The development of human fetal dorsal root ganglia in vitro: the first 20 days.

Abstract:

:Human fetal dorsal root ganglia aged from 8 to 12 weeks post-menstrual were grown in vitro for up to 20 days. Outgrowth of Schwann cells, axons and fibroblasts occurred after 4 h. By the 7th day in vitro Schwann cells enclosed bundles of axons and after 10 days some Schwann cells were seen to enclose individual axons. By the 20th day in vitro there was still a predominance of Schwann cells enclosing axonal bundles, but there were more individual axons ensheathed by three or four turns of Schwann cells. This arrangement mimics the early development in vivo of human dorsal root ganglia and provides the potential for an experimental system utilizing human nervous tissue rather than non-human animal models.

authors

Crawford K,Armati-Gulson P

doi

10.1111/j.1365-2990.1982.tb00315.x

subject

Has Abstract

pub_date

1982-11-01 00:00:00

pages

477-88

issue

6

eissn

0305-1846

issn

1365-2990

journal_volume

8

pub_type

杂志文章
  • MHC class II expression by microglia in tetanus toxin-induced experimental epilepsy in the rat.

    abstract::Minute amounts of tetanus toxin injected into the hippocampus of rats results in an epileptiform syndrome. When the toxin injection is made unilaterally or bilaterally into the ventral hippocampus, about one-third of animals with seizures show bilateral neuronal loss in dorsal CA1 of the hippocampus after 1 week. In a...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1111/j.1365-2990.1994.tb00985.x

    authors: Shaw JA,Perry VH,Mellanby J

    更新日期:1994-08-01 00:00:00

  • Review: Mechanistic target of rapamycin (mTOR) pathway, focal cortical dysplasia and epilepsy.

    abstract::Over the last decade, there has been increasing evidence that hyperactivation of the mechanistic target of rapamycin (mTOR) pathway is a hallmark of malformations of cortical development such as focal cortical dysplasia (FCD) or hemimegalencephaly. The mTOR pathway governs protein and lipid synthesis, cell growth and ...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章,评审

    doi:10.1111/nan.12463

    authors: Marsan E,Baulac S

    更新日期:2018-02-01 00:00:00

  • Changes of 5'-nucleotidase activity in cultured glioma cells.

    abstract::Changes of 5'-nucleotidase (5'-N) activity during subcultivation of C6 clonal rat glioma cells were studied histochemically, cytochemically and biochemically. Two different cell populations were seeded with high or low cell density respectively. 5'-N activity in cultured cells increased continuously in both population...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1111/j.1365-2990.1985.tb00014.x

    authors: Amano S,Sasahara M,Yamada E,Kataoka H,Hazama F

    更新日期:1985-05-01 00:00:00

  • Effect of ammonia on ciliary neurotrophic factor mRNA and protein expression and its upstream signalling pathway in cultured rat astroglial cells: possible implication of c-fos, Sp1 and p38MAPK.

    abstract::Ciliary neurotrophic factor (CNTF) may be implicated in the pathogenetic mechanisms of hepatic encephalopathy. We tested this hypothesis by treating confluent primary cultures of rat astroglial cells with ammonium chloride for various periods and analysing the effect of ammonia on the signalling pathway that regulates...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1111/j.1365-2990.2007.00831.x

    authors: Bodega G,Suárez I,Almonacid L,Ciordia S,Beloso A,López-Fernández LA,Zaballos A,Fernández B

    更新日期:2007-08-01 00:00:00

  • Distribution of tangles and threads in the cerebral cortex in progressive supranuclear palsy.

    abstract::Recent studies have described silver- and tau-positive glia and threads in the degenerating lesions of progressive supranuclear palsy. In this study, Gallyas-Braak silver impregnation and several immunohistochemical techniques were employed to examine the distribution of tangles, abnormal glia and threads in the cereb...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1111/j.1365-2990.1995.tb01066.x

    authors: Hanihara T,Amano N,Takahashi T,Nagatomo H,Yagashita S

    更新日期:1995-08-01 00:00:00

  • Neuronal DNA damage response-associated dysregulation of signalling pathways and cholesterol metabolism at the earliest stages of Alzheimer-type pathology.

    abstract:AIMS:Oxidative damage and an associated DNA damage response (DDR) are evident in mild cognitive impairment and early Alzheimer's disease, suggesting that neuronal dysfunction resulting from oxidative DNA damage may account for some of the cognitive impairment not fully explained by Alzheimer-type pathology. METHODS:Fr...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1111/nan.12252

    authors: Simpson JE,Ince PG,Minett T,Matthews FE,Heath PR,Shaw PJ,Goodall E,Garwood CJ,Ratcliffe LE,Brayne C,Rattray M,Wharton SB,MRC Cognitive Function and Ageing Neuropathology Study Group.

    更新日期:2016-02-01 00:00:00

  • A cortical microvascular structure in vascular dementia, Alzheimer's disease, frontotemporal lobar degeneration and nondemented controls: a sign of angiogenesis due to brain ischaemia?

    abstract:AIMS:We observed a microvascular structure in the cerebral cortex that has not, to our knowledge, been previously described. We have termed the structure a 'raspberry', referring to its appearance under a bright-field microscope. We hypothesized that raspberries form through angiogenesis due to some form of brain ischa...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1111/nan.12552

    authors: Ek Olofsson H,Englund E

    更新日期:2019-10-01 00:00:00

  • Neural tissue grafts and repair of the injured spinal cord.

    abstract::Neural tissue grafting presently stands as one of the more intriguing experimental strategies being applied to the problem of spinal cord regeneration. The following annotation presents an overview of recent investigations which have shown: that peripheral nerve grafts can stimulate axonal outgrowth in many descending...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1365-2990.1985.tb00007.x

    authors: Reier PJ

    更新日期:1985-03-01 00:00:00

  • Viliuisk encephalomyelitis--review of the spectrum of pathological changes.

    abstract::Viliuisk encephalomyelitis (VE) is an unique neurological disease occurring in the Iakut (Sakha) people of Siberia. Evolution of the disease follows one of three broad clinical forms: subacute, slowly progressive or chronic. Death occurs within 3 to 6 months in subacute cases and within 6 years in the slowly progressi...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:

    authors: McLean CA,Masters CL,Vladimirtsev VA,Prokhorova IA,Goldfarb LG,Asher DM,Vladimirtsev AI,Alekseev VP,Gajdusek DC

    更新日期:1997-06-01 00:00:00

  • Hirano body-rich subtypes of Creutzfeldt-Jakob disease.

    abstract:BACKGROUND:In definite Creutzfeldt-Jakob disease (CJD), morphological and immunohistochemical patterns are useful to identify molecular subtypes. Severe cerebellar pathology and hippocampal involvement helps to identify VV subtypes. The rare VV1 variant (<1%), more frequent in young individuals, is additionally charact...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1111/j.1365-2990.2011.01208.x

    authors: Martinez-Saez E,Gelpi E,Rey MJ,Ferrer I,Ribalta T,Botta-Orfila T,Nos C,Yagüe J,Sanchez-Valle R

    更新日期:2012-04-01 00:00:00

  • Sequential studies of a childhood myopathy: a clinical, histochemical and morphometric investigation.

    abstract::An unusual inherited progressive distal myopathy of early childhood onset is described in two sisters from a consanguineous Asian family. Motor milestones were normal but gait deteriorated slowly thereafter with development of generalized hypotonia and muscle weakness particularly in the wrist extensors and hand muscl...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1111/j.1365-2990.1989.tb01145.x

    authors: Mahon M,Kristmundsdottir F,Cumming WJ,Noronha MJ

    更新日期:1989-01-01 00:00:00

  • Low intensity ultrasound inhibits brain oedema formation in rats: potential action on AQP4 membrane localization.

    abstract:AIMS:Brain oedema is a major contributing factor to the morbidity and mortality of a variety of brain disorders. Although there has been considerable progress in our understanding of pathophysiological and molecular mechanisms associated with brain oedema so far, more effective treatment is required and is still awaite...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1111/nan.12182

    authors: Karmacharya MB,Kim KH,Kim SY,Chung J,Min BH,Park SR,Choi BH

    更新日期:2015-06-01 00:00:00

  • Review: Role of developmental inflammation and blood-brain barrier dysfunction in neurodevelopmental and neurodegenerative diseases.

    abstract::The causes of most neurological disorders are not fully understood. Inflammation and blood-brain barrier dysfunction appear to play major roles in the pathology of these diseases. Inflammatory insults that occur during brain development may have widespread effects later in life for a spectrum of neurological disorders...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1365-2990.2008.01005.x

    authors: Stolp HB,Dziegielewska KM

    更新日期:2009-04-01 00:00:00

  • Neuropil threads occur in dendrites of tangle-bearing nerve cells.

    abstract::Transparent Golgi preparations counterstained for Alzheimer's neurofibrillary changes rendered possible the demonstration of neuropil threads in defined cellular processes. Only dendrites of tangle-bearing cortical nerve cells were found to contain neuropil threads. Processes of glial cells as well as axons present in...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1111/j.1365-2990.1988.tb00864.x

    authors: Braak H,Braak E

    更新日期:1988-01-01 00:00:00

  • Loss of neurofibromatosis 1 (NF1) gene expression in NF1-associated pilocytic astrocytomas.

    abstract::The critical role of the neurofibromatosis 1 (NF1) gene as a tumour suppressor has been clearly demonstrated for malignancies arising in NF1 patients. However, little is known about the more common benign tumours, such as the pilocytic astrocytoma. Most NF1-associated astrocytomas are benign and clinically non-progres...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1046/j.1365-2990.2000.00258.x

    authors: Gutmann DH,Donahoe J,Brown T,James CD,Perry A

    更新日期:2000-08-01 00:00:00

  • Telomeric alterations in the default mode network during the progression of Alzheimer's disease: Selective vulnerability of the precuneus.

    abstract:AIMS:Although telomere length (TL) and telomere maintenance proteins (shelterins) are markers of cellular senescence and peripheral blood biomarkers of Alzheimer's disease (AD), little information is available on telomeric alterations during the prodromal stage (MCI) of AD. We investigated TL in the default mode networ...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1111/nan.12672

    authors: Mahady LJ,He B,Malek-Ahmadi M,Mufson EJ

    更新日期:2020-10-26 00:00:00

  • Oligodendrocyte progenitors in the embryonic spinal cord express DM-20.

    abstract::Oligodendrocyte progenitors, originating in the ventral ventricular zone of the embryonic rodent spinal cord, migrate and differentiate into the oligodendrocytes myelinating the future white matter. Transcripts for the dm-20 isoform of the proteolipid protein (plp) gene are detectable initially in cells of the ventral...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:

    authors: Dickinson PJ,Fanarraga ML,Griffiths IR,Barrie JM,Kyriakides E,Montague P

    更新日期:1996-06-01 00:00:00

  • Lysosomal storage results in impaired survival but normal neurite outgrowth in dorsal root ganglion neurones from a mouse model of Sandhoff disease.

    abstract::Sandhoff disease is a heritable lysosomal storage disease resulting from impaired degradation of GM2 ganglioside and related substrates. A mouse model of Sandhoff disease created by gene targeting displays progressive neurological manifestations, similar to patients with the disease. In the present in vivo and in vitr...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1046/j.1365-2990.2002.00366.x

    authors: Sango K,Yamanaka S,Ajiki K,Tokashiki A,Watabe K

    更新日期:2002-02-01 00:00:00

  • Review: Neuroinflammatory pathways as treatment targets and biomarker candidates in epilepsy: emerging evidence from preclinical and clinical studies.

    abstract::Accumulating evidence indicates an important pathophysiological role of brain inflammation in epilepsy. In this review, we will provide an update of specific inflammatory pathways that have been proposed to be crucial in the underlying molecular mechanisms of epilepsy, including the interleukin-1 receptor/toll-like re...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章,评审

    doi:10.1111/nan.12444

    authors: van Vliet EA,Aronica E,Vezzani A,Ravizza T

    更新日期:2018-02-01 00:00:00

  • Characterization of the microglial response in murine scrapie.

    abstract::The nature of the glial and inflammatory cell responses to infection in scrapie-affected brains was studied in terminally-affected mice of five scrapie models. There were marked astrocytic and microglial responses. Microglia showed increased staining of the surface antigens F4/80, leucocyte-common antigen, type 3 comp...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1111/j.1365-2990.1994.tb00956.x

    authors: Williams AE,Lawson LJ,Perry VH,Fraser H

    更新日期:1994-02-01 00:00:00

  • Amyloid beta peptide causes chronic glial cell activation and neuro-degeneration after intravitreal injection.

    abstract::We have previously demonstrated that amyloid beta (Abeta) peptide is acutely toxic to retinal neurones in vivo and that this toxicity is mediated by an indirect mechanism. We have now extended these studies to look at the chronic effect of intravitreal injection of Abeta peptides on retinal ganglion cells (RGC), the p...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1111/j.1365-2990.2005.00666.x

    authors: Walsh DT,Bresciani L,Saunders D,Manca MF,Jen A,Gentleman SM,Jen LS

    更新日期:2005-10-01 00:00:00

  • STAT3 represents a molecular switch possibly inducing astroglial instead of oligodendroglial differentiation of oligodendroglial progenitor cells in Theiler's murine encephalomyelitis.

    abstract:AIMS:Insufficient oligodendroglial differentiation of oligodendroglial progenitor cells (OPCs) is suggested to be responsible for remyelination failure and astroglial scar formation in Theiler's murine encephalomyelitis (TME). The aim of the present study is to identify molecular key regulators of OPC differentiation i...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1111/nan.12133

    authors: Sun Y,Lehmbecker A,Kalkuhl A,Deschl U,Sun W,Rohn K,Tzvetanova ID,Nave KA,Baumgärtner W,Ulrich R

    更新日期:2015-04-01 00:00:00

  • Neuronal apoptosis in HIV infection in adults.

    abstract::Productive infection of the central nervous system by HIV predominantly involves the white matter and basal ganglia. Involvement of the cerebral cortex with neuronal loss is also described in AIDS patients but not in asymptomatic HIV-positive patients. The mechanism of neuronal damage is unknown. To enquire whether ne...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1111/j.1365-2990.1995.tb01053.x

    authors: Adle-Biassette H,Levy Y,Colombel M,Poron F,Natchev S,Keohane C,Gray F

    更新日期:1995-06-01 00:00:00

  • Ubiquitin and heat shock protein expression in amyotrophic lateral sclerosis.

    abstract::The expression of two heat shock proteins, HSP72 and p57, in addition to ubiquitin, has been studied immunocytochemically in nine amyotrophic lateral sclerosis (ALS) cases and 10 age-matched controls. HSP72 and p57 antibodies did not identify the characteristic ubiquitin-immunoreactive inclusions present in anterior h...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1111/j.1365-2990.1991.tb00692.x

    authors: Garofalo O,Kennedy PG,Swash M,Martin JE,Luthert P,Anderton BH,Leigh PN

    更新日期:1991-02-01 00:00:00

  • Multifocal multinucleated giant cell myelitis in an AIDS patient.

    abstract::A 19-year-old male intravenous drug abuser, was admitted to hospital with a one-week history of lower limb weakness and urinary retention. He was known to have been HIV-seropositive for 3 years and had been treated for cerebral toxoplasmosis. Neurological examination confirmed flaccid paraparesis with weak ankle jerks...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1111/j.1365-2990.1991.tb00707.x

    authors: Geny C,Gherardi R,Boudes P,Lionnet F,Cesaro P,Gray F

    更新日期:1991-04-01 00:00:00

  • A neuronal DNA damage response is detected at the earliest stages of Alzheimer's neuropathology and correlates with cognitive impairment in the Medical Research Council's Cognitive Function and Ageing Study ageing brain cohort.

    abstract:AIMS:Population-based studies have shown that approximately 20% of the ageing population (aged 65 years and over) with dementia have little or no classical Alzheimer-type neuropathology. Cumulative DNA damage and a reduced capacity of DNA repair may result in neuronal dysfunction and contribute to cognitive impairment ...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1111/nan.12202

    authors: Simpson JE,Ince PG,Matthews FE,Shaw PJ,Heath PR,Brayne C,Garwood C,Higginbottom A,Wharton SB,MRC Cognitive Function and Ageing Neuropathology Study Group.

    更新日期:2015-06-01 00:00:00

  • Cryopreservation of viable human glioblastoma xenografts.

    abstract::Human tumour xenografts maintained in nude mice are a valuable research tool. The passaging and maintenance of human tumour xenografts in immune-deficient animals are expensive and labour-intensive. This study presents a protocol that permits long-term cryopreservation of viable glioblastoma xenograft tissue pieces in...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1046/j.1365-2990.2000.026002172.x

    authors: Goike HM,Asplund AC,Pettersson EH,Liu L,Ichimura K,Collins VP

    更新日期:2000-04-01 00:00:00

  • Adaptation of tibial nerve myelinated fibre parameters to reduced limb length caused by irradiation.

    abstract::Irradiation of a rat hind limb at 15 days of age caused marked shortening of the limb, with a consequent reduction in nerve length. The tibial nerves of the irradiated limbs were examined qualitatively and quantitatively, and compared with the unirradiated nerve. There was no evidence of fibre degeneration and only ve...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1111/j.1365-2990.1993.tb00404.x

    authors: Jacobs JM,Myers R

    更新日期:1993-02-01 00:00:00

  • Protein regulation of induced pluripotent stem cells by transplanting in a Huntington's animal model.

    abstract:AIMS:The purpose of this study was to determine the functional recovery and protein regulation by transplanted induced pluripotent stem cells in a rat model of Huntington's disease (HD). METHODS:In a quinolinic acid-induced rat model of striatal degeneration, induced pluripotent stem cells were transplanted into the i...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1111/nan.12315

    authors: Mu S,Han L,Zhou G,Mo C,Duan J,He Z,Wang Z,Ren L,Zhang J

    更新日期:2016-10-01 00:00:00

  • Absence of neuronal nitric oxide synthase (nNOS) as a pathological marker for the diagnosis of Becker muscular dystrophy with rod domain deletions.

    abstract::Immunohistochemistry using antibodies to dystrophin is the pathological basis for the diagnosis of Duchenne and Becker muscular dystrophy (DMD and BMD). While the sarcolemma of DMD muscle is negative, BMD muscle generally shows variable labelling because of the translation of a partially functional dystrophin that is ...

    journal_title:Neuropathology and applied neurobiology

    pub_type: 杂志文章

    doi:10.1111/j.1365-2990.2004.00561.x

    authors: Torelli S,Brown SC,Jimenez-Mallebrera C,Feng L,Muntoni F,Sewry CA

    更新日期:2004-10-01 00:00:00