Both acidic and basic forms of fibroblast growth factor (aFGF and bFGF) have inductive effects on lens epithelial cells in culture. There is also evidence that FGF is present in various ocular tissues, including some lens epithelial cells. The central hypothesis of this project is that FGF plays a key role in events in lens development, including morphogenesis, growth and maintenance. The project has two primary aims: (1) To determine which lens cells are (or likely to be) exposed to FGF during embryonic and postnatal development. Specific questions are: (a) What is the distribution of FGF in the eye? Immunolocalization of aFGF and bFGF in lens and associated tissues will be carried out using rats of various embryonic and postnatal stages of development; (b) Where is FGF produced in the eye? At the same developmental stages, mRNA for aFGF and bFGF will be localized by in situ hybridization; (2) To examine the functional significance of FGF (whether produced by lens cells or outside the lens) in the lens. Specific questions are: (a) Does lens-derived FGF have biological activity? Proliferative responses of explants exposed to lens-conditioned medium (with or without FGF antibodies) will be determined; (b) Is there a relationship between patterns of cell proliferation and FGF distribution in the lens? Immunohistochemistry will be used to quantify and compare spatial patterns of proliferation and FGF distribution in lenses throughout development. In some experiments cultured lenses will also be used; (c) Is cell proliferation in the lens blocked by FGF inhibitors? The effects of specific antibodies and other inhibitors on spatial patterns of proliferation in cultured lenses will be assessed as in previous section; (d) Does vitreous contain more FGF than aqueous? FGF activity will be assessed using lens explants and standard assay including immunoneutralization; aFGF and bFGF will also be quantified by ELISA; (e) Does exposure to FGF induce central epithelial cells to behave like peripheral cells? A combination of techniques already described will be used. This work is fundamental to understanding how the normal lens forms, grows and is maintained throughout life. This is important for understanding the nature of developmental abnormalities, including growth abnormalities, and may also provide the basis for understanding at least some of the subtle changes that lead to cataract.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY003177-15
Application #
2158638
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1991-09-30
Project End
1995-05-31
Budget Start
1993-09-30
Budget End
1995-05-31
Support Year
15
Fiscal Year
1993
Total Cost
Indirect Cost
Name
University of Sydney
Department
Type
DUNS #
752389338
City
Sydney
State
Country
Australia
Zip Code
2006
Dawes, L J; Shelley, E J; McAvoy, J W et al. (2018) A role for Hippo/YAP-signaling in FGF-induced lens epithelial cell proliferation and fibre differentiation. Exp Eye Res 169:122-133
Zhao, Guannan; Bailey, Charles G; Feng, Yue et al. (2018) Negative regulation of lens fiber cell differentiation by RTK antagonists Spry and Spred. Exp Eye Res 170:148-159
Shu, Daisy Y; Wojciechowski, Magdalena C; Lovicu, Frank J (2017) Bone Morphogenetic Protein-7 Suppresses TGF?2-Induced Epithelial-Mesenchymal Transition in the Lens: Implications for Cataract Prevention. Invest Ophthalmol Vis Sci 58:781-796
Wojciechowski, Magdalena C; Mahmutovic, Leila; Shu, Daisy Y et al. (2017) ERK1/2 signaling is required for the initiation but not progression of TGF?-induced lens epithelial to mesenchymal transition (EMT). Exp Eye Res 159:98-113
McAvoy, J W; Dawes, L J; Sugiyama, Y et al. (2017) Intrinsic and extrinsic regulatory mechanisms are required to form and maintain a lens of the correct size and shape. Exp Eye Res 156:34-40
Shu, Daisy Y; Lovicu, Frank J (2017) Myofibroblast transdifferentiation: The dark force in ocular wound healing and fibrosis. Prog Retin Eye Res 60:44-65
Das, Shannon J; Lovicu, Frank J; Collinson, Emma J (2016) Nox4 Plays a Role in TGF-?-Dependent Lens Epithelial to Mesenchymal Transition. Invest Ophthalmol Vis Sci 57:3665-73
Lovicu, F J; Shin, E H; McAvoy, J W (2016) Fibrosis in the lens. Sprouty regulation of TGF?-signaling prevents lens EMT leading to cataract. Exp Eye Res 142:92-101
Audette, Dylan S; Anand, Deepti; So, Tammy et al. (2016) Prox1 and fibroblast growth factor receptors form a novel regulatory loop controlling lens fiber differentiation and gene expression. Development 143:318-28
Sugiyama, Yuki; Shelley, Elizabeth J; Yoder, Bradley K et al. (2016) Non-essential role for cilia in coordinating precise alignment of lens fibres. Mech Dev 139:10-7

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