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Tight junctions in differentiating ameloblasts and odontoblasts differentially express ZO‐1, occludin, and claudin‐1 in early odontogenesis of rat molars
Little is known about the expression of associated proteins during the assembly of tight junctions (TJs). We studied the distribution of ZO‐1, occludin, and claudin‐1 between differentiating ameloblasts and odontoblasts in molar tooth germs from 1‐ to 3‐day‐old rats by confocal laser scanning micros...
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Published in: | The Anatomical record 2004-04, Vol.277A (2), p.338-343 |
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description | Little is known about the expression of associated proteins during the assembly of tight junctions (TJs). We studied the distribution of ZO‐1, occludin, and claudin‐1 between differentiating ameloblasts and odontoblasts in molar tooth germs from 1‐ to 3‐day‐old rats by confocal laser scanning microscopy. Immunoreactivity for ZO‐1 was strong at proximal and distal junctional complexes of differentiating ameloblasts, while it was weak and punctuate at the distal region of differentiating odontoblasts. Occludin was immunoreactive at distal and proximal complexes of early differentiating ameloblasts and at distal regions of differentiating odontoblasts. However, in more advanced stages, occludin was only evident at the proximal complex of ameloblasts. Claudin‐1 was strongly detected at the proximal complex but it was weak at distal complex of late differentiating ameloblasts. Thus, our results showed that ZO‐1, occludin, and claudin‐1 are differentially expressed as TJs assemble for regulating polarity and/or paracellular permeability in differentiating ameloblasts and odontoblasts. Anat Rec Part A 277A:338–343, 2004. © 2004 Wiley‐Liss, Inc. |
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We studied the distribution of ZO‐1, occludin, and claudin‐1 between differentiating ameloblasts and odontoblasts in molar tooth germs from 1‐ to 3‐day‐old rats by confocal laser scanning microscopy. Immunoreactivity for ZO‐1 was strong at proximal and distal junctional complexes of differentiating ameloblasts, while it was weak and punctuate at the distal region of differentiating odontoblasts. Occludin was immunoreactive at distal and proximal complexes of early differentiating ameloblasts and at distal regions of differentiating odontoblasts. However, in more advanced stages, occludin was only evident at the proximal complex of ameloblasts. Claudin‐1 was strongly detected at the proximal complex but it was weak at distal complex of late differentiating ameloblasts. Thus, our results showed that ZO‐1, occludin, and claudin‐1 are differentially expressed as TJs assemble for regulating polarity and/or paracellular permeability in differentiating ameloblasts and odontoblasts. 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We studied the distribution of ZO‐1, occludin, and claudin‐1 between differentiating ameloblasts and odontoblasts in molar tooth germs from 1‐ to 3‐day‐old rats by confocal laser scanning microscopy. Immunoreactivity for ZO‐1 was strong at proximal and distal junctional complexes of differentiating ameloblasts, while it was weak and punctuate at the distal region of differentiating odontoblasts. Occludin was immunoreactive at distal and proximal complexes of early differentiating ameloblasts and at distal regions of differentiating odontoblasts. However, in more advanced stages, occludin was only evident at the proximal complex of ameloblasts. Claudin‐1 was strongly detected at the proximal complex but it was weak at distal complex of late differentiating ameloblasts. Thus, our results showed that ZO‐1, occludin, and claudin‐1 are differentially expressed as TJs assemble for regulating polarity and/or paracellular permeability in differentiating ameloblasts and odontoblasts. 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We studied the distribution of ZO‐1, occludin, and claudin‐1 between differentiating ameloblasts and odontoblasts in molar tooth germs from 1‐ to 3‐day‐old rats by confocal laser scanning microscopy. Immunoreactivity for ZO‐1 was strong at proximal and distal junctional complexes of differentiating ameloblasts, while it was weak and punctuate at the distal region of differentiating odontoblasts. Occludin was immunoreactive at distal and proximal complexes of early differentiating ameloblasts and at distal regions of differentiating odontoblasts. However, in more advanced stages, occludin was only evident at the proximal complex of ameloblasts. Claudin‐1 was strongly detected at the proximal complex but it was weak at distal complex of late differentiating ameloblasts. Thus, our results showed that ZO‐1, occludin, and claudin‐1 are differentially expressed as TJs assemble for regulating polarity and/or paracellular permeability in differentiating ameloblasts and odontoblasts. 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subjects | ameloblasts Ameloblasts - cytology Ameloblasts - metabolism Animals Cell Differentiation - physiology Claudin-1 Maxilla Membrane Proteins - metabolism Molar - cytology Molar - growth & development Molar - metabolism Occludin odontoblasts Odontoblasts - cytology Odontoblasts - metabolism odontogenesis Odontogenesis - physiology Phosphoproteins - metabolism Rats Rats, Wistar tight junction Tight Junctions - metabolism Zonula Occludens-1 Protein ZO‐1 |
title | Tight junctions in differentiating ameloblasts and odontoblasts differentially express ZO‐1, occludin, and claudin‐1 in early odontogenesis of rat molars |
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