Increased numbers of oligodendrocyte lineage cells in the optic nerves of cerebroside sulfotransferase knockout mice

Sulfatide is a myelin glycolipid that functions in the formation of paranodal axo-glial junctions in vivo and in the regulation of oligodendrocyte differentiation in vitro. Cerebroside sulfotransferase (CST) catalyzes the production of two sulfated glycolipids, sulfatide and proligodendroblast antigen, in oligodendrocyte lineage cells. Recent studies have demonstrated significant increases in oligodendrocytes from the myelination stage through adulthood in brain and spinal cord under CST-deficient conditions. However, whether these result from excess migration or in situ proliferation during development is undetermined. In the present study, CST-deficient optic nerves were used to examine migration and proliferation of oligodendrocyte precursor cells (OPCs) under sulfated glycolipid-deficient conditions. In adults, more NG2-positive OPCs and fully differentiated cells were observed. In developing optic nerves, the number of cells at the leading edge of migration was similar in CST-deficient and wild-type mice. However, BrdU+ proliferating OPCs were more abundant in CST-deficient mice. These results suggest that sulfated glycolipids may be involved in proliferation of OPCs in vivo

Purification and analysis of in vivo-differentiated oligodendrocytes expressing the green fluorescent protein

A complete understanding of the molecular mechanisms involved in the formation and repair of the central nervous system myelin sheath requires an unambiguous identification and isolation of in vivo-differentiated myelin- forming cells. In order to develop a novel tool for the analysis of in vivo- differentiated oligodendrocytes, we generated transgenic mice expressing a red-shifted variant of the green fluorescent protein under the control of the proteolipid protein promoter. We demonstrate here that green fluorescent protein-derived fluorescence in the central nervous system of 9-day- to 7- week-old mice is restricted to mature oligodendrocytes, as determined by its spatiotemporal appearance and by both immunocytochemical and electrophysiological criteria. Green fluorescent protein-positive oligodendrocytes could easily be visualized in live and fixed tissue. Furthermore, we show that this convenient and reliable identification now allows detailed physiological analyses of differentiated oligodendrocytes in situ. In addition, we developed a novel tissue culture system for in vivo- differentiated oligodendrocytes. Initial data using this system indicate that, for oligodendrocytes isolated after differentiation in vivo, as yet unidentified factors secreted by astrocytes are necessary for survival and/or reappearance of a mature phenotype in culture

Lichenometric dating: a commentary, in the light of some recent statistical studies

This commentary article discusses the relative merits of new mathematical approaches to lichenometry. It highlights their strong reliance on complex statistics; their user un-friendliness; and their occasional mistreatment of existing lichenometric techniques. The article proposes that the success of lichenometric dating over the past 50 years has stemmed from its relative simplicity, transparency, and general field applicability. It concludes that any new techniques which ignore these principles are likely to be unjustified, unsuitable to the user community and inappropriate for the subject matter. Furthermore, the article raises a more general philosophical question: can statistical complexity and high precision in a ‘geobotanical’ dating technique, fraught with high degrees of environmental variability and in-built uncertainty, ever be scientifically valid

Use of Bomb-14C to investigate the growth and carbon turnover rates of a crustose lichen

The reliability of lichenometric dating is dependent on a good understanding of lichen growth rates. The growth rate of lichens can be determined from direct measurement of growing lichens or indirect methods by measuring lichens growing on surfaces of known age, although there are limitations to both approaches. Radiocarbon (14C) analysis has previously been used in only a handful of studies to determine lichen growth rates of two species from a small area of North America. These studies have produced mixed results; a small amount of carbon turnover appears to occur in one of the species (Caloplaca spp.) previously investigated introducing uncertainty in the growth rate, while much higher carbon cycling occurred in another (Rhizocarpon geographicum), making the 14C approach unsuitable for estimating growth rates in the species most commonly used in lichenometric dating. We investigated the use of bomb-14C analysis to determine the growth rate of a different crustose species (Pertusaria pseudocorallina) common to Northern Europe. 14C-based growth rates were considerably higher than growth rates of morphologically similar species based on direct measurement made at locations nearby and elsewhere in the UK. This observation strongly suggests that a degree of carbon turnover probably occurs in Pertusaria pseudocorallina, and that bomb-14C analysis alone cannot be used to determine lichen age or absolute growth rates in this lichen species