The molecular biology of senile plaques and neurofibrillary tangles in Alzheimer's disease.

Abstract:

:Since the earliest descriptions of the disease, senile plaques (SP) and neurofibrillary tangles (NFT) have been regarded as the pathological 'hallmarks' of Alzheimer's disease (AD). Whether or not SP and NFT are sufficient cause to explain the neurodegeneration of AD is controversial. The major molecular constituents of these lesions, viz., beta-amyloid (Ass) and tau, have played a defining role both in the diagnosis of the disease and in studies of pathogenesis. The molecular biology of SP and NFT, however, is complex with many chemical constituents. An individual constituent could be the residue of a pathogenic gene mutation, result from cellular degeneration, or reflect the acquisition of new proteins by diffusion and molecular binding. This review proposes that the molecular composition of SP and NFT is largely a consequence of cell degeneration and the later acquisition of proteins. Such a conclusion has implications both for the diagnosis of AD and in studies of disease pathogenesis.

journal_name

Folia Neuropathol

journal_title

Folia neuropathologica

authors

Armstrong RA

subject

Has Abstract

pub_date

2009-01-01 00:00:00

pages

289-99

issue

4

eissn

1641-4640

issn

1509-572X

pii

13830

journal_volume

47

pub_type

杂志文章,评审
  • [Glioblastoma with BRAFV600E mutation and numerous metastatic foci: a case report].

    abstract::Glioblastoma, the most malignant astrocytic tumour, is associated with limited survival and thus rare metastases. We analysed a particularly interesting case - a 51-year-old male diagnosed within 2 years with primary and recurrent glioblastoma, isocitrate dehydrogenase (IDH)-wild type, as well as with numerous extra-c...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:10.5114/fn.2019.83833

    authors: Janik K,Och W,Popeda M,Rosiak K,Peciak J,Rieske P,Kulbacki K,Szostak B,Parda A,Stoczynska-Fidelus E

    更新日期:2019-01-01 00:00:00

  • Risk factors for Alzheimer's disease.

    abstract::Early reviews identified over 20 risk factors associated with Alzheimer's disease (AD) including age, familial inheritance, exposure to aluminium, traumatic brain injury (TBI), and associated co-morbidities such as vascular disease and infection. In the light of recent evidence, this review reconsiders these risk fact...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章,评审

    doi:10.5114/fn.2019.85929

    authors: A Armstrong R

    更新日期:2019-01-01 00:00:00

  • The interaction between lung cancer metastases to the brain and their surroundings.

    abstract:BACKGROUND AND STUDY PURPOSE:due to the fact that an interrelation between metastases of lung cancer to the brain and surroundings may influence the prognosis, we made attempts to answer the following questions: 1) how is the border between the tumour and its surroundings formed? 2) are there any differences in the gli...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:

    authors: Tabaka J,Nowacki P,Pankowski J

    更新日期:2006-01-01 00:00:00

  • Effects of hypothermia on ex vivo microglial production of pro- and anti-inflammatory cytokines and nitric oxide in hypoxic-ischemic brain-injured mice.

    abstract:INTRODUCTION:Activated microglia produce neurotoxic factors, including pro-inflammatory cytokines and nitric oxide (NO), in response to neuronal destruction. Therapeutic suppression of microglial release of these factors by various approaches including hypothermia is considered to be neuroprotective after severe brain ...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:10.5114/fn.2014.43786

    authors: Matsui T,Kida H,Iha T,Obara T,Nomura S,Fujimiya T,Suzuki M

    更新日期:2014-01-01 00:00:00

  • Sporadic inclusion body myositis: clinical, pathological, and genetic analysis of eight Polish patients.

    abstract:INTRODUCTION:Sporadic inclusion body myositis (sIBM) is one of the most common myopathies in patients above 50 years of age. Its progressive course finally leads to immobilisation, and no effective therapy exists. Its pathogenesis includes both degenerative and inflammatory processes, however, its direct causes remain ...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:10.5114/fn.2015.56550

    authors: Kierdaszuk B,Berdynski M,Palczewski P,Golebiowski M,Zekanowski C,Kaminska AM

    更新日期:2015-01-01 00:00:00

  • Frontotemporal dementia and parkinsonism linked to chromosome 17.

    abstract::Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) is an autosomal dominant neurodegenerative disorder caused by mutations in the MAPT gene which encodes the microtubule-associated protein tau. This hereditary tauopathy is a rare clinical syndrome, affecting approximately two hundred kindreds a...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章,评审

    doi:

    authors: Wszołek ZK,Słowiński J,Golan M,Dickson DW

    更新日期:2005-01-01 00:00:00

  • Long-term effect of IFN-beta 1a therapy on CCL2 (MCP-1) chemokine in patients with multiple sclerosis.

    abstract::Chemokines play an important role in pathogenesis of multiple sclerosis (MS), mediating migration of leukocytes into the central nervous system. CCL2 (MCP-1) chemokine is expressed in astrocytes in MS lesions. The aim of the study was to evaluate the effect of a two-year treatment with IFN-beta 1a on serum CCL2 level ...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:

    authors: Szczuciński A,Losy J

    更新日期:2004-01-01 00:00:00

  • Reaction of microglial cells in human astrocytomas (preliminary report).

    abstract::Forty human primary brain tumors: twelve protoplasmic, six gemistocytic, four fibrillary and ten anaplastic astrocytomas, eight glioblastomas were submitted for immunohistochemical and histochemical characterization of microglia in tumor tissue and in its surroundings. The following antibodies were used: GFAP, ferriti...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:

    authors: Wierzba-Bobrowicz T,Kuchna I,Matyja E

    更新日期:1994-01-01 00:00:00

  • Krabbe disease: an ultrastructural study of globoid cells and reactive astrocytes at the brain and optic nerves.

    abstract::We report here a detailed ultrastructural study of a brain biopsy along with post-mortem brain and optic nerve specimens from a case of Krabbe disease, a relatively rare leukodystrophy caused by a mutation in the gene for galactocerebrosidase (GALC) mapped to the 14q31 region of chromosome 14. GALC is responsible for ...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:

    authors: Jesionek-Kupnicka D,Majchrowska A,Krawczyk J,Wendorff J,Barcikowska M,Lukaszek S,Liberski PP

    更新日期:1997-01-01 00:00:00

  • Ultrastructural changes in neuronal and glial cells in subacute sclerosing panencephalitis: correlation with disease duration.

    abstract::This paper presents ultrastructural changes in neuronal and glial cells with special reference to intranuclear inclusion bodies in subacute sclerosing panencephalitis (SSPE) with different duration (from several weeks to seven years). Brain autopsy at ultrastructural level revealed the nucleocapsids of paramyxovirus i...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:

    authors: Lewandowska E,Szpak GM,Lechowicz W,Pasennik E,Sobczyk W

    更新日期:2001-01-01 00:00:00

  • Opportunistic infections of the central nervous system in the course of acquired immune deficiency syndrome (AIDS). Morphological analysis of 172 cases.

    abstract::A neuropathological analysis of 172 cases of AIDS in adults was carried out, to determine the occurrence and nature of the opportunistic infections of the central nervous system (CNS). The material comprised 155 cases of men, and 17 women. Mean age of patients was 38 years. Collection under study originated from the p...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:

    authors: Zelman IB,Mossakowski MJ

    更新日期:1998-01-01 00:00:00

  • The significance of immunocytochemical markers, synaptophysin and neurofilaments in diagnosis of ganglioglioma.

    abstract::Ganglioglioma is a tumor composed of neoplastic neurons and neoplastic glial cells mixed in different proportions. Astrocytes are the essential glial component. The tumor proliferates mostly in the temporal lobe cortex, scarcely in other areas of the brain. In ganglioglioma the population of ganglionic neurons is very...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:

    authors: Wierzba-Bobrowicz T,Schmidt-Sidor B,Gwiazda E,Bertrand E

    更新日期:1999-01-01 00:00:00

  • Clinicopathological and ultrastructural study in two cases of chordoid glioma.

    abstract::Chordoid glioma is a rare benign neoplasm of uncertain histogenesis occurring in the third ventricle/ /suprasellar region. Recently, data have emerged suggesting that chordoid glioma is a variant of ependymoma related to a specialised ependyma of the subcommisural organ or the lamina terminalis area. In this study, we...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:

    authors: Taraszewska A,Bogucki J,Andrychowski J,Koszewski W,Czernicki Z

    更新日期:2003-01-01 00:00:00

  • Necrobiosis lipoidica and cutaneous anaesthesia: immunohistochemical study of neural fibres.

    abstract:BACKGROUND:Cutaneous anaesthesia in necrobiosis lipoidica (NL) has been attributed to the destruction of nerve fibres by the inflammatory process. In the 1980s, one study demonstrated a decrease in S100 positive neural fibres as proof of this. Thermalgic information is mainly dependent on small fibres, either myelinate...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:

    authors: Fernandez-Flores A

    更新日期:2008-01-01 00:00:00

  • Diagnostic difficulties in Krabbe disease: a report of two cases and review of literature.

    abstract::Globoid cell leukodystrophy (GLD, also known as Krabbe disease), whose pathophysiology is still not completely elucidated, is an inherited, metabolic, and neurodegenerative disease, caused by the deficiency of β-galactocerebrosidase (GALC) or in very rare cases by lack of active saposin A. We describe two patients, i...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章,评审

    doi:10.5114/fn.2012.32364

    authors: Szymańska K,Ługowska A,Laure-Kamionowska M,Bekiesińska-Figatowska M,Gieruszczak-Białek D,Musielak M,Eichler S,Giese AK,Rolfs A

    更新日期:2012-01-01 00:00:00

  • CCL2 (MCP-1) and CCL5 (RANTES) levels in the peripheral blood of multiple sclerosis patients treated with Glatiramer Acetate (Copaxone).

    abstract::The MCP-1 and RANTES levels were measured in 20 multiple sclerosis patients before and after 1 year daily treatment with 20 mg of subcutaneously applied glatiramer acetate. The level of MCP-1 in serum from multiple sclerosis patients was lower than in control subjects. After one year of therapy with glatiramer acetate...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:

    authors: Losy J,Michałowska-Wender G,Kurdyńska A,Wender M

    更新日期:2005-01-01 00:00:00

  • Neuroacanthocytosis. Review of literature and case report.

    abstract::Neuroacanthocytosis is a rare disease of nervous system with multisystem pathology. This review presents clinical syndromes and morphological changes of sporadic and familial forms of neuroacanthocytosis and is illustrated by the case of a 27-year-old man. Progressive extrapyramidal syndrome appeared at the age of 22....

    journal_title:Folia neuropathologica

    pub_type: 杂志文章,评审

    doi:

    authors: Rafałowska J,Drac H,Jamrozik Z

    更新日期:1996-01-01 00:00:00

  • Recurrent cerebral infarcts as the first manifestation of infection with the HIV virus.

    abstract::There is an increased risk of stroke in patients with HIV infection. One of the mechanisms is production of anticardiolipin (aCL) antibodies, induced by the virus. Many studies have documented a high incidence of aCL antibodies in patients with HIV infection and the increased risk of stroke, although there is no such ...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:

    authors: Gorczyca I,Stanek M,Podlasin B,Furmanek M,Pniewski J

    更新日期:2005-01-01 00:00:00

  • Evaluation of survival and maturation of cryopreserved dopaminergic fetal cells transplanted into rat striatum and an analysis of the host brain reaction to graft.

    abstract::A fetal, cryopreserved ventral mesencephalic rat tissue was transplanted into striatum of healthy adult rats. A stereotactic apparatus was used for transplantation of solid tissue blocks. The survival of transplanted dopaminergic cells in rat striatum was evaluated by means of histological and immunocytochemical metho...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:

    authors: Kosno-Kruszewska E,Wierzba-Bobrowicz T,Ilnicki K,Lechowicz W,Dymecki J

    更新日期:1996-01-01 00:00:00

  • Neuropathological variants of cystic encephalopathy in infants.

    abstract::The aim of our study was to present six cases with cystic changes within the white matter in infant brains and discuss the variants of this type of neuropathological lesions of the developing brain. Two of them exhibited the changes characteristic for cystic leucoencephalopathy. To the others with moderate involvement...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:

    authors: Dambska M,Kuchna I,Nowicki K

    更新日期:1994-01-01 00:00:00

  • Blood-brain barrier breakdown and cerebellar degeneration in the course of experimental neoplastic disease. Are circulating Cytokine-Induced Neutrophil Chemoattractant-1 (CINC-1) and -2alpha(CINC-2alpha) the involved mediators?

    abstract::Cerebellar degeneration belongs to indirect effects of malignancy on the nervous system. Although the involvement of immune system is accepted as a hypothesis of its pathology, the clinical observations of ineffective immunomodulatory therapy suggest complex pathomechanisms, which await elucidation. The aim of this st...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:

    authors: Michalak S,Wender M,Michalowska-Wender G,Kozubski W

    更新日期:2010-01-01 00:00:00

  • Recombinant forms of myelin antigens expressed on Chinese hamster ovary (CHO) cells as a tool for identification of autoantibodies in serum of multiple sclerosis patients.

    abstract::A contribution of B cells and autoantibodies has been demonstrated in MS leading to interest in the use of such autoantibodies as diagnostic or prognostic markers and as a basis for immunomodulatory therapy. ELISA and Western fail to detect reactivity against epitopes displayed by native antigens expressed on myelin s...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:

    authors: Jaśkiewicz E,Michałowska-Wender G,Pyszczek A,Wender M

    更新日期:2010-01-01 00:00:00

  • Morphology of pineal glands in human foetuses and infants with brain lesions.

    abstract::The pineal gland is an organ involved in regulation of homeostasis and body rhythms. It plays an important role in the growth foetuses and adaptation of newborns to new environmental conditions. The requirements of foetuses and newborns progressively change during development. The purpose of the study was to evaluate ...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:

    authors: Laure-Kamionowska M,Maślińska D,Deregowski K,Czichos E,Raczkowska B

    更新日期:2003-01-01 00:00:00

  • Neurodegenerative disease in infants with multiple congenital malformations--report of two cases.

    abstract::During embryogenesis, about 40% of genes are involved in the development of the central nervous system (CNS). The same genes support the integrity and function of brain cells in humans. Birth defects cause different changes in genetic material during embryogenesis. They may also be responsible for precocious death of ...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:

    authors: Schmidt-Sidor B,Mierzewska H,Turzyniecka M,Kowalewska-Kantecka B,Wierzba-Bobrowicz T,Lechowicz W

    更新日期:2004-01-01 00:00:00

  • HTLV-I-associated myelopathy/tropical spastic paraparesis (HAM/TSP): the role of HTLV-I-infected Th1 cells in the pathogenesis, and therapeutic strategy.

    abstract::Human T lymphotropic virus type I (HTLV-I)-associated myelopathy/tropical spastic paraparesis (HAM/TSP) is a chronic progressive myelopathy characterized by bilateral pyramidal tract involvement with sphincteric disturbances. The primary neuropathological feature of HAM/TSP is chronic myelitis characterized by perivas...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章,评审

    doi:

    authors: Nakamura T

    更新日期:2009-01-01 00:00:00

  • Submicroscopic pathology of human and experimental hydrocephalic cerebral cortex.

    abstract::The ultrastructural pathology of cerebral cortex in human hydrocephalus is reviewed and compared with experimental hydrocephalus. Nerve cells show moderate and severe swelling. The neighboring neuropil exhibits notable enlargement of extracellular space, synaptic plasticity and degeneration, damage of myelinated axons...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章,评审

    doi:

    authors: Castejón OJ

    更新日期:2010-01-01 00:00:00

  • Erk activation as a possible mechanism of transformation of subependymal nodule into subependymal giant cell astrocytoma.

    abstract:INTRODUCTION:Subependymal nodule (SEN) and subependymal giant cell astrocytoma (SEGA) are brain lesions frequently found in tuberous sclerosis (TS). As about 10-15% of SENs enlarge and transform into SEGAs, we examined here the possible mechanism of the phenomenon. MATERIAL AND METHODS:Using Western blot we studied 1 ...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:10.5114/fn.2015.49969

    authors: Siedlecka M,Szlufik S,Grajkowska W,Roszkowski M,Jóźwiak J

    更新日期:2015-01-01 00:00:00

  • Supratentorial astrocytoma associated with arteriovenous malformation. Case report.

    abstract::A case of the 18-year-old boy suffering from epilepsy since 8 years and suspected of microangioma is presented. The craniotomy revealed left parietal parasagittal superficially located neoplasm and arteriovenous malformation beneath. Unexpected fibrillary astrocytoma associated with vascular tumor was the diagnostic p...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:

    authors: Kroh H,Bidziński J,Majchrowski A

    更新日期:1994-01-01 00:00:00

  • Clinical presentation of Y189C mutation of the NOTCH3 gene in the Polish family with CADASIL.

    abstract:INTRODUCTION:Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary, progressive ischemic disease of small vessels of the brain characterized by migraine with aura (MA), recurrent subcortical ischemic episodes, cognitive decline and psychiatric disorders. CA...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:10.5114/fn.2020.94009

    authors: Dorszewska J,Kowalska M,Grzegorski T,Dziewulska D,Karmelita-Katulska K,Barciszewska AM,Prendecki M,Gorczyński W,Kozubski W

    更新日期:2020-01-01 00:00:00

  • Does lipopolysaccharide-based neuroinflammation induce microglia polarization?

    abstract::Lipopolysaccharide (LPS) is a potent immunogen when administered locally and/or systemically. The peripheral immunization with LPS could contribute to the progression of neurological diseases because a strong link between neuroinflammation and dopaminergic degeneration has been found. The switch between the survival a...

    journal_title:Folia neuropathologica

    pub_type: 杂志文章

    doi:10.5114/fn.2020.96755

    authors: Hernandez Baltazar D,Nadella R,Barrientos Bonilla A,Flores Martínez Y,Olguín A,Heman Bozadas P,Rovirosa Hernández M,Cibrián Llanderal I

    更新日期:2020-01-01 00:00:00