June 2013
Volume 54, Issue 15
Free
ARVO Annual Meeting Abstract  |   June 2013
Evaluation of MicroRNA Expression Profiles for Form-Deprivation Myopia in Mouse
Author Affiliations & Notes
  • Xiaoyan Luo
    Department of Ophthalmology, Duke University, Durham, NC
    Duke Center for Human Genetics, Duke University Medical Center, Durham, NC
  • Tatiana Tkatchenko
    Department of Anatomy & Cell Biology, Wayne State University, Detroit, MI
  • Andrei Tkatchenko
    Department of Anatomy & Cell Biology, Wayne State University, Detroit, MI
    Department of Ophthalmology, Wayne State University, Detroit, MI
  • Ravikanth Metlapally
    School of Optometry, University of California at Berkeley, Berkeley, CA
  • Pedro Gonzalez
    Department of Ophthalmology, Duke University, Durham, NC
  • Terri Young
    Department of Ophthalmology, Duke University, Durham, NC
    Duke Center for Human Genetics, Duke University Medical Center, Durham, NC
  • Footnotes
    Commercial Relationships Xiaoyan Luo, None; Tatiana Tkatchenko, None; Andrei Tkatchenko, None; Ravikanth Metlapally, None; Pedro Gonzalez, None; Terri Young, National Institutes of Health (F)
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2013, Vol.54, 3673. doi:
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      Xiaoyan Luo, Tatiana Tkatchenko, Andrei Tkatchenko, Ravikanth Metlapally, Pedro Gonzalez, Terri Young, ; Evaluation of MicroRNA Expression Profiles for Form-Deprivation Myopia in Mouse. Invest. Ophthalmol. Vis. Sci. 2013;54(15):3673.

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

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Abstract

Purpose: The study aim was to determine microRNA (miRNA) expression profiles of ocular tissues in form-deprivation induced myopic mice.

Methods: Fifteen C57BL/6J mice (Jackson Laboratory, Bar Harbor, ME) were used in this study. Form-deprivation myopia was induced in postnatal day 24 (P24) C57BL/6J mice by applying a frosted hemispherical plastic diffuser over the right eye for 10 days. Total RNA was isolated from the whole eye, retina, and sclera and used for miRNA expression profiling with the Agilent mouse miRNA microarray(Agilent Technologies, Inc., Santa Clara, CA). The microarray raw data were processed by subtracting background noise and performing log2 transformation. Sample outliers were removed. The normalized microarray data were analyzed using ANOVA to identify differences in miRNA expression level between myopic and contralateral control eyes.

Results: ANOVA revealed 75 miRNAs with differential expressions [fold change (FC) >= 1.5] from the whole eye, retina, and sclera. Multiple members of the miRNA family -302 (b and c), -466 (c, g, h, and j), and -669 (a, b, e, and o), and three members of the 290-295 cluster (290, 291 and 294) showed increased or decreased differential expressions. Member examples included mmu-miR-302c [FC= 3.2; p=2.1E-2], mmu-miR-466c [FC=2.3; p=2.0E-3], mmu-miR-466j [FC=3.1; p=8.5E-4], and mmu-miR-669b [FC=2.1; p=9.0E-4] from the whole eye; mmu-miR-294 [FC=1.5; p= 2.4E-2] and [FC=2.3; p=8.0E-5] from retina and sclera separately. MiR-302 and the 290-295 member cluster are involved in cell pluripotency maintenance. Other differentially expressed miRNA examples included mmu-miR-15a [FC=2.2; p=1.1E-3] and mmu-miR-16-1[FC=2.1; p=4.6E-4] from the whole eye, and mmu-miR-21[FC=2.2; p=1.7E-3] from retina. MiR-15, 16, and 21 are involved in growth and development regulation.

Conclusions: Differential expression of miRNAs in several ocular tissues upon induction of experimental myopia in mice suggests a developmental and regulatory role in eye growth, and can potentially serve as therapeutic targets for treating myopia.

Keywords: 605 myopia • 708 sclera • 535 gene microarray  
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