Literature DB >> 15343149

Early transcriptional changes of retinal and choroidal TGFbeta-2, RALDH-2, and ZENK following imposed positive and negative defocus in chickens.

Perikles Simon1, Marita Feldkaemper, Michaela Bitzer, Sibylle Ohngemach, Frank Schaeffel.   

Abstract

PURPOSE: Imposing defocus to the retina results in compensatory changes of axial eye growth. It is not clear which factors initially contribute to this process and whether they act on the post-translational, translational, or transcriptional level. We have measured early changes in mRNA levels, in response to imposed negative and positive defocus, of the transcription factor ZENK, the retinoic acid synthesis enzyme RALDH-2, and the growth factor TGFbeta-2.
METHODS: Chickens 11 days of age were unilaterally treated with positive or negative spectacle lenses of 7 D power. After 0, 15, 30, and 120 min, mRNA was extracted from retina and choroid, and the concentration of the mRNAs of the three candidates was measured by quantitative real time PCR in both eyes.
RESULTS: ZENK in the retina and RALDH-2 in the choroid displayed parallel signs of defocus dependent changes in mRNA levels after 15 or 30 min, respectively. ZENK mRNA levels were reduced in the retina after 15 min with both types of lenses but were then up regulated at 30 min with positive lenses and down regulated with negative lenses, similar to the previously observed changes in ZENK protein levels. Changes of RALDH-2 and TGFbeta-2 mRNA levels were confined to the choroid. Treatment with negative lenses resulted in a rapid (15 min) and persistent decrease in TGFbeta-2 mRNA concentration in the choroid. Negative lenses provoked parallel but less pronounced alterations in the open fellow eyes.
CONCLUSIONS: Imposed defocus triggers extensive transcriptional changes of ZENK in the retina, and of TGFbeta-2 and RALHD-2 in the choroid. Changes in retina and choroid are rapid, show no phase delay with respect to each other, and can be considered, in the case of RALDH-2 and ZENK, as specific for the sign of imposed defocus. They occur prior to any morphological changes. This is consistent with a role in causing or controlling later changes in eye growth.

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Year:  2004        PMID: 15343149

Source DB:  PubMed          Journal:  Mol Vis        ISSN: 1090-0535            Impact factor:   2.367


  20 in total

1.  Change in the synthesis rates of ocular retinoic acid and scleral glycosaminoglycan during experimentally altered eye growth in marmosets.

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Review 2.  RPE and Choroid Mechanisms Underlying Ocular Growth and Myopia.

Authors:  Yan Zhang; Christine F Wildsoet
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3.  Effects of foveal ablation on emmetropization and form-deprivation myopia.

Authors:  Earl L Smith; Ramkumar Ramamirtham; Ying Qiao-Grider; Li-Fang Hung; Juan Huang; Chea-su Kee; David Coats; Evelyn Paysse
Journal:  Invest Ophthalmol Vis Sci       Date:  2007-09       Impact factor: 4.799

4.  Studies on retinal mechanisms possibly related to myopia inhibition by atropine in the chicken.

Authors:  Ute Mathis; Marita Feldkaemper; Min Wang; Frank Schaeffel
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2019-12-26       Impact factor: 3.117

Review 5.  The dynamic sclera: extracellular matrix remodeling in normal ocular growth and myopia development.

Authors:  Angelica R Harper; Jody A Summers
Journal:  Exp Eye Res       Date:  2015-04       Impact factor: 3.467

Review 6.  Gene profiling in experimental models of eye growth: clues to myopia pathogenesis.

Authors:  Richard A Stone; Tejvir S Khurana
Journal:  Vision Res       Date:  2010-04-02       Impact factor: 1.886

7.  Image defocus and altered retinal gene expression in chick: clues to the pathogenesis of ametropia.

Authors:  Richard A Stone; Alice M McGlinn; Donald A Baldwin; John W Tobias; P Michael Iuvone; Tejvir S Khurana
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-07-29       Impact factor: 4.799

Review 8.  The choroid as a sclera growth regulator.

Authors:  Jody A Summers
Journal:  Exp Eye Res       Date:  2013-03-23       Impact factor: 3.467

9.  All-trans retinoic acid regulates the expression of the extracellular matrix protein fibulin-1 in the guinea pig sclera and human scleral fibroblasts.

Authors:  Chuanxu Li; Sally A McFadden; Ian Morgan; Dongmei Cui; Jianmin Hu; Wenjuan Wan; Junwen Zeng
Journal:  Mol Vis       Date:  2010-04-15       Impact factor: 2.367

10.  Alterations in ZENK and glucagon RNA transcript expression during increased ocular growth in chickens.

Authors:  Regan Ashby; Peter Kozulin; Pam L Megaw; Ian G Morgan
Journal:  Mol Vis       Date:  2010-04-13       Impact factor: 2.367

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