Topographic distribution of scrapie amyloid-immunoreactive plaques in chronic wasting disease in captive mule deer (Odocoileus hemionus hemionus).

Abstract:

:Chronic wasting disease (CWD), a progressive neurological disorder of captive mule deer, black-tailed deer, hybrids of mule deer and white-tailed deer and Rocky Mountain elk, is characterized neuropathologically by widespread spongiform change of the neuropil, intracytoplasmic vacuolation in neuronal perikarya and astrocytic hypertrophy and hyperplasia. We report the topographic distribution of amyloid plaques reactive to antibodies prepared against scrapie amyloid in CWD-affected captive mule deer (Odocoileus hemionus hemionus). Scrapie amyloid-immunoreactive plaques were found in the cerebral gray and white matter, in deep subcortical nuclei, in isolation or in clusters in areas of vacuolation, and perivascularly, in subpial and subependymal regions. In the cerebellum, immunoreactive amyloid plaques were observed in the molecular, pyramidal and granular layers. Scrapie amyloid-immunoreactive deposits were also seen in neuronal perikarya. Furthermore, amyloid plaques in CWD-affected captive mule deer were alcianophilic at 0.3 M magnesium chloride indicating the presence of weakly to moderately sulfated glycosaminoglycans. Our data corroborate that CWD in captive mule deer belongs to the subacute virus spongiform encephalopathies.

journal_name

Acta Neuropathol

journal_title

Acta neuropathologica

authors

Guiroy DC,Williams ES,Yanagihara R,Gajdusek DC

doi

10.1007/BF00310125

subject

Has Abstract

pub_date

1991-01-01 00:00:00

pages

475-8

issue

5

eissn

0001-6322

issn

1432-0533

journal_volume

81

pub_type

杂志文章
  • Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment.

    abstract::A case of Creutzfeldt-Jakob disease (CJD) with a rare mutation of the prion protein (PrP) gene (PRNP) at codon 208 (R208H) is described. By comparison with two preceding reports, the case described here displayed two distinct biochemical and neuropathological features. Western blot analysis of brain homogenates showed...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-004-0978-0

    authors: Roeber S,Krebs B,Neumann M,Windl O,Zerr I,Grasbon-Frodl EM,Kretzschmar HA

    更新日期:2005-04-01 00:00:00

  • The relationship between Bunina bodies, skein-like inclusions and neuronal loss in amyotrophic lateral sclerosis.

    abstract::Specific pathological hallmarks have been described in amyotrophic lateral sclerosis (ALS), which include motor neuronal loss, Bunina bodies (BBs) and skein like inclusions (SLIs). We investigated the relation between these three lesions in the cervical and lumbar anterior horns and the hypoglossal nuclei of 20 ALS pa...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-001-0507-3

    authors: van Welsem ME,Hogenhuis JA,Meininger V,Metsaars WP,Hauw JJ,Seilhean D

    更新日期:2002-06-01 00:00:00

  • Concomitant Creutzfeldt-Jakob and Alzheimer diseases.

    abstract::We report a 69-year-old female with cerebral and cerebellar symptomatology of 15-month duration. At autopsy, both panencephalopathic Creutzfeldt-Jakob and plaque-predominant Alzheimer diseases were found. Plaque amyloid was exclusively of the beta/A4 type, but abundant abnormal protease-resistant protein was identifie...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00294437

    authors: Powers JM,Liu Y,Hair LS,Kascsack RJ,Lewis LD,Levy LA

    更新日期:1991-01-01 00:00:00

  • Expression of glial fibrillary acidic protein in human glioma cell lines as detected by molecular hybridization.

    abstract::The expression of glial fibrillary acidic protein (GFAP) in continuous glioma and non-glioma cell lines was evaluated by molecular hybridization and immunocytochemistry. RNA transcripts from the GFAP gene were detected in two of six cell lines by Northern blot analysis of cellular RNAs using a cloned mouse GFAP cDNA p...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00688264

    authors: Dewhurst S,Stevenson M,McComb RD,Volsky DJ

    更新日期:1987-01-01 00:00:00

  • Loss of fragile X mental retardation protein precedes Lewy pathology in Parkinson's disease.

    abstract::Parkinson's disease (PD) is the most common neurodegenerative movement disorder and is characterized by the progressive loss of dopaminergic (DA) neurons in the substantia nigra pars compacta (SNc) and the gradual appearance of α-synuclein (α-syn)-containing neuronal protein aggregates. Although the exact mechanism of...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-019-02099-5

    authors: Tan Y,Sgobio C,Arzberger T,Machleid F,Tang Q,Findeis E,Tost J,Chakroun T,Gao P,Höllerhage M,Bötzel K,Herms J,Höglinger G,Koeglsperger T

    更新日期:2020-02-01 00:00:00

  • Ultrastructural study of aggregates in the spinal cord of transgenic mice with a G93A mutant SOD1 gene.

    abstract::The ultrastructural features of SOD1-positive aggregates were determined to clarify whether these aggregates are associated with the pathogenesis of SOD1 mutant mice. We examined the spinal cord of transgenic mice expressing a G93A mutant human SOD1 gene with fewer copies (gene copy 10). At the early presymptomatic st...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-004-0939-7

    authors: Sasaki S,Warita H,Murakami T,Shibata N,Komori T,Abe K,Kobayashi M,Iwata M

    更新日期:2005-03-01 00:00:00

  • mTOR-dependent abnormalities in autophagy characterize human malformations of cortical development: evidence from focal cortical dysplasia and tuberous sclerosis.

    abstract::Focal cortical dysplasia (FCD) is a localized malformation of cortical development and is the commonest cause of severe childhood epilepsy in surgical practice. Children with FCD are severely disabled by their epilepsy, presenting with frequent seizures early in life. The commonest form of FCD in children is character...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-013-1135-4

    authors: Yasin SA,Ali AM,Tata M,Picker SR,Anderson GW,Latimer-Bowman E,Nicholson SL,Harkness W,Cross JH,Paine SM,Jacques TS

    更新日期:2013-08-01 00:00:00

  • Astroblastoma revisited: a report of three cases.

    abstract::The very existence of astroblastoma has been a question of considerable controversy, although there appears now to be sufficient documentation to establish it as a tenable entity. Due to the rarity of this tumor, little information exists in the literature as to its natural history, efficacy of therapy and its patholo...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00689508

    authors: Hoag G,Sima AA,Rozdilsky B

    更新日期:1986-01-01 00:00:00

  • Neuronopathic juvenile glucosylceramidosis due to sap-C deficiency: clinical course, neuropathology and brain lipid composition in this Gaucher disease variant.

    abstract::Glucosylceramide lipidosis results from a defective lysosomal degradation of this glycolipid. Lipid degradation is controlled by two components, the enzyme beta-glucocerebrosidase and a sphingolipid activator protein. While most Gaucher cases are due to mutations within the gene that codes for the lysosomal enzyme, on...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s004010050960

    authors: Pàmpols T,Pineda M,Girós ML,Ferrer I,Cusi V,Chabás A,Sanmarti FX,Vanier MT,Christomanou H

    更新日期:1999-01-01 00:00:00

  • Alpha-chemokine receptors CXCR1-3 and their ligands in idiopathic inflammatory myopathies.

    abstract::The idiopathic inflammatory myopathies (IIM) are a heterogeneous group of neuromuscular disorders subdivided into polymyositis (PM), sporadic inclusion body myositis (sIBM) and dermatomyositis (DM). Chemokines play an essential role in sustained inflammation associated with IIM. We studied the distribution of the alph...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-005-0989-5

    authors: De Paepe B,De Keyzer K,Martin JJ,De Bleecker JL

    更新日期:2005-06-01 00:00:00

  • Differentiation of classic medulloblastoma into metastatic large cell medulloblastoma with focal rhabdoid differentiation in the absence of posterior fossa recurrence.

    abstract::A case of classic medulloblastoma that metastasized, despite the absence of local recurrence, to extraneural sites 7 years after treatment is reported. The metastases were, in contrast to the primary tumor, of large cell type and displayed abortive myogenic and, in one site, also rhabdoid differentiation. The primary ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-005-0986-8

    authors: Donner LR

    更新日期:2005-05-01 00:00:00

  • Nervous system involvement in von Hippel-Lindau disease: pathology and mechanisms.

    abstract::Patients with von Hippel-Lindau disease carry a germline mutation of the Von Hippel-Lindau (VHL) tumor-suppressor gene. We discuss the molecular consequences of loss of VHL gene function and their impact on the nervous system. Dysfunction of the VHL protein causes accumulation and activation of hypoxia inducible facto...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章,评审

    doi:10.1007/s00401-013-1091-z

    authors: Vortmeyer AO,Falke EA,Gläsker S,Li J,Oldfield EH

    更新日期:2013-03-01 00:00:00

  • Expression of smooth muscle proteins in cavernous and arteriovenous malformations.

    abstract::Cavernous malformations (CVMs) and arteriovenous malformations (AVMs) were immunostained for three smooth muscle cell (SMC)-specific protein markers (smooth muscle alpha-actin, SM1 and SM2). Smooth muscle alpha-actin, a widely used marker of SMCs, is reportedly one of the earliest proteins expressed during differentia...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s004010100362

    authors: Hoya K,Asai A,Sasaki T,Kimura K,Kirino T

    更新日期:2001-09-01 00:00:00

  • High binding of CS2 sulphur in spinal cord axonal fraction.

    abstract::The binding of carbon disulphide sulphur was studied in the spinal cord and its axons of four control and four phenobarbitone pretreated adult rats 3 and 6 h after an intraperitoneal injection of 650 mumol of CS2 in olive oil. The binding of CS2 carbon was measured in the same fractions of two adult control rats 4.5 h...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00685369

    authors: Savolainen H,Vainio H

    更新日期:1976-11-15 00:00:00

  • Cytoskeletal properties and endogenous degradation of glial fibrillary acidic protein and vimentin in cultured human glioma cells.

    abstract::The cytoskeletal properties and endogenous degradation of intermediate filaments in cultured human glioma cells (U-251MG) were studied using monoclonal antibodies in immunohistochemical and immunochemical methods. Both glial fibrillary acidic protein (GFAP)- and vimentin-antibodies gave a fibrillar cytoplasmic stainin...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00687041

    authors: Paetau A,Virtanen I

    更新日期:1986-01-01 00:00:00

  • Immunological and pathological findings in demyelinating encephalitis associated with canine distemper virus infection.

    abstract::Nine dogs with canine distemper encephalitis (CDE) were examined with immunological techniques including demonstration of antibodies against canine distemper virus (CDV) in the serum and against myelin basic protein (MBP) in serum and in CSF. Mitogen stimulation tests of lymphocytes were also done. The brains were exa...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00691174

    authors: Vandevelde M,Kristensen F,Kristensen B,Steck AJ,Kihm U

    更新日期:1982-01-01 00:00:00

  • A missense mutation in the WD40 domain of murine Lyst is linked to severe progressive Purkinje cell degeneration.

    abstract::Disturbance of intracellular trafficking plays a major role in several neurodegenerative disorders including Alzheimer or Parkinson's disease. The Chediak-Higashi syndrome (CHS), a life-threatening autosomal recessive disease with frequent mutations in the LYST gene, and its animal model, the beige mouse, are both cha...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-006-0092-6

    authors: Rudelius M,Osanger A,Kohlmann S,Augustin M,Piontek G,Heinzmann U,Jennen G,Russ A,Matiasek K,Stumm G,Schlegel J

    更新日期:2006-09-01 00:00:00

  • Golgi study on brain of macular mutant mouse as a model of Menkes kinky hair disease.

    abstract::This study was undertaken to elucidate, using the Golgi method, the neuropathological change in the brain of the macular mutant mouse, whose hemizygote (Ml/y) is considered to be a model of Menkes kinky hair disease (MKHD). The hemizygote mice gradually lost weight after 10 days of age and died with emaciation and sei...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00687266

    authors: Kawasaki H,Onaga A,Yamano T,Shimada M,Nishimura M

    更新日期:1987-01-01 00:00:00

  • FUS pathology in ALS is linked to alterations in multiple ALS-associated proteins and rescued by drugs stimulating autophagy.

    abstract::Amyotrophic lateral sclerosis (ALS) is a lethal disease characterized by motor neuron degeneration and associated with aggregation of nuclear RNA-binding proteins (RBPs), including FUS. How FUS aggregation and neurodegeneration are prevented in healthy motor neurons remain critically unanswered questions. Here, we use...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-019-01998-x

    authors: Marrone L,Drexler HCA,Wang J,Tripathi P,Distler T,Heisterkamp P,Anderson EN,Kour S,Moraiti A,Maharana S,Bhatnagar R,Belgard TG,Tripathy V,Kalmbach N,Hosseinzadeh Z,Crippa V,Abo-Rady M,Wegner F,Poletti A,Troost D,A

    更新日期:2019-07-01 00:00:00

  • In situ analysis of cell kinetics in human brain tumors. A comparative immunocytochemical study of S phase cells by a new in vitro bromodeoxyuridine-labeling technique, and of proliferating pool cells by monoclonal antibody Ki-67.

    abstract::A newly developed in vitro labeling method with bromodeoxyuridine (BrdU) identifies S phase cells in situ in freshly obtained surgical tissue of human brain tumors which is subsequently fixed and embedded in paraffin for BrdU immunovisualization. For the first time, the BrdU labeling index (LI) is successfully compare...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00687579

    authors: Morimura T,Kitz K,Budka H

    更新日期:1989-01-01 00:00:00

  • Bicuculline-induced epileptic brain injury. Transient and persistent cell changes in rat cerebral cortex in the early recovery period.

    abstract::It was earlier shown that bicuculline-induced status epilepticus gives rise to profound acute changes in the rat cerebral cortex, i.e. edema and neuronal alterations. In the present study, we explored to what extent interruption of the seizure activity reverses the changes observed. To that end, status epilepticus of ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00684924

    authors: Söderfeldt B,Kalimo H,Olsson Y,Siesjö BK

    更新日期:1983-01-01 00:00:00

  • In situ hybridization of myoglobin mRNA: results on the skeletal muscles of normal subjects and patients with neuromuscular diseases.

    abstract::The intracellular localization of myoglobin(Mb) mRNA in the skeletal muscles of normal subjects and patients with Duchenne muscular dystrophy(DMD) or amyotrophic lateral sclerosis(ALS) was examined by in situ hybridization using a biotin-labeled cDNA probe. In cross sections of normal muscles, Mb mRNA signals were dem...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00369442

    authors: Mitsui T,Kawai H,Naruo T,Nishino H,Saito S

    更新日期:1993-01-01 00:00:00

  • Thrombosis of a saccular microaneurysm causing cerebral (pontine) lacunae.

    abstract::The authors present the case of a hypertensive patient with a thrombosis of a saccular microaneurysm (SMA) and underlying cerebral (pontine) lacunae. This SMA lay at the junction between the main vessel and two small feeding arteries penetrating into the necrotic territory. Microhemorrhages were observed in and outsid...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00688313

    authors: Benhaiem-Sigaux N,Gherardi R,Salama J,Gray F,Amouroux J,Poirier J

    更新日期:1986-01-01 00:00:00

  • Protein aggregation in amyotrophic lateral sclerosis.

    abstract::Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by the aggregation of ubiquitinated proteins in affected motor neurons. Recent studies have identified several new molecular constituents of ALS-linked cellular aggregates, including FUS, TDP-43, OPTN, UBQLN2 and the translational product...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章,评审

    doi:10.1007/s00401-013-1125-6

    authors: Blokhuis AM,Groen EJ,Koppers M,van den Berg LH,Pasterkamp RJ

    更新日期:2013-06-01 00:00:00

  • N-Hexane- and methylethylketone-induced polyneuropathy. Abnormal accumulation of glycogen in unmyelinated axons. Report of a case.

    abstract::This report presents the ultrastructural nerve study of a patient with sensorimotor neuropathy by a shoe glue containing an association of n-hexane and methylethylketone. Giant axons, distended by microfilamentous proliferation typical of such cases of neuropathy, were found in significant amounts. An unusual histolog...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00690990

    authors: Vallat JM,Leboutet MJ,Loubet A,Piva C,Dumas M

    更新日期:1981-01-01 00:00:00

  • Tumor necrosis factor-alpha, microglia and astrocytes in AIDS dementia complex.

    abstract::The pathogenesis of HIV-associated cognitive changes is poorly understood. Cytokines such as tumor necrosis factor-alpha (TNF-alpha) have been postulated to contribute to the mechanism of the neurological complications of HIV infection. One of the effects of TNF-alpha is to induce astrocyte proliferation in vitro. The...

    journal_title:Acta neuropathologica

    pub_type: 临床试验,杂志文章

    doi:10.1007/s004010050646

    authors: Seilhean D,Kobayashi K,He Y,Uchihara T,Rosenblum O,Katlama C,Bricaire F,Duyckaerts C,Hauw JJ

    更新日期:1997-05-01 00:00:00

  • Evidence for tangential migration disturbances in human lissencephaly resulting from a defect in LIS1, DCX and ARX genes.

    abstract::During corticogenesis, neurons adopt different migration pathways to reach their final position. The precursors of pyramidal neurons migrate radially, whereas most of the GABA-containing interneurons are generated in the ventral telencephalon and migrate tangentially into the neocortex. Then, they use a radial migrati...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-010-0692-z

    authors: Marcorelles P,Laquerrière A,Adde-Michel C,Marret S,Saugier-Veber P,Beldjord C,Friocourt G

    更新日期:2010-10-01 00:00:00

  • Immunogold localization of the 43-kDa dystroglycan at the plasma membrane in control and dystrophic human muscle.

    abstract::Immunofluorescence and immunogold labelling were used to localise the 43-kDa dystrophin-associated glycoprotein (43DAG) of the dystrophin-glycoprotein complex in control and Duchenne muscular dystrophy (DMD) biopsies. In control muscle 43DAG was localised by immunofluorescence to the periphery of the fibre and, by imm...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00313603

    authors: Cullen MJ,Walsh J,Nicholson LV

    更新日期:1994-01-01 00:00:00

  • Intracytoplasmic eosinophilic inclusions in the neurons of the central nervous system.

    abstract::This study reports the histological, ultrastructural, and immunocytochemical characteristics of intracytoplasmic eosinophilic inclusion bodies occurring in various types of neurons of the human central nervous system. By light microscopy, the inclusions were brightly eosinophilic, slightly birefringent, and sharply de...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00308960

    authors: Peña CE,Katoh A

    更新日期:1989-01-01 00:00:00

  • Intrasellar malignant lymphoma developing within pituitary adenoma.

    abstract::A mixed lymphoblastic T cell lymphoma and gonadotroph cell pituitary adenoma occurred 25 years after first resection of the adenoma. Within 1 year the lymphoma overgrew the adenoma, but was still restricted to the sellar region. Histologically, lymphoma and adenoma components were tightly admixed. Possible pathogeneti...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s004010050990

    authors: Kuhn D,Buchfelder M,Brabletz T,Paulus W

    更新日期:1999-03-01 00:00:00