## Abstract In myelinated axons, voltageβgated sodium channels specifically cluster at the nodes of Ranvier, while voltageβgated potassium channels are located at the juxtaparanodes. These characteristic localizations are influenced by myelination. During development, Nav1.2 first appears in the pr
Signaling proteins in the axoglial apparatus of sciatic nerve nodes of Ranvier
β Scribed by Joanna C. Toews; Vincent Schram; Susanna H. Weerth; Gregory A. Mignery; James T. Russell
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 1021 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0894-1491
No coin nor oath required. For personal study only.
β¦ Synopsis
During action potential conduction, the axonal specializations at the node, together with the adjacent paranodal terminations of the myelin sheath, interact with glial processes that invest the nodal gap. The nature of the mutual signals between axons and myelinating glia, however, are not well understood. Here we have characterized the distribution of inositol 1,4,5-trisphosphate receptors (IP 3 Rs) in the axoglial apparatus by immunohistochemistry, using known myelin domain-specific markers. While IP 3 R1 is not expressed in the Schwann cells or the axon, IP 3 R2 and IP 3 R3 are expressed in distinct cellular domains, suggesting distinct signaling roles for the two receptors. IP 3 R3 is the most predominant isoform in Schwann cells, and is expressed in particularly dense patches in the paranodal region. In addition to IP 3 Rs, two other members of the metabotropic Ca 21 signaling pathway, G a q, and P 2 Y1 type of purinoceptors were also found in Schwann cells. Their pattern of expression matches the expression of their signaling partners, the IP 3 Rs. One interesting finding to emerge from this study is the expression of connexin 32 (Cx32) in close proximity with IP 3 R3. Although IP 3 R3 and Cx32 are not colocalized, their expression in the same membrane areas raises the question whether Schwann cell Ca 21 signals either control the function of the gap junctions, or whether the gap junctional channels serve as conduits for rapid radial spread of Ca 21 signals initiated during action potential propagation.
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