1998), while OLs from forebrain exhibit three different waves of OL progenitors that are generated from different origins (Kessaris et al. 2006; Richardson et al. 2006). In addition, the behaviors of competition for growth factors are also different in OL progenitors derived from the spinal cord versus the cerebral cortex (Bradl and Lassmann 2010). Therefore, it is quite possible that the intrinsic potential of differentiation Inhibitors,research,lifescience,medical in the spinal cord derived OLs is much greater than that from the cortex. Interestingly, our data also suggested that the cell phenotypes may also be different between these two CNS-derived

cultures, and they may also contribute to the disparity noted in OL maturation between these two cultures. Lastly, recent studies have suggested that neuronal/axonal factors (i.e., adhesion molecules expressed Inhibitors,research,lifescience,medical on axonal surface, electrical activity, size, etc.) may play important roles in controlling myelination (Piaton et al. 2010). The difference between neuronal phenotype, that is, predominantly sensory and motor neurons in the spinal cord versus a diversity of neurons in the cerebral cortex may also account for the difference

in myelination potential. Nevertheless, when OL progenitors Inhibitors,research,lifescience,medical were forced to mature by T3, successful myelination occurred in the cortex-derived culture, suggesting that the lack of OL maturation may be the major cause of myelination Inhibitors,research,lifescience,medical failure in the cortex-derived culture. Nodes of Ranvier are important structures of myelinated axons that ensure the propagation of rapid, saltatory nerve conduction. The nodes are comprised of several subdomains including the node, paranode, and selleck compound juxtaparanode regions that can be identified with specific markers (Southwood et al. 2004; Simons and Trajkovic 2006). Using paranodal marker Caspr and juxtaparanodal marker Inhibitors,research,lifescience,medical Kv1.2,

our data revealed that the typical nodes of Ranvier were successfully constructed. In addition to myelination, abundant synapses with a variety of specification were also found ultrastructurally, suggesting that unless our culture system recapitulates the developmental features similar to the in vivo environment. Another feature of our myelination culture system is that quantification of myelination can be conducted using both the manual counting and ImageJ approaches. The direct quantification of myelin segments (although we only measured the number, the length can also be determined) can provide additional information other than quantifying the amount of myelin proteins. For instance, early studies using in vitro myelination models, for example, the aggregate culture, measured the amount of myelin proteins (e.g., MBP) as an index for myelination (Diemel et al. 2004).