April 2009
Volume 50, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2009
Regulation of Basic Fibroblast Growing Factor (bFGF) by Retinal Glial (Müller) Cells Under Severe Retinal Ischemia
Author Affiliations & Notes
  • Y. Yafai
    Eye Hospital, University of Leipzig, Leipzig, Germany
  • I. Iandiev
    Eye Hospital, University of Leipzig, Leipzig, Germany
  • J. Lange
    Eye Hospital, University of Leipzig, Leipzig, Germany
  • W. Eichler
    Eye Hospital, University of Leipzig, Leipzig, Germany
  • A. Bringmann
    Eye Hospital, University of Leipzig, Leipzig, Germany
  • P. Wiedemann
    Eye Hospital, University of Leipzig, Leipzig, Germany
  • Footnotes
    Commercial Relationships  Y. Yafai, None; I. Iandiev, None; J. Lange, None; W. Eichler, None; A. Bringmann, None; P. Wiedemann, None.
  • Footnotes
    Support  None.
Investigative Ophthalmology & Visual Science April 2009, Vol.50, 2926. doi:
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      Y. Yafai, I. Iandiev, J. Lange, W. Eichler, A. Bringmann, P. Wiedemann; Regulation of Basic Fibroblast Growing Factor (bFGF) by Retinal Glial (Müller) Cells Under Severe Retinal Ischemia. Invest. Ophthalmol. Vis. Sci. 2009;50(13):2926.

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Abstract

Purpose: : To determine the regulation of basic fibroblast growth factor (bFGF) in glial (Müller) cells under conditions of ischemic/ hypoxic retinopathy.

Methods: : Transient retinal ischemia was induced in rat eyes by raising the intraocular pressure above the systolic pressure, and bFGF was determined in the retina. Furthermore, bFGF was investigated in surgically excised retinal tissues of patients with ischemic diabetic retinopathy, and using primary guinea-pig Müller cell cultures exposed to hypoxia. bFGF expression and secretion were studied by immunohistochemistry, real-time RT-PCR, and ELISA.

Results: : Retinal Müller cells demonstrated an increased level of bFGF immunoreactivity in fibrovascular tissues from patients with diabetes compared with retinal tissues from subjects with non-hypoxic pathologic myopia. In the ischemic rat retina, Müller cells contributed significantly to bFGF release when compared to non-ischemic retina. In Müller cell cultures severe hypoxia (0% O2) induced an increase of bFGF mRNA and protein levels. However, there was no effect on bFGF production in mild hypoxia (5% O2).

Conclusions: : These results suggest that Müller cells produce and secrete bFGF under certain conditions including severe hypoxia. The angiogenic activity of Müller cell-derived bFGF may contribute to the neovascular process in the retinal tissue in diabetic proliferative retinopathy.

Keywords: retinal neovascularization • choroid: neovascularization • glia 
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