๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Mitotic potential of adult rat oligodendrocytes in culture

โœ Scribed by R. S. Vick; Dr. G. H. DeVries


Publisher
John Wiley and Sons
Year
1992
Tongue
English
Weight
708 KB
Volume
33
Category
Article
ISSN
0360-4012

No coin nor oath required. For personal study only.

โœฆ Synopsis


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 pulse of 3H thymidine during the first 4 days of co-culture. From day 4 to day 6 there was a dramatic increase in proliferation which reached a plateau at 40% and gradually decreased to 25% from days 10 to 20 of co-culture. Axolemma-enriched fractions (AEF) were weak mitogens for OLGs (less than 5% proliferation after 7 days of stimulation), however, heparin extracts of AEF were five-fold more mitogenic than the AEF from which they were derived. Basic and acidic fibroblast growth factor were effective mitogens for the adult OLGs (labelling indices of 28% and 12%, respectively) provided that the cells were treated for 7 days with the growth factor and that the cells had been in culture for at least 14 days. Other soluble growth factors (IL-2 and PDGF) gave no mitotic response. We conclude that adult OLGs are mitotically responsive to mitogens provided that (1) the adult OLG has been cultured for sufficient time (I4 days, acidic or basic fibroblast growth factor); (2) the axonal mitogen is allowed to interact with the OLG for a sufficient time (neuritic mitogen); and (3) the axonal mitogen is presented to the OLG in an activated form (AEF-heparin extract).


๐Ÿ“œ SIMILAR VOLUMES


Isolation, culture, and characterization
โœ R. S. Vick; S.-J. Chen; G. H. DeVries ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 944 KB

Investigation into CNS demyelinating diseases, which usually occur in adults, can be facilitated by the use of a good in vitro model. We have established a methodology whereby oligodendrocytes from adult rat CNS can be cultured in vitro, and we have characterized these cultures morphologically and i

Regenerative potential of adult O1+ olig
โœ Caterina Rosano; Ernesto Felipe-Cuervo; Patrick M. Wood ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 920 KB

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 320:7

Single channel potassium currents in cul
โœ Dr. James G. McLarnon; Seung U. Kim ๐Ÿ“‚ Article ๐Ÿ“… 1989 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 973 KB

These studies have enabled the first characterization of the properties of ion channels in adult oligodendrocytes. Cell-attached recordings from cultured adult bovine cells showed channel activity with 140 mM KC1 in the patch pipette; the amplitude of the currents was increased with increasing membr

Cell cycle and proliferation dynamics of
โœ R. S. Vick; J. M. Collins; Dr. G. H. Devries ๐Ÿ“‚ Article ๐Ÿ“… 1992 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 597 KB

Adult oligodendrocytes (OLGs) have been shown to be mitotically responsive when co-cultured with dorsal root ganglion. We have investigated the population dynamics of the OLG proliferative response, including the maximum percent of cells which will proliferate and the cell cycle duration time of the