In humans, vision is the most important sense and damage to the retina or the optic nerve can cause irreversible vision loss. This is because the retina and the optic nerve are part of the central nervous system (CNS), which in adult mammals has lost its regenerative capacity. In contrast, amphibians and fish, including zebrafish, have retained a remarkable capacity to generate new CNS neurons, and to re-grow severed or damage axons and nerves, including the optic nerve. The optic nerve, which conveys visual information from the retina into the brain contains axons from only one retinal cell type, the retinal ganglion cells (RGC). After optic nerve transection, zebrafish RGC neurons survive, and -independently of neurogenesis- regrow axons to their original synaptic targets where they form functional synapses. Surprisingly, the molecular genetic pathways for this remarkable capacity to regenerate axons in vivo, are not well understood. Here, I propose to take advantage of this regenerative capacity and to perform a genetic and a small molecule screens to identify genes and pathways required for optic nerve regeneration in vivo. We have chosen this system because it is very accessible to simple, rapid and reproducible nerve transection amiable to screens, because of our longstanding interest and expertise in visual system development and function, and because all findings regarding regeneration in the visual are also translatable to CNS regeneration in general. The long term-goal of this research proposal is to define the genetic, molecular and cellular pathways underlying axonal regeneration. The experiments in this proposal will: (1) screen an equivalent of ~970 chemically mutagenized genomes for defects specifically in optic nerve axonal regeneration; (2) identify the molecular nature of at least 30 mutants (through a whole genome sequencing approach); and (3) perform a small molecule pilot screen of 1760 small molecules with known targets to identify factors that delay axon fragmentation, and de- or increase optic nerve axonal regeneration to define entry points into pathways underlying axonal regeneration. These studies are relevant to the study of human diseases that cause damage to the optic nerve, including hereditary optic neuropathies, cancer or multiple sclerosis as well conditions of increased intraocular pressure which can cause irreversible optic nerve degeneration and vision loss. Given the current lack of therapeutic interventions for optic nerve damage or for spinal cord injury in general, we propose to apply a more unbiased genetic approach to determine the molecular mechanisms underlying axonal regeneration, and to exploit these mechanisms towards the development of therapeutic strategies in mammals.

Public Health Relevance

In contrast to mammals, fish have the impressive regenerative capacity to regenerate transected CNS axons and nerves including the optic nerve. Given the success of genetic screens in invertebrates, and that unbiased screens for axonal regeneration have not been reported in vertebrates, we propose to perform small molecule and genetic screens for genes and pathways critical optic nerve regeneration in vivo. This is directly relevant to the study of human vision, because damage to the optic nerve by diseases such as hereditary neuropathies, cancer or multiple sclerosis but also by increased intraocular pressure, can cause irreversible vision loss.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY024861-02
Application #
8895957
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Chin, Hemin R
Project Start
2014-08-01
Project End
2019-06-30
Budget Start
2015-07-01
Budget End
2016-06-30
Support Year
2
Fiscal Year
2015
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Gribble, Katherine D; Walker, Lauren J; Saint-Amant, Louis et al. (2018) The synaptic receptor Lrp4 promotes peripheral nerve regeneration. Nat Commun 9:2389
Bremer, Juliane; Granato, Michael (2016) Myosin phosphatase Fine-tunes Zebrafish Motoneuron Position during Axonogenesis. PLoS Genet 12:e1006440
Banerjee, Santanu; Hayer, Katharina; Hogenesch, John B et al. (2015) Zebrafish foxc1a drives appendage-specific neural circuit development. Development 142:753-62
Marsden, Kurt C; Granato, Michael (2015) In Vivo Ca(2+) Imaging Reveals that Decreased Dendritic Excitability Drives Startle Habituation. Cell Rep 13:1733-40
Isaacman-Beck, Jesse; Schneider, Valerie; Franzini-Armstrong, Clara et al. (2015) The lh3 Glycosyltransferase Directs Target-Selective Peripheral Nerve Regeneration. Neuron 88:691-703
Rosenberg, Allison F; Isaacman-Beck, Jesse; Franzini-Armstrong, Clara et al. (2014) Schwann cells and deleted in colorectal carcinoma direct regenerating motor axons towards their original path. J Neurosci 34:14668-81