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 lumens. They were not observed in the pericytes or stromal cells. They were round to polygonal, 0.5-1.0 micron in size and composed of substructural units of parallel thick and thin electron-dense lines with a periodicity of 180-220 A. They coexisted occasionally with Weibel-Palade bodies but shared no structural correlation with them. The nature and significance of these crystalloid bodies are as yet unknown. Their close association with pinocytic vesicles suggests that the substructural crystalline might be the result of reconstruction of absorbed material from either the vascular lumen or the interstitium. Their subsequent development, associated with lysosomal activity, into intracytoplasmic dense bodies is postulated. Since crystalloid bodies were found only in endothelial cells, particularly those active in proliferation, they may play a pathophysiologic role in relation to angiogenesis.

journal_name

Acta Neuropathol

journal_title

Acta neuropathologica

authors

Ho KL

doi

10.1007/BF00688686

subject

Has Abstract

pub_date

1985-01-01 00:00:00

pages

117-26

issue

2

eissn

0001-6322

issn

1432-0533

journal_volume

66

pub_type

杂志文章
  • Spinal neuronal pathology associated with continuous intrathecal infusion of N-methyl-D-aspartate in the rat.

    abstract::Continuous intrathecal infusion of N-methyl-D-aspartate (NMDA) at the level of the lumbar enlargement of the spinal cord in middle-aged rats produced dose-dependent toxicity of spinal cord neuronal systems. Toxicity was enhanced by coadministration of glycine, but was significantly reduced when NMDA was co-administere...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00662631

    authors: Nag S,Riopelle RJ

    更新日期:1990-01-01 00:00:00

  • Identification of components of immunoglobulins in senile plaques by means of fluorescent antibody technique.

    abstract::Using a fluorescent antibody technique, sections of the brains of patients with senile dementia or Alzheimer's disease containing senile plaques were treated with rabbit antihuman immunoglobulins labelled with FITC (fluorescein isothiocyanate, BBL). The senile plaques and the cerebral amyloid angiopathy (drusige Entar...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00689569

    authors: Ishii T,Haga S

    更新日期:1975-08-11 00:00:00

  • Flow cytometric analysis of the DNA distribution in human brain tumors.

    abstract::Flow cytofluorometric analysis was used to determine the distribution of the DNA content in cells from selected areas of normal human brain and in benign and malignant brain tumors. Propidium iodide was employed as DNA fluorochrome and the analysis was carried out on a suspension of single cells. Normal, nonstimulated...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00684802

    authors: Kawamoto K,Herz F,Wolley RC,Hirano A,Kajikawa H,Koss LG

    更新日期:1979-04-12 00:00:00

  • [The effect of blood-filled meshwork of arachnoid villi in connection with posttraumatic brain edema (author's transl)].

    abstract::Based on the Kellie-Munro doctrine according to which the intracranial compartments--blood, brain, and CSF--are in a state of pressure and volume equilibrium, we examined if traumatic lesions of the liquor absorption passages could change the intracranial pressure (ICP). Therefore, we reviewed the arachnoid villi and ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00691896

    authors: Dirnhofer R,Sigrist T

    更新日期:1979-02-15 00:00:00

  • Exertional rhabdomyolysis and exercise intolerance revealing dystrophinopathies.

    abstract::Exercise intolerance associated with myalgias, muscle cramps or myoglobinuria may be associated with a dystrophinopathy. A search for abnormal dystrophin expression (using immunohistochemistry, immunoblot and DNA analysis) was carried out in a series of 15 patients. They were selected because they presented exercise i...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s004010050671

    authors: Figarella-Branger D,Baeta Machado AM,Putzu GA,Malzac P,Voelckel MA,Pellissier JF

    更新日期:1997-07-01 00:00:00

  • Progressive accumulation of ubiquitin and disappearance of alpha-synuclein epitope in multiple system atrophy-associated glial cytoplasmic inclusions: triple fluorescence study combined with Gallyas-Braak method.

    abstract::Alpha-synuclein (alphaS) and ubiquitin (Ub) are shared constituents of glial cytoplasmic inclusions (GCIs) and Lewy bodies (LBs), both composed of fibrillary structures. Staining profiles of GCIs were investigated with triple immunofluorescence involving immunostaining for alphaS and Ub, both amplified with catalyzed ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-005-1066-9

    authors: Sakamoto M,Uchihara T,Nakamura A,Mizutani T,Mizusawa H

    更新日期:2005-10-01 00:00:00

  • Differential radiosensitivity of neurons and neuroglia of the hippocampus in the adult rabbit.

    abstract::Adult rabbits were subjected to 4.5 Gy of whole-blody or brain alone gamma-irradiation, and their hippocampus was examined with the light and electron microscope. Pycnotic cells were found at the base of the granular layer of the dentate gyrus in the so-called subgranular zone, as soon as 3 h after irradiation, and we...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00690520

    authors: Guéneau G,Drouet J,Privat A,Court L

    更新日期:1979-12-01 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

  • Investigation on the expression of major histocompatibility complex class II and cytokines and detection of HIV-1 DNA within brains of asymptomatic and symptomatic HIV-1-positive patients.

    abstract::Among the various mechanisms proposed to explain the pathogenesis of cerebral lesions in human immunodeficiency virus (HIV)-induced encephalitis, a cytokine-mediated action has found most favour. Indeed, elevated expression of cytokines such as interleukin (IL)-1 and tumor necrosis factor-alpha (TNF-alpha), thought to...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s004010050457

    authors: An SF,Ciardi A,Giometto B,Scaravilli T,Gray F,Scaravilli F

    更新日期:1996-01-01 00:00:00

  • K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas.

    abstract::Pediatric glioblastomas (GBM) including diffuse intrinsic pontine gliomas (DIPG) are devastating brain tumors with no effective therapy. Here, we investigated clinical and biological impacts of histone H3.3 mutations. Forty-two DIPGs were tested for H3.3 mutations. Wild-type versus mutated (K27M-H3.3) subgroups were c...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-012-0998-0

    authors: Khuong-Quang DA,Buczkowicz P,Rakopoulos P,Liu XY,Fontebasso AM,Bouffet E,Bartels U,Albrecht S,Schwartzentruber J,Letourneau L,Bourgey M,Bourque G,Montpetit A,Bourret G,Lepage P,Fleming A,Lichter P,Kool M,von Deimling

    更新日期:2012-09-01 00:00:00

  • Transplacental effect of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) on brain dopaminergic neurons in the mouse. An immunohistochemical study.

    abstract::Immunohistochemical studies of monoamine neurons were performed to evaluate toxic effects of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) on young adult mice and compare them with those of their offspring. Mice, 9-11 weeks old (C57BL/6J), injected subcutaneously with a large dose of MPTP (17 mg/kg per day) duri...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00294662

    authors: Furune S,Miura K,Watanabe K,Nagao S,Takahashi H,Sakai M,Spatz M,Nagatsu I

    更新日期:1989-01-01 00:00:00

  • Adrenomyeloneuropathy. A protracted, pseudosystematic variant of adrenoleukodystrophy.

    abstract::Histopathological, immunocytochemical, and electron microscopical investigations were carried out in a man with a protracted history of spastic paraparesis, adrenal insufficiency and hypogonadism. Pathological findings were identical with those of the few previously reported cases of adrenomyeloneuropathy (AMN) includ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00690750

    authors: Probst A,Ulrich J,Heitz PU,Herschkowitz N

    更新日期:1980-01-01 00:00:00

  • Histochemical localization of aluminum in the rabbit CNS.

    abstract::Aluminum was observed in the nucleolus, interchromatin granules, rough endoplasmic reticulum, free ribosomes, euchromatin, and the heterochromatin of the neuron. The association of aluminum with the first four r-RNA-containing cellular components and with the last two DNA-containing chromatins suggests the association...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00690191

    authors: Wen GY,Wisniewski HM

    更新日期:1985-01-01 00:00:00

  • Impairment of axonal transport in the axon hillock and the initial segment of anterior horn neurons in transgenic mice with a G93A mutant SOD1 gene.

    abstract::Impaired axonal transport of the fast or slow component has been reported in patients with sporadic amyotrophic lateral sclerosis (ALS), animal models for ALS, and familial ALS-linked mutant Cu/Zn superoxide dismutase (SOD1) transgenic mice. However, little is known about the impairment of axonal transport in mutant S...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-005-1021-9

    authors: Sasaki S,Warita H,Abe K,Iwata M

    更新日期:2005-07-01 00:00:00

  • Optic nerve axonal pathology is related to abnormal visual evoked responses in AIDS.

    abstract::Electrophysiological studies in subjects with HIV/AIDS demonstrate subtle changes in the visual pathway even in the absence of visual symptoms. But the pathological correlate of the electrophysiological abnormalities is largely unknown. This study attempts to correlate pathological changes in the retina and intraorbit...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-006-0089-1

    authors: Mahadevan A,Satishchandra P,Prachet KK,Sidappa NB,Ranga U,Santosh V,Yasha TC,Desai A,Ravi V,Shankar SK

    更新日期:2006-10-01 00:00:00

  • Relationship of adjuvants and swine influenza vaccine to experimental neuropathy in rabbits.

    abstract::Experimental neuropathy, characterized by endoneurial edema and demyelination, was induced by inoculating rabbits with a combination of Freund's complete adjuvant (FCA), gangliosides, lecithin and cholesterol. A less severe demyelinating neuropathy could be induced by treatment with FCA alone but no significant change...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00695496

    authors: Powell HC,Mizisin AP,Wiley CA,Morey MK,Hughes RA

    更新日期:1987-01-01 00:00:00

  • Mutation analysis of hBUB1, hBUBR1 and hBUB3 genes in glioblastomas.

    abstract::Glioblastomas, the most malignant human brain tumors, are characterized by marked aneuploidy, suggesting chromosomal instability which may be caused by a defective mitotic spindle checkpoint. We screened 22 glioblastomas for mutations in the mitotic spindle check-point genes hBUB1, hBUBR1 and hBUB3. DNA sequencing rev...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s004010100366

    authors: Reis RM,Nakamura M,Masuoka J,Watanabe T,Colella S,Yonekawa Y,Kleihues P,Ohgaki H

    更新日期:2001-04-01 00:00:00

  • Myopathy in Marinesco-Sjögren syndrome links endoplasmic reticulum chaperone dysfunction to nuclear envelope pathology.

    abstract::Marinesco-Sjögren syndrome (MSS) features cerebellar ataxia, mental retardation, cataracts, and progressive vacuolar myopathy with peculiar myonuclear alterations. Most MSS patients carry homozygous or compound heterozygous SIL1 mutations. SIL1 is a nucleotide exchange factor for the endoplasmic reticulum resident cha...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-013-1224-4

    authors: Roos A,Buchkremer S,Kollipara L,Labisch T,Gatz C,Zitzelsberger M,Brauers E,Nolte K,Schröder JM,Kirschner J,Jesse CM,Goebel HH,Goswami A,Zimmermann R,Zahedi RP,Senderek J,Weis J

    更新日期:2014-05-01 00:00:00

  • Neuronal loss in the basal nucleus of Meynert in progressive supranuclear palsy.

    abstract::A morphometric study of the basal nucleus of Meynert (bnM) has been performed in a 70-year-old man with a 4-year history of pathologically confirmed progressive supranuclear palsy (PSP). An important neuronal loss (52%) was demonstrated in the bnM. This finding has not been previously documented with morphometric meth...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00697397

    authors: Tagliavini F,Pilleri G,Gemignani F,Lechi A

    更新日期:1983-01-01 00:00:00

  • Peripheral nerve axonal dwindling with concomitant myelin sheath hypertrophy in experimentally induced diabetes.

    abstract::Axons of the peripheral nervous system (PNS) are reduced in caliber in response to the experimental diabetic state. The cause of this reduced axonal size is disputed. Various theories include (a) axonal dwindling, (b) inhibition of growth, and (c) shrinkage due to serum hyperosmolarity. This study was designed to dire...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00688637

    authors: Mattingly GE,Fischer VW

    更新日期:1985-01-01 00:00:00

  • Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease.

    abstract::Frontotemporal lobar degeneration with TAR DNA-binding protein 43 inclusions (FTLD-TDP) is the most common pathology associated with frontotemporal dementia (FTD). Repeat expansions in chromosome 9 open reading frame 72 (C9ORF72) and mutations in progranulin (GRN) are the major known genetic causes of FTLD-TDP; howeve...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-015-1436-x

    authors: Pottier C,Bieniek KF,Finch N,van de Vorst M,Baker M,Perkersen R,Brown P,Ravenscroft T,van Blitterswijk M,Nicholson AM,DeTure M,Knopman DS,Josephs KA,Parisi JE,Petersen RC,Boylan KB,Boeve BF,Graff-Radford NR,Veltman JA

    更新日期:2015-07-01 00:00:00

  • Pathological proteins Tau 64 and 69 are specifically expressed in the somatodendritic domain of the degenerating cortical neurons during Alzheimer's disease. Demonstration with a panel of antibodies against Tau proteins.

    abstract::Bundles of paired helical filaments (PHF) accumulate in the pyramidal neurons that degenerate during Alzheimer's disease. This neurofibrillary degeneration is highly correlated with clinical signs of dementia. During the degenerating process, Tau proteins, which are the major antigenic components of PHF, are abnormall...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00308912

    authors: Delacourte A,Flament S,Dibe EM,Hublau P,Sablonnière B,Hémon B,Shérrer V,Défossez A

    更新日期:1990-01-01 00:00:00

  • Silver diagnosis in neuropathology: principles, practice and revised interpretation.

    abstract::Silver-staining methods are helpful for histological identification of pathological deposits. In spite of some ambiguities regarding their mechanism and interpretation, they are widely used for histopathological diagnosis. In this review, four major silver-staining methods, modified Bielschowsky, Bodian, Gallyas (GAL)...

    journal_title:Acta neuropathologica

    pub_type: 历史文章,杂志文章,评审

    doi:10.1007/s00401-007-0200-2

    authors: Uchihara T

    更新日期:2007-05-01 00:00:00

  • A new neurophysiological/neuropathological ex vivo model localizes the origin of glioma-associated epileptogenesis in the invasion area.

    abstract::Seizures commonly occur in glioma patients, but their pathogenesis is poorly understood, in part due to a lack of valid and versatile experimental models. We have established a new model that enables comprehensive neuropathological and neurophysiological analysis on identical tissue preparations. Rat C6 glioma cells s...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-003-0771-5

    authors: Senner V,Köhling R,Püttmann-Cyrus S,Straub H,Paulus W,Speckmann EJ

    更新日期:2004-01-01 00:00:00

  • Effects of methylmercury on neuroepithelial germinal cells in the developing telencephalic vesicles of mice.

    abstract::Methylmercury (MeHg) poisoning (20 mg/kg body weight) in embryonic mice resulted in significant reductions of mitotic indices in the neuroepithelial germinal cells of the telencephalon at the ventricular surface 4 to 12 h following intoxication. After 24 h, no significant difference in the mitotic indices was observed...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00293454

    authors: Choi BH

    更新日期:1991-01-01 00:00:00

  • [Myelinopathy due to carbon monoxyde poisoning. A study in ultrastructural neuropathology (author's transl)].

    abstract::A 24-year-old woman was found comatose after 2 days of cephalalgia and vomiting. An immediate diagnosis of carbon monoxyde poisoning was disclaimed when blood carbon monoxyde was found to be 1.75 ml/100. A diagnosis of acute intracranial hypertension led to trephination with ventricular punction and brain biopsy on th...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00685010

    authors: Foncin JF,Le Beau J

    更新日期:1978-08-07 00:00:00

  • Folliculo-stellate cell adenoma of the pituitary. A light- and electron-microscopic study.

    abstract::An unusual tumor of the pituitary gland is reported. The most characteristic finding of the present tumor was the presence of numerous "colloid" and mucoid secretions. The cells were stellate in shape and there were intra- or intercellular lumina which were lined by many microvilli and occasional cilia. There were als...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00687617

    authors: Yagishita S,Itoh Y,Nakazima S,Suzuki N,Hirata K,Yamashita T

    更新日期:1984-01-01 00:00:00

  • Effects of an intratumoral injection of human recombinant tumor necrosis factor-alpha on cerebrovascular permeability and leukocytic infiltration in a rat glioma model.

    abstract::The pro-inflammatory and blood-brain barrier (BBB) effects of intratumoral (IT) injection of human recombinant tumor necrosis factor-alpha (rTNF-alpha) were studied in the Fischer rat RT-2 glioma model. Animals received a single stereotaxic injection of either 6 x 10(4) U rTNF-alpha or excipient (vehicle) into the cen...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/pl00007398

    authors: Wright JL,Merchant RE

    更新日期:1997-01-01 00:00:00

  • Protracted form of Canavan's disease: case history and protein kinase activity of membrane fractions.

    abstract::Clinical and morphological findings in an 8-year-old Jewish girl with spongy leukodystrophy are presented. Ultrastructural changes indicated that this may be a form of Canavan's disease with some atypical features. Biochemical measurements indicated that synaptosomal membranes prepared from the striatum but not from t...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00691321

    authors: Boehme DH,Marks N

    更新日期:1981-01-01 00:00:00

  • Development of polyclonal antibodies and evaluation of a sensitive radioimmunoassay for detection and measurement of synaptophysin.

    abstract::Polyclonal antibodies directed towards synaptophysin were raised against a synthesised peptide corresponding to amino acids 246 to 260 of the human synaptophysin sequence. The antibodies, when applied for immunocytochemical staining, showed a staining pattern identical to that of the commercially available monoclonal ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00293325

    authors: Stridsberg M,Lundqvist G,Engström U,Wilander E,Su H,Gobl A,Oberg K

    更新日期:1994-01-01 00:00:00