Literature DB >> 6978754

Development of nodal and paranodal membrane specializations in amphibian peripheral nerves.

J H Tao-Cheng, J Rosenbluth.   

Abstract

Peripheral nerves from the hind legs of frog tadpoles were examined in order to ascertain the pattern of development of nodal and paranodal specializations in myelinated fibers. In thin sections the earliest detectable node-related specializations resemble "intermediate" junctions between axons and Schwann cell processes. These occur in individually ensheathed axons near the edges of the sheath segments and could represent early nodal or paranodal components or transient structures. The characteristic nodal "undercoating" is indistinct and highly variable in thickness in immature fibers and its density is lower in developing nodes than in adult nodes. Corresponding freeze-fracture replicas of developing axons demonstrate aggregates of nodal E face particles whose concentration is lower than that in the adult. Such aggregates usually occur immediately adjacent to Schwann cell indentations, even though early in development the latter may not exhibit the paracrystalline pattern seen in the adult paranodal axolemma. On rare occasions, node-like particle aggregates and presumptive nodal undercoatings have been observed without recognizable paranodal junctions or indentations nearby. However, neither specialization has been found in axons not individually ensheathed by Schwann cells. Paranodal Schwann cell loops are widely separated and irregularly arranged in the developing nodes, and the paranodal regions flanking a node usually mature asymmetrically. Differentiated paranodal junctions appear early in axons ensheathed by only a few loose Schwann cell lamellae. However, such junctions are not formed by all paranodal loops; they consistently appear first in the loops close to the node and only later in those further removed. No junctional specialization has been observed in either the axolemma or the Schwann cell membrane without the close association of the other.

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Year:  1982        PMID: 6978754     DOI: 10.1016/0165-3806(82)90055-4

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  7 in total

1.  Nodes of Ranvier form in association with ezrin-radixin-moesin (ERM)-positive Schwann cell processes.

Authors:  C V Melendez-Vasquez; J C Rios; G Zanazzi; S Lambert; A Bretscher; J L Salzer
Journal:  Proc Natl Acad Sci U S A       Date:  2001-01-30       Impact factor: 11.205

2.  Paranodal reorganization results in the depletion of transverse bands in the aged central nervous system.

Authors:  Mark N Shepherd; Anthony D Pomicter; Cristine S Velazco; Scott C Henderson; Jeffrey L Dupree
Journal:  Neurobiol Aging       Date:  2010-10-02       Impact factor: 4.673

3.  Dynamic potassium channel distributions during axonal development prevent aberrant firing patterns.

Authors:  I Vabnick; J S Trimmer; T L Schwarz; S R Levinson; D Risal; P Shrager
Journal:  J Neurosci       Date:  1999-01-15       Impact factor: 6.167

4.  Developmental changes at the node and paranode in human sural nerves: morphometric and fine-structural evaluation.

Authors:  M Bertram; J M Schröder
Journal:  Cell Tissue Res       Date:  1993-09       Impact factor: 5.249

Review 5.  Electrophysiology and morphology of myelinated nerve fibers. V. Intramembranous particle distribution in nerve fiber membranes.

Authors:  J Rosenbluth
Journal:  Experientia       Date:  1983-09-15

Review 6.  Molecular constituents of the node of Ranvier.

Authors:  Katie Kazarinova-Noyes; Peter Shrager
Journal:  Mol Neurobiol       Date:  2002 Oct-Dec       Impact factor: 5.682

7.  The axonal membrane protein Caspr, a homologue of neurexin IV, is a component of the septate-like paranodal junctions that assemble during myelination.

Authors:  S Einheber; G Zanazzi; W Ching; S Scherer; T A Milner; E Peles; J L Salzer
Journal:  J Cell Biol       Date:  1997-12-15       Impact factor: 10.539

  7 in total

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