Injuries or diseases that kill retinal neurons and receptors block vision at it source. The lack of effective repair in the retina is a hallmark of the human nervous system; neurons that die are not replaced and functions that are lost are not recovered. This bleak outcome is a driving force for research on neural stem cells and the field of regeneration biology. The long-term objective of the project described in this proposal is to elucidate the molecular mechanisms that regulate persistent neurogenesis and injury-induced neuronal and photoreceptor regeneration in the retinas of teleost fish. The teleost retina is the only vertebrate CMS tissue where stem cells can regenerate a single neuronal type that integrates into an existing circuit or can regenerate all cell types that completely restore the original tissue. Investigating stem cell-based regeneration in the teleost retina will advance our knowledge of mechanisms that govern the ability of intrinsic stem cells to restore neural circuits in the injured brain. Further, this knowledge may guide the development of potential stem cell-based therapies to treat nervous system injuries and disease. In this proposal three Specific Aims are described, each directed toward revealing molecular mechanisms that regulate the differentiation, genesis and regeneration of photoreceptors.
In Specific Aim 1 experiments are described to test the hypothesis: that dying photoreceptors are transcriptionally active and express proteins that stimulate regeneration.
In Specific Aim 2 reverse genetic approaches will be used to test the hypothesis that the bHLH transcription factor, neuroD, regulates cone differentiation and the proliferation of rod progenitors.
In Specific Aim 3 the cellular expression of the growth factor progranulin-A will be characterized in the developing and regenerating retina, and reverse genetics will be used to test the hypothesis that progranulin-A regulates retinal neurogenesis. Together these specific aims represent a focused and integrated research program to test specific hypotheses of the cellular and molecular regulation of persistent arid injury-induced neurogenesis in the vertebrate nervous system. ? ?

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY007060-20
Application #
7465371
Study Section
Special Emphasis Panel (ZRG1-CB-G (90))
Program Officer
Greenwell, Thomas
Project Start
1987-05-01
Project End
2010-06-30
Budget Start
2008-07-01
Budget End
2010-06-30
Support Year
20
Fiscal Year
2008
Total Cost
$325,452
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Ophthalmology
Type
Schools of Medicine
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Walsh, Caroline E; Hitchcock, Peter F (2017) Progranulin regulates neurogenesis in the developing vertebrate retina. Dev Neurobiol 77:1114-1129
Gramage, Esther; D'Cruz, Travis; Taylor, Scott et al. (2015) Midkine-a protein localization in the developing and adult retina of the zebrafish and its function during photoreceptor regeneration. PLoS One 10:e0121789
Taylor, Scott M; Alvarez-Delfin, Karen; Saade, Carole J et al. (2015) The bHLH Transcription Factor NeuroD Governs Photoreceptor Genesis and Regeneration Through Delta-Notch Signaling. Invest Ophthalmol Vis Sci 56:7496-515
Gramage, E; Li, J; Hitchcock, P (2014) The expression and function of midkine in the vertebrate retina. Br J Pharmacol 171:913-23
Huang, Tao; Cui, Jianlin; Li, Lei et al. (2012) The role of microglia in the neurogenesis of zebrafish retina. Biochem Biophys Res Commun 421:214-20
Taylor, Scott; Chen, Jing; Luo, Jing et al. (2012) Light-induced photoreceptor degeneration in the retina of the zebrafish. Methods Mol Biol 884:247-54
Luo, Jing; Uribe, Rosa A; Hayton, Sarah et al. (2012) Midkine-A functions upstream of Id2a to regulate cell cycle kinetics in the developing vertebrate retina. Neural Dev 7:33
Thomas, Jennifer L; Ochocinska, Margaret J; Hitchcock, Peter F et al. (2012) Using the Tg(nrd:egfp)/albino zebrafish line to characterize in vivo expression of neurod. PLoS One 7:e29128
Ghosh, Amiya K; Murga-Zamalloa, Carlos A; Chan, Lansze et al. (2010) Human retinopathy-associated ciliary protein retinitis pigmentosa GTPase regulator mediates cilia-dependent vertebrate development. Hum Mol Genet 19:90-8
Craig, Sonya E L; Thummel, Ryan; Ahmed, Hafiz et al. (2010) The zebrafish galectin Drgal1-l2 is expressed by proliferating Muller glia and photoreceptor progenitors and regulates the regeneration of rod photoreceptors. Invest Ophthalmol Vis Sci 51:3244-52

Showing the most recent 10 out of 19 publications