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TGFβ-Smad signalling in postoperative human lens epithelial cells

Identifieur interne : 002640 ( Pmc/Checkpoint ); précédent : 002639; suivant : 002641

TGFβ-Smad signalling in postoperative human lens epithelial cells

Auteurs : S. Saika [Japon] ; T. Miyamoto [Japon] ; I. Ishida [Japon] ; K. Shirai [Japon] ; Y. Ohnishi [Japon] ; A. Ooshima [Japon] ; J W Mcavoy [Australie]

Source :

RBID : PMC:1771405

Abstract

Aims: To localise Smads3/4 proteins in lens epithelial cells (LECs) of fresh and postoperative human specimens. Smads3/4 are involved in signal transduction between transforming growth factor β (TGFβ) cell surface receptors and gene promoters. Nuclear localisation of Smads indicates achievement of endogenous TGFβ signalling in cells.

Methods: Three circular sections of the anterior capsule, one lens, and 17 capsules undergoing postoperative healing were studied. Immunohistochemistry was performed for Smads3/4 in paraffin sections of the specimens. The effect of exogenous TGFβ2 on Smad3 subcellular localisation was examined in explant cultures of extracted human anterior lens epithelium.

Results: The cytoplasm, but not the nuclei, of LECs of uninjured lenses was immunoreactive for Smads3/4. In contrast, nuclear immunoreactivity for Smads3/4 was detected in LECs during capsular healing. Nuclei positive for Smads3/4 were observed in monolayered LECs adjacent to the regenerated lens fibres of Sommerring’s ring. Interestingly, the nuclei of LECs that were somewhat elongated, and appeared to be differentiating into fibre-like cells, were negative for Smads3/4. Fibroblast-like, spindle-shaped lens cells with nuclear immunoreactivity for nuclear Smads3/4 were occasionally observed in the extracellular matrix accumulated in capsular opacification. Exogenous TGFβ induced nuclear translocation of Smad3 in LECs of anterior capsule specimens in explant culture.

Conclusions: This is consistent with TGFβ induced Smad signalling being involved in regulating the behaviour of LECs during wound healing after cataract surgery.


Url:
PubMed: 12446380
PubMed Central: 1771405


Affiliations:


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PMC:1771405

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<bold>Aims:</bold>
To localise Smads3/4 proteins in lens epithelial cells (LECs) of fresh and postoperative human specimens. Smads3/4 are involved in signal transduction between transforming growth factor β (TGFβ) cell surface receptors and gene promoters. Nuclear localisation of Smads indicates achievement of endogenous TGFβ signalling in cells.</p>
<p>
<bold>Methods:</bold>
Three circular sections of the anterior capsule, one lens, and 17 capsules undergoing postoperative healing were studied. Immunohistochemistry was performed for Smads3/4 in paraffin sections of the specimens. The effect of exogenous TGFβ2 on Smad3 subcellular localisation was examined in explant cultures of extracted human anterior lens epithelium.</p>
<p>
<bold>Results:</bold>
The cytoplasm, but not the nuclei, of LECs of uninjured lenses was immunoreactive for Smads3/4. In contrast, nuclear immunoreactivity for Smads3/4 was detected in LECs during capsular healing. Nuclei positive for Smads3/4 were observed in monolayered LECs adjacent to the regenerated lens fibres of Sommerring’s ring. Interestingly, the nuclei of LECs that were somewhat elongated, and appeared to be differentiating into fibre-like cells, were negative for Smads3/4. Fibroblast-like, spindle-shaped lens cells with nuclear immunoreactivity for nuclear Smads3/4 were occasionally observed in the extracellular matrix accumulated in capsular opacification. Exogenous TGFβ induced nuclear translocation of Smad3 in LECs of anterior capsule specimens in explant culture.</p>
<p>
<bold>Conclusions:</bold>
This is consistent with TGFβ induced Smad signalling being involved in regulating the behaviour of LECs during wound healing after cataract surgery.</p>
</div>
</front>
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<journal-id journal-id-type="nlm-ta">Br J Ophthalmol</journal-id>
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<article-id pub-id-type="pmc">1771405</article-id>
<article-id pub-id-type="publisher-id">0861428</article-id>
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<subj-group subj-group-type="heading">
<subject>Laboratory Science</subject>
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<title-group>
<article-title>TGFβ-Smad signalling in postoperative human lens epithelial cells</article-title>
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<name>
<surname>Saika</surname>
<given-names>S</given-names>
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<surname>Miyamoto</surname>
<given-names>T</given-names>
</name>
<xref ref-type="aff" rid="aff1">1</xref>
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<name>
<surname>Ishida</surname>
<given-names>I</given-names>
</name>
<xref ref-type="aff" rid="aff1">1</xref>
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<name>
<surname>Shirai</surname>
<given-names>K</given-names>
</name>
<xref ref-type="aff" rid="aff1">1</xref>
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<name>
<surname>Ohnishi</surname>
<given-names>Y</given-names>
</name>
<xref ref-type="aff" rid="aff1">1</xref>
</contrib>
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<name>
<surname>Ooshima</surname>
<given-names>A</given-names>
</name>
<xref ref-type="aff" rid="aff2">2</xref>
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Department of Ophthalmology, Wakayama Medical University, Wakayama, Japan</aff>
<aff id="aff2">
<label>2</label>
Department of Pathology, Wakayama Medical University, Wakayama, Japan</aff>
<aff id="aff3">
<label>3</label>
Save Sight Institute and Department of Anatomy and Histology, University of Sydney, Sydney, NSW, Australia</aff>
<author-notes>
<fn>
<p>Correspondence to: …Shizuya Saika, MD, PhD, Department of Ophthalmology, Wakayama Medical University, 811-1 Kimiidera, Wakayama, 641-0012, Japan; …
<email>shizuya@wakayama-med.ac.jp</email>
</p>
</fn>
</author-notes>
<pub-date pub-type="ppub">
<month>12</month>
<year>2002</year>
</pub-date>
<volume>86</volume>
<issue>12</issue>
<fpage>1428</fpage>
<lpage>1433</lpage>
<history>
<date date-type="accepted">
<day>17</day>
<month>7</month>
<year>2002</year>
</date>
</history>
<copyright-statement>Copyright © Copyright 2002 British Journal of Ophthalmology</copyright-statement>
<copyright-year>2002</copyright-year>
<abstract>
<p>
<bold>Aims:</bold>
To localise Smads3/4 proteins in lens epithelial cells (LECs) of fresh and postoperative human specimens. Smads3/4 are involved in signal transduction between transforming growth factor β (TGFβ) cell surface receptors and gene promoters. Nuclear localisation of Smads indicates achievement of endogenous TGFβ signalling in cells.</p>
<p>
<bold>Methods:</bold>
Three circular sections of the anterior capsule, one lens, and 17 capsules undergoing postoperative healing were studied. Immunohistochemistry was performed for Smads3/4 in paraffin sections of the specimens. The effect of exogenous TGFβ2 on Smad3 subcellular localisation was examined in explant cultures of extracted human anterior lens epithelium.</p>
<p>
<bold>Results:</bold>
The cytoplasm, but not the nuclei, of LECs of uninjured lenses was immunoreactive for Smads3/4. In contrast, nuclear immunoreactivity for Smads3/4 was detected in LECs during capsular healing. Nuclei positive for Smads3/4 were observed in monolayered LECs adjacent to the regenerated lens fibres of Sommerring’s ring. Interestingly, the nuclei of LECs that were somewhat elongated, and appeared to be differentiating into fibre-like cells, were negative for Smads3/4. Fibroblast-like, spindle-shaped lens cells with nuclear immunoreactivity for nuclear Smads3/4 were occasionally observed in the extracellular matrix accumulated in capsular opacification. Exogenous TGFβ induced nuclear translocation of Smad3 in LECs of anterior capsule specimens in explant culture.</p>
<p>
<bold>Conclusions:</bold>
This is consistent with TGFβ induced Smad signalling being involved in regulating the behaviour of LECs during wound healing after cataract surgery.</p>
</abstract>
<kwd-group>
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