Dr. Jan Kaslin, from the Australian Regenerative Medicine Institute (ARMI), based at Monash University, Australia, has developed the world’s first zebrafish model for Sanfilippo Syndrome with the support of a grant from Cure Sanfilippo Foundation and Sanfilippo Children’s Foundation (Australia).
The zebrafish model of Sanfilippo type A represents a powerful tool for researchers to gain a greater understanding of the disease mechanisms and help advance new therapies.
The devastating effects seen in Sanfilippo stem from an enzyme deficiency that leads to the build-up of heparan sulfate. In Sanfilippo type A, the enzyme involved is called sulfamidase, or SGSH. While the clinical features of the disease are well-known, more research is needed on the effects of Sanfilippo on cells and tissues to help reveal new ways to treat it.
Zebrafish are a powerful model organism in medical research to study disease, from the cellular level to its effects on the whole organism. It is cheaper and easier to breed zebrafish compared to mice models, they can produce hundreds of offspring to study in a very short space of time, and there are many tools readily available to study them.
Initial results from the first Sanfilippo zebrafish model
In the study, which has just been published in the International Journal of Molecular Science, Dr. Kaslin and his team created a zebrafish unable to produce a functional SGSH enzyme. This led to a build-up of heparan sulfate in the tissues, especially the brains, of the Sanfilippo zebrafish over time.
When brain cells of young and older Sanfilippo fish were studied under high-powered microscopes, there were abnormalities seen inside the cells, such as large numbers of swollen lysosomes, where heparan sulphate accumulates, as are seen in the cells of children with Sanfilippo. The team also observed large numbers of dying brain cells in young Sanfilippo zebrafish, potentially due to unrepairable cellular damage.
The researchers assessed the behavior of young and older Sanfilippo zebrafish. In young fish two days after hatching (when nervous system development is near completion), the Sanfilippo zebrafish were more hyperactive compared to unaffected fish. This was reversed in six-month-old adult fish, where the Sanfilippo zebrafish showed less activity than the unaffected zebrafish, as well as behavior indicative of cognitive decline.
Inflammation in the brain of the zebrafish model was also investigated as this has been shown to be a potentially important part of the disease biology in Sanfilippo and other neurodegenerative diseases. Compared to unaffected fish, young Sanfilippo zebrafish developed severe brain inflammation and activation of microglia, important immune cells in the brain. These features were also observed in adults, indicating sustained brain inflammation throughout the life of the Sanfilippo zebrafish.
When an important inflammatory pathway was blocked using a drug, visible signs of inflammation in the brain were reduced in young Sanfilippo zebrafish. Long-term anti-inflammatory treatment in young fish also rescued some aspects of the behavioral symptoms seen in the fish during resting conditions, but not in stressful conditions. This suggests that inflammation might lie behind some of the symptoms seen in individuals with Sanfilippo syndrome, but not others, and needs further investigation.
Impact on the future of Sanfilippo research
The zebrafish model of Sanfilippo mirrors the disease seen in patients, giving researchers a very helpful new tool to study the condition. This will provide a better understanding of Sanfilippo overall, how it affects the cells of the brain, and will help the identification and testing of new therapies. By adding a zebrafish model to the toolbox for Sanfilippo research, we are one step closer to finding therapies for patients.
Content Source: Sanfilippo Children’s Foundation
Project Grant: Creating a Zebrafish Model of Sanfilippo Syndrome Type A
Peer-Reviewed Article: “An Engineered sgsh Mutant Zebrafish Recapitulates Molecular and Behavioural Pathobiology of Sanfilippo Syndrome A/MPS IIIA” in International Journal of Molecular Science