins occurs in the endoplasmic reticulum...
December 2009: Journal of Neurochemistry
keyword
keyword
119662
1
2
Fetch more papers »
Fetching more papers... Fetching...
Remove bar
Read by QxMD icon Read
×

Save your favorite articles in one place with a free QxMD account.

×

Search Tips

Use Boolean operators: AND/OR

diabetic AND foot
diabetes OR diabetic

Exclude a word using the 'minus' sign

Virchow -triad

Use Parentheses

water AND (cup OR glass)

Add an asterisk (*) at end of a word to include word stems

Neuro* will search for Neurology, Neuroscientist, Neurological, and so on

Use quotes to search for an exact phrase

"primary prevention of cancer"
(heart or cardiac or cardio*) AND arrest -"American Heart Association"

We want to hear from doctors like you!

Take a second to answer a survey question.