The proposed experiments are aimed at furthering our understanding of regeneration through knock- outs of particular pathways and combinations of pathways in mice. The purposes of our experiments are threefold: 1) to identify the isolation or interaction of pathways that may contribute to regeneration, 2) to provide indication for and identify potential side-effects of specific therapeutic targeting and their combinatorial targeting, and 3) to establish lines of mice with dramatically enhanced regeneration for further scientific research. The bases of these experiments come from 3 recent developments of observations of remarkable regeneration in mice or disinhibition in-culture: regeneration in PTEN mice, regeneration in PDE8 mice, and myelin- and Nogo-disinhibition of neurons lacking function of both Nogo co-receptors. Specifically in our experiments we will assess for regeneration in mice lacking both Nogo co-receptors, create and assess the regenerative ability of mice lacking PTEN and one of the Nogo co-receptors, and create triple knock-out mice lacking both Nogo co-receptors and PDE8 or PTEN, and assess for combinatorial effects on regeneration. By combining knock-outs of these mice, we will be able to assess these pathways for their combined involvement in regeneration after spinal cord injury (SCI), and it may result in producing more regeneration than was ever before possible. Additionally, we will characterize regeneration using a novel and powerful 3D technique that allows visualization of whole volumes of tissue without physical cutting, potentially revolutionizing the field for how regeneration is analyzed. Clinically, this work aims to accelerate the translation of basic science to therapeutic applications for SCI, potentially by identifying combinatorial therapeutic strategies, identifying new targets, and streamlining drug development by ruling out approaches that are found to not be promising. Furthermore, the pursuit of these projects and the use of these techniques will foster the scientific development of Mr. Rafer Willenberg, providing him excellent training for a future scientific career.

Public Health Relevance

This project aims to identify combinations of molecular pathways that may be targeted to stimulate regeneration following spinal cord injury. Identifying these combined targets should help to point out the types of drugs and combinations of drugs that may have the greatest benefits.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31NS070558-03
Application #
8230527
Study Section
Special Emphasis Panel (ZRG1-ETTN-G (29))
Program Officer
Owens, David F
Project Start
2010-03-01
Project End
2013-02-28
Budget Start
2012-03-01
Budget End
2013-02-28
Support Year
3
Fiscal Year
2012
Total Cost
$36,549
Indirect Cost
Name
University of California Irvine
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
046705849
City
Irvine
State
CA
Country
United States
Zip Code
92697
Liu, Kai; Lu, Yi; Lee, Jae K et al. (2010) PTEN deletion enhances the regenerative ability of adult corticospinal neurons. Nat Neurosci 13:1075-81