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      Primary Culture of Central Neurocytoma: A Case Report

      case-report

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          Abstract

          A seventeen-year-old female patient was admitted with sudden-onset of headache and vomiting. Brain magnetic resonance imaging demonstrated a heterogeneously enhancing tumour in the left lateral ventricle. The tumour was removed and confirmed as a central neurocytoma (CN). For the residual tumour in the left lateral ventricle, gamma knife stereotactic radiosurgery was done at fifteen months after the initial surgery. Tumour recurred in the 4th ventricle at 5 yr after initial surgery. The tumour was removed and proved as a CN. In vitro primary culture was done with both tumours obtained from the left lateral ventricle and the 4th ventricle, respectively. Nestin, a neuronal stem cell marker was expressed in reverse Transcriptase-Polymerase Chain Reaction of both tumors. Both tumours showed different morphology and phenotypes of neuron and glia depending on the culture condition. When cultured in insulin, transferrin selenium and fibronectin media with basic fibroblast growth factors, tumour cells showed neuronal morphology and phenotypes. When cultured in the Dulbeco's Modified Essential Media with 20% fetal bovine serum, tumors cells showed glial morphology and phenotypes. It is suggested that CN has the characteristics of neuronal stem cells and potential to differentiate into mature neuron and glial cells depending on the environmental cue.

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          Isolation of radial glial cells by fluorescent-activated cell sorting reveals a neuronal lineage.

          The developing central nervous system of vertebrates contains an abundant cell type designated radial glial cells. These cells are known as guiding cables for migrating neurons, while their role as precursor cells is less clear. Since radial glial cells express a variety of astroglial characteristics and differentiate as astrocytes after completing their guidance function, they have been considered as part of the glial lineage. Using fluorescence-activated cell sorting, we show here that radial glial cells also are neuronal precursors and only later, after neurogenesis, do they shift towards an exclusive generation of astrocytes. These results thus demonstrate a novel function for radial glial cells, namely their ability to generate two major cell types found in the nervous system, neurons and astrocytes.
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            A glial progenitor cell that develops in vitro into an astrocyte or an oligodendrocyte depending on culture medium.

            We have identified a cell type in 7-day-old rat optic nerve that differentiates into a fibrous astrocyte if cultured in the presence of fetal calf serum and into an oligodendrocyte if cultured in the absence of serum. In certain culture conditions some of these cells acquire a mixed phenotype, displaying properties of both astrocytes and oligodendrocytes. These observations suggest that fibrous astrocytes and oligodendrocytes develop from a common progenitor cell and provide a striking example of developmental plasticity and environmental influence in the differentiation of CNS glial cells.
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              Neurogenesis in the adult brain.

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                Author and article information

                Journal
                J Korean Med Sci
                JKMS
                Journal of Korean Medical Science
                The Korean Academy of Medical Sciences
                1011-8934
                1598-6357
                May 2010
                16 April 2010
                : 25
                : 5
                : 798-803
                Affiliations
                [1 ]Department of Neurosurgery, Seoul National University College of Medicine, Seoul National University, Seoul, Korea.
                [2 ]Department of Pathology, Seoul National University College of Medicine, Seoul National University, Seoul, Korea.
                [3 ]Laboratory of Neuroprotection, Division of Life Pharmaceutical Sciences, Brain Disease Rescarch Institute, College of Pharmacy, Ewha Woman's University, Seoul, Korea.
                Author notes
                Address for correspondence: Dong Gyu Kim, M.D. Department of Neurosurgery, Seoul National University Hospital, 101 Daehang-no, Jongno-gu, Seoul, 110-744, Korea. Tel: +82.2-2072-2874, Fax: +82.2-744-8459, gknife@ 123456plaza.snu.ac.kr
                Article
                10.3346/jkms.2010.25.5.798
                2858845
                20436722
                53915123-a491-4a76-b22d-0e698b336a79
                © 2010 The Korean Academy of Medical Sciences.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 23 October 2008
                : 24 March 2009
                Categories
                Case Report
                Neuroscience

                Medicine
                neuronal stem cells,neurocytoma,cell culture techniques
                Medicine
                neuronal stem cells, neurocytoma, cell culture techniques

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