The overall goal of this grant is to seek molecular therapies for diseases resulting from defects of the mitochondrial oxidative phosphorylation system. Complex I is the first of five enzyme complexes that comprise the oxidative phosphorylation system. It has the most intricate structure with 45 different subunits (of these, 7 subunits are mitochondrially encoded (designated ND1-6 and 4L)), one FMN and eight iron- sulfur clusters as cofactors. Complex I defects are involved in many human mitochondrial diseases. Leber's hereditary optic neuropathy (LHON) is recognized as the frequently occurring complex I disease. A new animal model has been developed that involves infusion of rotenone-biobeads into the superior colliculus of the rat brain. Symptoms typical of LHON were observed in the animals, most notably, severely impaired vision. At the same time, there was clearly disorganization of the node of Ranvier as well as demyelination of the RGC axons. However, loss of vision was not accompanied by the hallmarks of LHON such as thinner retinal ganglion cell (RGC) layer and death of RGC which only occurred at a later stage. Furthermore, delivery of the yeast alternative NADH dehydrogenase gene (NDI1) into the rat brain restored the vision to normal level with concomitant reorganization of the node of Ranvier and remyelination of the RGC axons. These findings form the basis of this research project. During this grant term, focus will be made on LHON research with the following specific aims. (i) To investigate mechanism of LHON by using the rat models by administration of mutated human or rat ND4 gene to the retina or rotenone biobeads infusion in the superior colliculus. (ii) To clarify whether the NDI1 gene expression can repair vision loss of the two LHON models and to determine repair window. (iii) To construct transgenic mouse strains carrying the mutated human or mouse ND4 gene for further investigation of LHON such as triggering factors.

Public Health Relevance

Mitochondria are referred to as the powerhouse of human body. Dysfunction of the enzymes in mitochondria causes many human diseases. This project is concerned with clarifying the mechanism of mitochondrial diseases and developing therapies by using the knowledge from the research.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY020796-15
Application #
8212077
Study Section
Neural Oxidative Metabolism and Death Study Section (NOMD)
Program Officer
Chin, Hemin R
Project Start
2011-02-01
Project End
2016-01-31
Budget Start
2012-02-01
Budget End
2013-01-31
Support Year
15
Fiscal Year
2012
Total Cost
$472,616
Indirect Cost
$222,616
Name
Scripps Research Institute
Department
Type
DUNS #
781613492
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Marella, Mathieu; Patki, Gaurav; Matsuno-Yagi, Akemi et al. (2013) Complex I inhibition in the visual pathway induces disorganization of the node of Ranvier. Neurobiol Dis 58:281-8
Marella, Mathieu; Seo, Byoung Boo; Flotte, Terence R et al. (2011) No immune responses by the expression of the yeast Ndi1 protein in rats. PLoS One 6:e25910