Literature DB >> 6192875

The long term culture of bulk-isolated bovine oligodendroglia from adult brain.

W T Norton, M Farooq, K L Fields, C S Raine.   

Abstract

Oligodendroglia isolated from adult bovine brain by the method of Farooq et al. could be plated on polylysine-coated plastic dishes with an efficiency of 55-80%, and maintained in culture for as long as 4 months. The addition of cytosine arabinoside to the nutrient medium resulted in cultures that were approximately 90% oligodendroglia and 10% large fibroblasts. From 50 g of white matter 100-160 X 10(6) oligodendroglia, containing approximately 6-10 mg protein, could be obtained in culture. These small round cells started to send out processes at 5 days in vitro and by 2 weeks they formed an extensive network of processes. By immunofluorescence, all cells of this morphology were positive for galactocerebroside (GC) and myelin basic protein (MBP), and negative for glial filament protein and fibronectin. Most of the large flat cells were positive for fibronectin and negative for GC, MBP and glial filament protein. As the cultures aged the oligodendroglia tended to clump and blebs formed on the surface of both perikarya and processes. By 4 months they showed evidence of degeneration and detached from the substrate. Electron microscope examination showed that the cells had the appearance typical of oligodendroglia in situ. The somata were round to elliptical, with eccentrically placed nuclei, and were larger than freshly isolated cells. They grew directly on the substrate or on the surface of the fibroblasts. In older cultures the cells formed tight nests. The somata were enveloped by sheets of oligodendrocyte cytoplasm, sometimes having a myelin-like appearance. Gap junctions and small desmosomes were seen between oligodendroglial processes and between oligodendroglia and fibroblasts. The cytoplasm was characterized by a prominent Golgi apparatus, many mitochondria and lysosomes, scattered rough endoplasmic reticulum, free ribosomes, frequent centrioles and an abundance of microtubules. In cells from older cultures large vacuoles were common, and rarely they had multilamellar walls with alternating major and minor dense lines resembling myelin.

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Year:  1983        PMID: 6192875     DOI: 10.1016/0006-8993(83)90604-2

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  7 in total

1.  Tau protein expression in adult bovine oligodendrocytes: functional and pathological significance.

Authors:  Hanna Ksiezak-Reding; Muhammad Farooq; Liang-sheng Yang; Dennis W Dickson; Patrizia LoPresti
Journal:  Neurochem Res       Date:  2003-09       Impact factor: 3.996

2.  Expression of fibronectin and laminin by different types of mouse glial cells cultured in a serum-free medium.

Authors:  T Yoshida; M Takeuchi
Journal:  Cytotechnology       Date:  1991-11       Impact factor: 2.058

Review 3.  Do oligodendrocytes divide?

Authors:  W T Norton
Journal:  Neurochem Res       Date:  1996-04       Impact factor: 3.996

4.  Oligodendrocyte-specific autoreactive T cells using an alpha/beta T-cell receptor kill their target without self restriction.

Authors:  V Jewtoukoff; R Lebar; M A Bach
Journal:  Proc Natl Acad Sci U S A       Date:  1989-04       Impact factor: 11.205

5.  Growth requirements in vitro of oligodendrocyte cell lines and neonatal rat brain oligodendrocytes.

Authors:  J E Bottenstein
Journal:  Proc Natl Acad Sci U S A       Date:  1986-03       Impact factor: 11.205

6.  Isolation and cultivation of mature oligodendroglial cells.

Authors:  H H Althaus; H Montz; V Neuhoff; P Schwartz
Journal:  Naturwissenschaften       Date:  1984-06

7.  Emergence of three myelin proteins in oligodendrocytes cultured without neurons.

Authors:  M Dubois-Dalcq; T Behar; L Hudson; R A Lazzarini
Journal:  J Cell Biol       Date:  1986-02       Impact factor: 10.539

  7 in total

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