The proliferation of adult oligodendrocytes (OLGs) was examined in response to membrane bound and soluble mitogens. OLGs were isolated according to Vick, et al., J Neurosci Res 25524534, 1990, and co-cultured with dorsal root ganglia (DRGs). Less than 5 % of the total cells incorporated a 48 hr puls
Regenerative potential of adult O1+ oligodendrocytes
โ Scribed by Caterina Rosano; Ernesto Felipe-Cuervo; Patrick M. Wood
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 920 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0894-1491
No coin nor oath required. For personal study only.
โฆ Synopsis
Remyelination in the adult central nervous system (CNS) is preceded by the generation of new oligodendrocytes (ODCs) but the source of the new ODCs has not been resolved. Adult galactocerebroside positive (O1ฯฉ)ODCs proliferate when cultured with purified sensory neurons (Wood and Bunge, Nature 320:756-758, 1999), implying that differentiated ODCs could be an important source of new myelinating ODCs. To test this possibility purified O1ฯฉODCs (ฯพ96% purity) were plated at low density (20-50 cells/culture) into cultures of purified dorsal root ganglion neurons. Three days after plating, single O1ฯฉODCs were located (209 ODCs/43 cultures) and sequentially observed for 4 weeks. The ODCs began to proliferate by the fifth day after plating and formed large colonies by the third week. Most cells in these colonies were 01ฯช but positive for another ODC antigen, O4. A few O1ฯฉ, myelin basic protein (MBP)ฯฉODCs, and glial fibrillary acidic protein (GFAP)ฯฉcells with astrocytic morphology were observed in some colonies. In similar cultures plated with cell-sorted O1ฯฉODCs (ฯพ99.5% purity), ciliary neurotrophic factor (CNTF, 1ng/ml) increased the number and size of colonies, the number of O1ฯฉMBPฯฉODCs (including ODCs producing myelin-like profiles in association with axons) and the number of GFAPฯฉ astrocytes, relative to untreated controls. The results are evidence that CNTF exerts a trophic effect on adult O1ฯฉODCs, and/or their progeny, and that cells generated by division of O1ฯฉODCs can become either new myelinproducing ODC, or astrocytes. This plasticity in regenerative potential of adult O1ฯฉODCs has not been previously demonstrated.
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