Postnatal porencephaly induced in mouse by murine cytomegalovirus.

Abstract:

:Mouse embryos were infected with murine cytomegalovirus (MCMV) by injecting the virus into the cerebral ventricles at the late gestation. After deliveries, offspring were fed by the mothers until 4 weeks. Cystic brain lesions, regarded as porencephaly or paraventricular cysts, were observed in about 20% of the MCMV-injected offspring 3 to 4 weeks after birth. The porencephaly involved the cerebral cortex and the white matter, and sometimes opened to the ventricles, while the paraventricular cysts involved the white matter. The inner surfaces of the cysts were covered with thin monolayer cells. Around the cystic lesions, perivascular cuffings were sometimes observed in the meninges and the basal regions. Viral antigen-positive cells were observed in the cortex and the hippocampus but were hardly observed along the cystic walls. Immunohistochemical double staining using antibodies specific for the viral antigen and specific for factor VIII-related antigen showed that the brain capillary endothelial cells had susceptibility to MCMV infection, and in addition that some neurons in the cortex and the hippocampus had the same susceptibility. These findings suggest that there are at least two ways by which MCMV induce abnormalities in the developing mouse brains; migration of MCMV-infected neurons and affinity to the endothelial cells of the brain vessels to this virus.

journal_name

Acta Neuropathol

journal_title

Acta neuropathologica

authors

Tsutsui Y,Kashiwai A,Kawamura N,Kadota C,Nagahama M

doi

10.1007/BF00293377

subject

Has Abstract

pub_date

1991-01-01 00:00:00

pages

435-41

issue

6

eissn

0001-6322

issn

1432-0533

journal_volume

82

pub_type

杂志文章
  • Ultrastructure of cerebellar capillary hemangioblastoma. III. Crystalloid bodies in endothelial cells.

    abstract::The endothelial cells of three cases of cerebellar capillary hemangioblastoma were studied by means of electron microscopy. Crystalloid bodies, not previously described in the vessels of the central nervous system (CNS), were found in 5%-10% of the endothelial cells, more often in the capillaries with small irregular ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00688686

    authors: Ho KL

    更新日期:1985-01-01 00:00:00

  • The neuropathology of cerebrotendinous xanthomatosis revisited: a case report and review of the literature.

    abstract::Cerebrotendinous xanthomatosis (CTX), a rare autosomal-recessive lipid storage disease, has been well characterized clinically and biochemically, and recently also from the molecular biological aspect. However, only a very few publications deal with its neuropathology, and views on its pathogenesis vary. Based on a re...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00294324

    authors: Soffer D,Benharroch D,Berginer V

    更新日期:1995-01-01 00:00:00

  • Niemann-Pick disease type C. Study on the nature of the cerebral storage process.

    abstract::A complex neuropathological study of two cases of Niemann-Pick disease (NPD) type C (NPDC) revealed some novel features in the chemical pathology of the neuronal storage. Lipid histochemistry showed the presence of a lipid which met the criteria of a neuronal glycosphingolipid. Sphingomyelin (SM) was not detected in t...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00690966

    authors: Elleder M,Jirásek A,Smíd F,Ledvinová J,Besley GT

    更新日期:1985-01-01 00:00:00

  • Excitatory amino acid transporter 1 and 2 immunoreactivity in the spinal cord in amyotrophic lateral sclerosis.

    abstract::The spinal cord of 20 patients with amyotrophic lateral sclerosis (ALS) and 5 patients with lower motor neuron disease (LMND) were investigated immunohistochemically using anti-human excitatory amino acid transporter 1 (EAAT1) and EAAT2 antibodies which are the astrocytic transporters. The purpose of the study was to ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s004019900159

    authors: Sasaki S,Komori T,Iwata M

    更新日期:2000-08-01 00:00:00

  • Formation of amyloid-beta oligomers in brain vascular smooth muscle cells transiently exposed to iron-induced oxidative stress.

    abstract::Vascular smooth muscle cells are involved in deposition of amyloid in brain blood vessels. Accumulation of amyloid-beta peptide (Abeta) in cultured brain vascular smooth muscle cells that overexpress human amyloid-beta precursor protein (APP) Swedish, is strongly enhanced by exposure to iron ions. We studied cellular ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-009-0497-0

    authors: Frackowiak J,Potempska A,Mazur-Kolecka B

    更新日期:2009-05-01 00:00:00

  • Expression of serine proteases and metalloproteinases in human pituitary adenomas and anterior pituitary lobe tissue.

    abstract::Data on the dural invasiveness of pituitary adenomas have been correlated to the expression of matrix metalloproteinases (e.g. MMP-9). Serine proteases have not yet been investigated in human pituitary adenomas. In this study, paraffin-embedded material from 84 human pituitary adenomas (acromegaly n=18, Cushing's dise...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-003-0747-5

    authors: Knappe UJ,Hagel C,Lisboa BW,Wilczak W,Lüdecke DK,Saeger W

    更新日期:2003-11-01 00:00:00

  • Progressive supranuclear palsy with palatal myoclonus.

    abstract::We present a case of progressive supranuclear palsy (PSP) with palatal myoclonus occurred in a 64-year-old man. The nucleus olivaris of the medulla oblongata showed high signal intensity on T2-weighted MR images, indicating brainstem tegmental atrophy, which were confirmed as hypertrophy of the nucleus inferior olivar...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s004010050706

    authors: Suyama N,Kobayashi S,Isino H,Iijima M,Imaoka K

    更新日期:1997-09-01 00:00:00

  • Constant and severe involvement of Betz cells in corticobasal degeneration is not consistent with pyramidal signs: a clinicopathological study of ten autopsy cases.

    abstract::This report concerns a clinicopathological study of three additional patients with corticobasal degeneration (CBD), described here for the first time, and a clinicopathological correlation between pyramidal signs and upper motor neuron involvement, in ten autopsy cases of CBD, including seven cases reported by us prev...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章,评审

    doi:10.1007/s00401-004-0966-4

    authors: Tsuchiya K,Murayama S,Mitani K,Oda T,Arima K,Mimura M,Nagura H,Haga C,Akiyama H,Yamanouchi H,Mizusawa H

    更新日期:2005-04-01 00:00:00

  • Histological changes of neuronal damage in vegetative dogs induced by 18 minutes of complete global brain ischemia: two-phase damage of Purkinje cells and hippocampal CA1 pyramidal cells.

    abstract::We have developed a functional vegetative model by an 18-min clamping of the ascending aorta combined with a bypass formation between the aorta to right atrium and the aorta to femoral vein. Complete global brain ischemia (CGBI) induced for 18 min with this model provided the following distinct advantages: cardiopulmo...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00294614

    authors: Sato M,Hashimoto H,Kosaka F

    更新日期:1990-01-01 00:00:00

  • Same axonal regeneration rate after different endoneurial response to intraneural glycerol and phenol injection.

    abstract::Glycerol (an atoxic alcohol) and phenol (a toxic monohydroxybenzene) are currently used as neurolytic blocking agents to relieve pain or spasticity. In the present study we compared the endoneurial response of anhydrous glycerol and 7% phenol-aqua after intraneural injection into rat sciatic nerve, using electron micr...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s004010000349

    authors: Westerlund T,Vuorinen V,Röyttä M

    更新日期:2001-07-01 00:00:00

  • Murine influenza virus encephalomyelitis. III. Effect of defective interfering virus particles.

    abstract::Defective interfering influenza virus particles lessened the yield of infective virus recovered from brain after intracerebral challange of 3-week old mice, but failed to affect the appearance of disease or lethality. In 7-week old mice, the presence of defective interfering influenza virus particles reduced both leth...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00684666

    authors: Gamboa ET,Harter DH,Duffy PE,Hsu KC

    更新日期:1976-03-15 00:00:00

  • Immunocytochemical and ultrastructural studies of the motor cortex in amyotrophic lateral sclerosis.

    abstract::This report concerns an immunocytochemical and ultrastructural study of the motor cortices of 11 patients with amyotrophic lateral sclerosis (ALS). Specimens from 12 normal individuals served as controls. Antibodies against phosphorylated neurofilament (PNF; 200 kDa), ubiquitin, glial fibrillary acidic protein (GFAP) ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00293318

    authors: Sasaki S,Maruyama S

    更新日期:1994-01-01 00:00:00

  • Similar topographical distribution of neurofibrillary tangles in amyotrophic lateral sclerosis and parkinsonism-dementia complex in people living in the Kii peninsula of Japan suggests a single tauopathy.

    abstract::The presence of many neurofibrillary tangles (NFTs) in the central nervous system is a hallmark of amyotrophic lateral sclerosis (ALS) and parkinsonism-dementia complex (PDC) in people living in the Kii peninsula of Japan and in the island of Guam. To determine whether or not ALS and PDC are on a spectrum of a single ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-007-0197-6

    authors: Mimuro M,Kokubo Y,Kuzuhara S

    更新日期:2007-06-01 00:00:00

  • Upregulated expression of Fas and Fas ligand in brain through the spectrum of HIV-1 infection.

    abstract::Apoptosis of neurons and glial cells has been shown to occur in the brain of patients with the acquired immune deficiency syndrome (AIDS) and was postulated as contributing to brain atrophy and white matter damage in these patients. Since apoptotic events may be induced by the Fas-Fas ligand (FasL) system, we analyzed...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s004010051094

    authors: Elovaara I,Sabri F,Gray F,Alafuzoff I,Chiodi F

    更新日期:1999-10-01 00:00:00

  • Genetic Creutzfeldt-Jakob disease associated with the E200K mutation: characterization of a complex proteinopathy.

    abstract::The E200K mutation is the most frequent prion protein gene (PRNP) mutation detected worldwide that is associated with Creutzfeldt-Jakob disease (CJD) and thought to have overlapping features with sporadic CJD, yet detailed neuropathological studies have not been reported. In addition to the prion protein, deposition o...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-010-0713-y

    authors: Kovacs GG,Seguin J,Quadrio I,Höftberger R,Kapás I,Streichenberger N,Biacabe AG,Meyronet D,Sciot R,Vandenberghe R,Majtenyi K,László L,Ströbel T,Budka H,Perret-Liaudet A

    更新日期:2011-01-01 00:00:00

  • Expansion of the classification of FTLD-TDP: distinct pathology associated with rapidly progressive frontotemporal degeneration.

    abstract::Frontotemporal lobar degeneration with TDP-43 inclusions (FTLD-TDP) can typically be categorized into one of four distinct histopathologic patterns of TDP-43 pathology, types A to D. The strength of this histopathologic classification lies in the association between FTLD-TDP subtypes and various clinical and genetic f...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-017-1679-9

    authors: Lee EB,Porta S,Michael Baer G,Xu Y,Suh E,Kwong LK,Elman L,Grossman M,Lee VM,Irwin DJ,Van Deerlin VM,Trojanowski JQ

    更新日期:2017-07-01 00:00:00

  • Morphometrical reappraisal of motor neuron system of Pick's disease and amyotrophic lateral sclerosis with dementia.

    abstract::The conventional concept of Pick's disease does not distinguish Pick's disease with Pick bodies (Pick body disease, PBD) from Pick's disease without Pick bodies [lobar atrophy without Pick bodies, LA-PB(-)]. Recently, intraneuronal ubiquitin-positive inclusions (ub-inclusions), which are thought to be a hallmark of am...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-001-0513-5

    authors: Ikeda K,Akiyama H,Arai T,Ueno H,Tsuchiya K,Kosaka K

    更新日期:2002-07-01 00:00:00

  • Colony stimulating factor-1 potentiates neuronal survival in cerebral cortex ischemic lesion.

    abstract::The effect of the cytokine, colony stimulating factor-1 (CSF-1), on neuronal survival in cerebral cortex ischemic lesion was determined. Ischemic lesions were made in C3H/HeJ mice by disrupting blood vessels that penetrate the cerebral cortex from the pial-vascular plexus. Recombinant human colony stimulating factor 1...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s004010050550

    authors: Berezovskaya O,Maysinger D,Fedoroff S

    更新日期:1996-11-01 00:00:00

  • Neuronal accumulation of silver in brains of progeny from argyric rats.

    abstract::Using a photochemical method silver was demonstrated in the brains of 1-, 14-, and 45-day-old rats which had been exposed to silver on gestational days 18 and 19. In the brain tissue of new-born rats, silver was found in the lysosomes of neurons and astroglia. Minor changes in the anatomic distribution of silver were ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00691995

    authors: Rungby J,Danscher G

    更新日期:1983-01-01 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

  • Amyloid deposition in the nucleus basalis of Meynert complex: a topographic marker for degenerating cell clusters in Alzheimer's disease.

    abstract::The deficiency of the cholinergic cortical projection system arising in the different basal forebrain structures collectively referred to as nucleus basalis of Meynert complex is a constant finding in Alzheimer's disease, a disorder which is neuro-pathologically characterised by the appearance of three intracerebral f...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00690530

    authors: Arendt T,Taubert G,Bigl V,Arendt A

    更新日期:1988-01-01 00:00:00

  • Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins.

    abstract::Massive GGGGCC repeat expansion in the first intron of the gene C9orf72 is the most common known cause of familial frontotemporal lobar degeneration (FTLD) and amyotrophic lateral sclerosis (ALS). Despite its intronic localization and lack of an ATG start codon, the repeat region is translated in all three reading fra...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-013-1189-3

    authors: Mori K,Arzberger T,Grässer FA,Gijselinck I,May S,Rentzsch K,Weng SM,Schludi MH,van der Zee J,Cruts M,Van Broeckhoven C,Kremmer E,Kretzschmar HA,Haass C,Edbauer D

    更新日期:2013-12-01 00:00:00

  • Distinct neuronal subset reveals perikaryal immunostaining for synaptophysin (protein p38) in the striatum of rats.

    abstract::An immunoperoxidase technique was used to locate synaptophysin (protein p38), a major integral membrane glycoprotein of synaptic vesicles, in the rat brain. In addition to a diffuse distribution of nerve terminal stainings for synaptophysin appearing as numerous small puncta, the large-sized cells with spindled or pol...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00304146

    authors: Goto S,Korematsu K,Nagahiro S,Ushio Y

    更新日期:1993-01-01 00:00:00

  • Demyelinating peripheral neuropathy associated with hemophagocytic lymphohistiocytosis. An immuno-electron microscopic study.

    abstract::We report the case of an 11-year-old male who developed subacute diffuse polyradiculoneuropathy, associated with digestive symptoms and Epstein-Barr virus infection. Parental consanguinity was present. The laboratory findings including bone marrow smear were consistent with hemophagocytic lymphohistiocytosis (HLH). El...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-004-0897-0

    authors: De Armas R,Sindou P,Gelot A,Routon MC,Ponsot G,Vallat JM

    更新日期:2004-10-01 00:00:00

  • Ectopic neurones in the hippocampus of the postnatal rat exposed to methylazoxymethanol during foetal development.

    abstract::Ectopic neurons have been detected in the hippocampus of postnatal hooded rats aged 5-24 days. These rats were exposed to methylazoxymethanol acetate (MAMac) during foetal development by injecting the mother rats with this neurotoxin. At birth, the hippocampus of rats exposed to MAMac showed a normal cytoarchitecture;...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00688698

    authors: Singh SC

    更新日期:1977-10-10 00:00:00

  • Age-related plaque morphology and C-terminal heterogeneity of amyloid beta in Dutch-type hereditary cerebral hemorrhage with amyloidosis.

    abstract::The evolvement of amyloid beta (Abeta) deposition in the frontal cerebral cortex of 24 patients of increasing age with Dutch-type hereditary cerebral hemorrhage with amyloidosis (HCHWA-D) was studied using end-specific monoclonal antibodies to Abetax-42 (Abeta42) or Abetax-40 (Abeta40) and markers for degenerating neu...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s004010051143

    authors: Maat-Schieman ML,Yamaguchi H,van Duinen SG,Natté R,Roos RA

    更新日期:2000-04-01 00:00:00

  • Alanine formation and alanine aminotransferase activity in the nerve tissue with proliferating macroglia.

    abstract::In the nerve tissue with proliferating macroglia cells were observed a lowered oxygen consumption, an increased aerobic glycolysis and alanine formation and a higher alanine aminotransferase and glutamate dehydrogenase activity than in the control tissue in the homogenates and in the cell sap fraction. The substrate s...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00684665

    authors: Ruscák M,Hager H,Orlický J

    更新日期:1976-03-15 00:00:00

  • Evaluation of CD33 as a genetic risk factor for Alzheimer's disease.

    abstract::In 2011, genome-wide association studies implicated a polymorphism near CD33 as a genetic risk factor for Alzheimer's disease. This finding sparked interest in this member of the sialic acid-binding immunoglobulin-type lectin family which is linked to innate immunity. Subsequent studies found that CD33 is expressed in...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章,评审

    doi:10.1007/s00401-019-02000-4

    authors: Estus S,Shaw BC,Devanney N,Katsumata Y,Press EE,Fardo DW

    更新日期:2019-08-01 00:00:00

  • Loss of murine TDP-43 disrupts motor function and plays an essential role in embryogenesis.

    abstract::Abnormal TDP-43 aggregation is a prominent feature in the neuropathology of amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration. Mutations in TARDBP, the gene encoding TDP-43, cause some cases of ALS. The normal function of TDP-43 remains incompletely understood. To better understand TDP-43 biolo...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-010-0659-0

    authors: Kraemer BC,Schuck T,Wheeler JM,Robinson LC,Trojanowski JQ,Lee VM,Schellenberg GD

    更新日期:2010-04-01 00:00:00

  • Tumour cell migration in adamantinomatous craniopharyngiomas is promoted by activated Wnt-signalling.

    abstract::Activating beta-catenin mutations with aberrant cytoplasmic and nuclear protein accumulation are hallmarks of adamantinomatous craniopharyngiomas (adaCP). These tumours tend to be associated with unfavourable and occasionally disastrous sequelae, as they invade adjacent brain structures such as the hypothalamus. The p...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-010-0642-9

    authors: Hölsken A,Buchfelder M,Fahlbusch R,Blümcke I,Buslei R

    更新日期:2010-05-01 00:00:00