1997Humana Press eBooksRequires access

Generation of Oligodendroblasts from Primary Cultures of Rat Neopallium

B. H. J. Juurlink, Shawn K. Thorburne, Richard M. Devon

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Abstract

Several distinct stages of differentiation have been described for the oligodendroglial lineage in vitro (Gard and Pfeiffer, 1990; Gard et al., 1995). These include the actively proliferating bipolar or tripolar oligodendroglial precursor cell, characterized by the presence of GQ1c and GD3 gangliosides in the plasmalemma. The oligodendroglial precursor cell differentiates into the multipolar oligodendroblast, a proliferative cell that has sulfatide but no galactocerebroside in its plasmalemma. The oligodendroblast differentiates into the mitotically quiescent oligodendrocyte, a cell characterized by the presence of galactocerebroside in its plasmalemma. These oligodendrocytes also express other myelin-associated proteins, such as myelin basic protein. When transplanted into the central nervous system (CNS) of hypomyelinating hosts, oligodendrocyte precursors migrate over considerable distances and give rise to large numbers of myelinating oligodendrocytes; oligodendroblasts migrate only short distances and give rise to far fewer myelinating oligodendrocytes (Warrington et al., 1993). When transplanted into the CNS, the mature oligodendrocyte will also myelinate axons (Duncan et al., 1992).

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What this paper is about

Several distinct stages of differentiation have been described for the oligodendroglial lineage in vitro (Gard and Pfeiffer, 1990; Gard et al., 1995). These include the actively proliferating bipolar or tripolar oligodendroglial precursor cell, characterized by the presence of GQ1c and GD3 gangliosides in the plasmalemma. The oligodendroglial precursor cell differentiates into the multipolar oligodendroblast, a proliferative cell that has sulfatide but no galactocerebroside in its plasmalemma. The oligodendroblast differentiates into the mitotically quiescent oligodendrocyte, a cell characterized by the presence of galactocerebroside in its plasmalemma. These oligodendrocytes also express other myelin-associated proteins, such as myelin basic protein. When transplanted into the central nervous system (CNS) of hypomyelinating hosts, oligodendrocyte precursors migrate over considerable distances and give rise to large numbers of myelinating oligodendrocytes; oligodendroblasts migrate only short distances and give rise to far fewer myelinating oligodendrocytes (Warrington et al., 1993). When transplanted into the CNS, the mature oligodendrocyte will also myelinate axons (Duncan et al., 1992).

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Available abstract

Several distinct stages of differentiation have been described for the oligodendroglial lineage in vitro (Gard and Pfeiffer, 1990; Gard et al., 1995). These include the actively proliferating bipolar or tripolar oligodendroglial precursor cell, characterized by the presence of GQ1c and GD3 gangliosides in the plasmalemma. The oligodendroglial precursor cell differentiates into the multipolar oligodendroblast, a proliferative cell that has sulfatide but no galactocerebroside in its plasmalemma. The oligodendroblast differentiates into the mitotically quiescent oligodendrocyte, a cell characterized by the presence of galactocerebroside in its plasmalemma. These oligodendrocytes also express other myelin-associated proteins, such as myelin basic protein. When transplanted into the central nervous system (CNS) of hypomyelinating hosts, oligodendrocyte precursors migrate over considerable distances and give rise to large numbers of myelinating oligodendrocytes; oligodendroblasts migrate only short distances and give rise to far fewer myelinating oligodendrocytes (Warrington et al., 1993). When transplanted into the CNS, the mature oligodendrocyte will also myelinate axons (Duncan et al., 1992).

Key concepts: Galactocerebroside, Oligodendrocyte, Myelin, Biology, Myelin basic protein, Central nervous system, Cell biology, Precursor cell

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