May 2006
Volume 47, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2006
HIPKs Are Involved in Regulation of Retinal Cell Number and Lens Morphology
Author Affiliations & Notes
  • T. Inoue
    Kumamoto Univ Grad Sch Med, Kumamoto, Japan
    Ophthalmology and Visual Science,
  • T. Kagawa
    Kumamoto Univ Grad Sch Med, Kumamoto, Japan
    Cell Fate Modulation, Institute of Molecular Embryology and Genetics,
  • M.M. Inoue
    Kumamoto Univ Grad Sch Med, Kumamoto, Japan
    Cell Fate Modulation, Institute of Molecular Embryology and Genetics,
  • K. Isono
    Developmental Genetics, RIKEN Research Center for Allergy and Immunology, Yokohama, Japan
  • M. Fukushima
    Kumamoto Univ Grad Sch Med, Kumamoto, Japan
    Ophthalmology and Visual Science,
  • T. Taga
    Kumamoto Univ Grad Sch Med, Kumamoto, Japan
    Cell Fate Modulation, Institute of Molecular Embryology and Genetics,
  • H. Tanihara
    Kumamoto Univ Grad Sch Med, Kumamoto, Japan
    Ophthalmology and Visual Science,
  • Footnotes
    Commercial Relationships  T. Inoue, None; T. Kagawa, None; M.M. Inoue, None; K. Isono, None; M. Fukushima, None; T. Taga, None; H. Tanihara, None.
  • Footnotes
    Support  grant–in–aid for 21st Century COE
Investigative Ophthalmology & Visual Science May 2006, Vol.47, 2788. doi:
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      T. Inoue, T. Kagawa, M.M. Inoue, K. Isono, M. Fukushima, T. Taga, H. Tanihara; HIPKs Are Involved in Regulation of Retinal Cell Number and Lens Morphology . Invest. Ophthalmol. Vis. Sci. 2006;47(13):2788.

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

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Abstract

Purpose: : To investigate the function of homeodomain interacting protein kinase family proteins(HIPKs), HIPK1, HIPK2, and HIPK3, during mouse eye development.

Methods: : To examine the HIPKs expression pattern, RT–PCR analysis, immunohistochemical analysis, and in situ hybridization were performed. For functional analysis, single or double knock out mice of HIPK1 and HIPK2 were analyzed morphologically.

Results: : In the RT–PCR analysis,HIPK1 and HIPK2 were expressed during late embryogenesis. In the immunohistochemical analysis and in situ hybridization, HIPK2 was localized to the ganglion cell layer at E14.5. The eye of HIPK1+/– HIPK2–/– mouse showed decreased size, thickened retina and small lens as compared to the eye of wild type littermate. In addition, some of them showed colobomatous microphthalmia occupied by hyperplasic retina without lens, which was partially penetrant with 22 %.

Conclusions: : HIPKs are involved in regulation of retinal cell number and lens morphology during late embryogenesis.

Keywords: retinal development • apoptosis/cell death • development 
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