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Leading the Fight to treat and cure
Tay-Sachs, Canavan, Sandhoff, GM1 and related diseases

2018 Research Initiative Grants

NTSAD is proud to make three grant awards to the talented investigators and their institutions. Information about their grants is described below. This year’s grants are for Sandhoff/Tay-Sachs and GM-1 diseases, our goal is to advance research towards treatments for all of our diseases.


Alessandra D'Azzo, PhD
St. Jude's Children's Research Hospital

Role of Plasma membrane-ER Contact Sites in 
GM1-mediated Neuronal Cell Death

GM1-gangliosidosis is a neurodegenerative lysosomal storage disorder that presents with a spectrum of severity. It is caused by genetic mutations in the B-Gal gene that affect the expression and/or function of the B-Gal enzyme, leading to impaired degradation of one of its major target substrates, GM1-ganglioside (GM1). GM1 is particularly abundant in the nervous system, because it is a major component of neuronal outer membranes. Thus, the direct consequence of B-Gal deficiency is the relentless and progressive accumulation of GM1 in lysosomes and other subcellular membranes, which leads to the death of neurons, neuroinflammation and neurodegeneration. A deep understanding of the cellular and molecular events downstream of B-Gal loss of function and GM1 accumulation may give us the chance to identify alternative ways to tackle the disease therapeutically or provide us with appropriate end points to assess the extent of functional reversal of phenotypic abnormalities after treatment. 

With these studies we plan to evaluate in the mouse model of GM1-gangliosidosis how GM1 accumulation affects the membrane contact sites formed between cellular components and the neuronal outer membranes. In particular, we will analyze the protein and lipid components of these membrane contact sites in order to assess whether they are altered by abnormal local concentrations of calcium ions caused by the accumulated GM1. This will help us to understand the role of calcium and calcium-binding proteins at these contact sites in causing the damage to neurons. We will perform therapeutic proof of principle studies aimed to inhibit the function of a specific calcium-binding protein, which, if successful, may set the foundation for a novel therapeutic approach for the treatment of
this lysosomal disease in children.


Tony Futerman, PhD
Weizmann Institute of Science (Israel)

Role of microglia in Sandhoff disease pathology


Microglia are inflammatory cells found in the central nervous system. They are known to play a role in the pathophysiology of Sandhoff disease but the inflammatory pathways activated are not known. This study aims to better understand these pathways to delineate potential targets for therapeutic intervention in Sandhoff and Tay-Sachs diseases.

This lab has a record of success identifying pathways that might be amenable to therapeutic intervention in other lysosomal storage diseases.


Xuntian Jiang,PhD
Washington University School of Medicine (St. Louis, MO)

Oligosaccharide Biomarkers for Disease Progression and AAV Therapeutic Efficacy in GM1 Gangliosidosis

A major challenge for developing treatments for GM1 gangliosidosis (GM1) disease is difficulty in evaluation of efficacy. This is complicated by limited patient numbers, and variability in age, severity, and stage of disease progression. Biomarkers that reflect disease status could provide a valuable surrogate endpoint for assessment of treatment effect and reasonably predict clinical benefit. We have identified an oligosaccharide  (carbohydrate whose molecule is composed of a relatively small number of monosaccharides) biomarker that is significantly elevated in the urine, cerebrospinal fluid (CSF) and plasma from GM1 patients and brains from GM1 cat model. This biomarker in GM1 cat brains was reduced in response to gene therapy. These results suggest that the oligosaccharide is a sensitive biomarker for disease severity and progression and for assessing treatment efficacy. In this proposal, we will identify the structure of the oligosaccharide biomarker and evaluate this marker as a surrogate outcome measure of treatment for GM1. This project will provide a much-needed tool for assessing GM1 disease severity and therapeutic efficacy.


 

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