scholarly journals Neuronal cell adhesion molecules and cytotactin are colocalized at the node of Ranvier.

1986 ◽  
Vol 103 (2) ◽  
pp. 379-391 ◽  
Author(s):  
F Rieger ◽  
J K Daniloff ◽  
M Pincon-Raymond ◽  
K L Crossin ◽  
M Grumet ◽  
...  

Immunocytochemical methods were used to show that Ng-CAM (the neuron-glia cell adhesion molecule), N-CAM (the neural cell adhesion molecule), and the extracellular matrix protein cytotactin are highly concentrated at nodes of Ranvier of the adult chicken and mouse. In contrast, unmyelinated axonal fibers were uniformly stained by specific antibodies to both CAMs but not by antibodies to cytotactin. Ultrastructural immunogold techniques indicated that both N-CAM and Ng-CAM were enriched in the nodal axoplasm and axolemma of myelinated fibers as well as within the nodal regions of the myelinating Schwann cell. At embryonic day 14, before myelination had occurred, small-caliber fibers of chick embryos showed periodic coincident accumulations of the two CAMs but not of cytotactin, with faint labeling in the axonal regions between accumulations. Cytotactin was found on Schwann cells and in connective tissue. By embryonic day 18, nodal accumulations of CAMs were first observed in a few medium- and large-caliber fibers. Immunoblot analyses indicated that embryonic to adult conversion of N-CAM and a progressive decrease in the amount of Ng-CAM and N-CAM occurred while nodes were forming. Sciatic nerves of mouse mutants with defects in cell interactions showed abnormalities in the distribution patterns and amount of Ng-CAM, N-CAM, and cytotactin that were consistent with the known morphological nodal disorders. In trembler (+/Tr), intense staining for both CAMs appeared all along the fibers and the amounts of N-CAM in the sciatic nerve were found to be increased. In mice with motor endplate disease (med/med), Ng-CAM and N-CAM, but not cytotactin, were localized in the widened nodes. Both trembler and med/med Schwann cells stained intensely for cytotactin, in contrast to normal Schwann cells which stained only slightly. All of these findings are consistent with the hypothesis that surface modulation of neuronal CAMs mediated by signals shared between neurons and glia may be necessary for establishing and maintaining the nodes of Ranvier.

2001 ◽  
Vol 154 (2) ◽  
pp. 427-434 ◽  
Author(s):  
Charlotte F. Ratcliffe ◽  
Ruth E. Westenbroek ◽  
Rory Curtis ◽  
William A. Catterall

Sequence homology predicts that the extracellular domain of the sodium channel β1 subunit forms an immunoglobulin (Ig) fold and functions as a cell adhesion molecule. We show here that β1 subunits associate with neurofascin, a neuronal cell adhesion molecule that plays a key role in the assembly of nodes of Ranvier. The first Ig-like domain and second fibronectin type III–like domain of neurofascin mediate the interaction with the extracellular Ig-like domain of β1, confirming the proposed function of this domain as a cell adhesion molecule. β1 subunits localize to nodes of Ranvier with neurofascin in sciatic nerve axons, and β1 and neurofascin are associated as early as postnatal day 5, during the period that nodes of Ranvier are forming. This association of β1 subunit extracellular domains with neurofascin in developing axons may facilitate recruitment and concentration of sodium channel complexes at nodes of Ranvier.


2008 ◽  
Vol 12 (01) ◽  
pp. 1 ◽  
Author(s):  
Tetsuya Marui ◽  
Ikuko Funatogawa ◽  
Shinko Koishi ◽  
Kenji Yamamoto ◽  
Hideo Matsumoto ◽  
...  

2000 ◽  
Vol 21 ◽  
pp. 133 ◽  
Author(s):  
Wim G. Annaert ◽  
Christine Boeve ◽  
Cary Esselens ◽  
Greet Snellings ◽  
Kathleen Craessaerts ◽  
...  

2004 ◽  
Vol 167 (5) ◽  
pp. 973-983 ◽  
Author(s):  
Satoshi Fukumoto ◽  
Takayoshi Kiba ◽  
Bradford Hall ◽  
Noriyuki Iehara ◽  
Takashi Nakamura ◽  
...  

Tooth morphogenesis results from reciprocal interactions between oral epithelium and ectomesenchyme culminating in the formation of mineralized tissues, enamel, and dentin. During this process, epithelial cells differentiate into enamel-secreting ameloblasts. Ameloblastin, an enamel matrix protein, is expressed by differentiating ameloblasts. Here, we report the creation of ameloblastin-null mice, which developed severe enamel hypoplasia. In mutant tooth, the dental epithelium differentiated into enamel-secreting ameloblasts, but the cells were detached from the matrix and subsequently lost cell polarity, resumed proliferation, and formed multicell layers. Expression of Msx2, p27, and p75 were deregulated in mutant ameloblasts, the phenotypes of which were reversed to undifferentiated epithelium. We found that recombinant ameloblastin adhered specifically to ameloblasts and inhibited cell proliferation. The mutant mice developed an odontogenic tumor of dental epithelium origin. Thus, ameloblastin is a cell adhesion molecule essential for amelogenesis, and it plays a role in maintaining the differentiation state of secretory stage ameloblasts by binding to ameloblasts and inhibiting proliferation.


2011 ◽  
Vol 29 (15_suppl) ◽  
pp. e21138-e21138
Author(s):  
J. Jassem ◽  
R. Duchnowska ◽  
W. Biernat ◽  
L. M. Evans ◽  
D. P. Fitzgerald ◽  
...  

2000 ◽  
Vol 275 (44) ◽  
pp. 34701-34709 ◽  
Author(s):  
Kohji Kasahara ◽  
Kazutada Watanabe ◽  
Kosei Takeuchi ◽  
Harumi Kaneko ◽  
Atsuhiko Oohira ◽  
...  

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