May 2006
Volume 47, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2006
Regulation of ZENK mRNA Levels in the Chicken Retina by Duration of Light Exposure, by Image Quality and By Inter–Ocular Coupling
Author Affiliations & Notes
  • M.P. Feldkaemper
    Neurobiology, Univ. Eye Hospital Tuebingen, Germany, Tuebingen, Germany
  • V. Choh
    School of Optometry, Univ. of California, Berkeley, CA
  • F. Schaeffel
    Neurobiology, Univ. Eye Hospital Tuebingen, Germany, Tuebingen, Germany
  • C. Wildsoet
    School of Optometry, Univ. of California, Berkeley, CA
  • Footnotes
    Commercial Relationships  M.P. Feldkaemper, None; V. Choh, None; F. Schaeffel, None; C. Wildsoet, None.
  • Footnotes
    Support  German Research Council (DFG, FE 450/1–1) & the National Eye Institute (NEI R01 EY12392–06)
Investigative Ophthalmology & Visual Science May 2006, Vol.47, 1146. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      M.P. Feldkaemper, V. Choh, F. Schaeffel, C. Wildsoet; Regulation of ZENK mRNA Levels in the Chicken Retina by Duration of Light Exposure, by Image Quality and By Inter–Ocular Coupling . Invest. Ophthalmol. Vis. Sci. 2006;47(13):1146.

      Download citation file:


      © ARVO (1962-2015); The Authors (2016-present)

      ×
  • Supplements
Abstract

Purpose: : The number of ZENK expressing glucagonergic amacrine cells in the chick retina is controlled by the sign and amount of imposed defocus. In other amacrine cells and in bipolar cells, ZENK varies with the light exposure. Both eyes show changes in ZENK mRNA levels even when spectacle lenses are applied only to one eye. This apparent yoking persists even when the optic nerve of the lens–treated eye is cut (ONS). To investigate whether the duration of light exposure contributes to this yoking effect, the effect of diurnal cycle on ZENK mRNA levels was studied in normal and ONS birds.

Methods: : Retinal ZENK mRNA levels were measured in untreated control birds (n=21) and unilaterally ONS–sectioned birds (n=29). Tissues were harvested 3 to 7.5 hours after the light onset in the morning. In addition, another 33 chicks underwent unilateral ONS. Ten days later, –10 D spectacle lenses were attached to either the ONS–eye (n=17) or its fellow eye (n=16). Both eyes were harvested after 30 min (n=9, 8) or 2 hours (n=8, 8) of spectacle lens wear. An additional 18 chicks wore a lens over one eye and were harvested at the same times (n=9, 9). Transcriptional changes of ZENK were measured by real–time RT–PCR.

Results: : Retinal ZENK mRNA levels varied as a function of time of day (p=0.0084), with both untreated control and ONS eyes showing maximal levels in the morning (10:30 and 11:15 h) and declining to about 50% by mid–afternoon (14:15 and 15:00 h). Moreover, ZENK mRNA levels were reduced in ONS eyes (p=0.0033). Compared to fellow eyes, ZENK mRNA levels were lower in lens–treated normal (p=0.0013) and ONS–eyes (p<0.0001), after correction for the diurnal effects. ZENK levels in lens–wearing normal eyes were not different than their fellow ONS eyes.

Conclusions: : Diurnal light exposure significantly affects retinal ZENK mRNA levels. Moreover, ONS itself decreases retinal ZENK mRNA levels. This is unexpected, given that ONS eyes showed reduced axial growth, and that reduced retinal ZENK levels are normally typical for eyes that elongate and become myopic.

Keywords: myopia • retina • gene/expression 
×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×