Active Infection & Immunity Brain & Nervous System

Modifying the gut microbiota to protect the ageing eye and brain.

In plain English

AI plain-English summary

A single transfer of gut microbes from young mice to old mice can reverse age-related inflammation in the brain and eye. As people live longer, rising rates of dementia and vision loss place growing strain on healthcare systems and families, yet current treatments target symptoms rather than the underlying ageing process. This project aims to identify exactly which microbes or microbial products drive the rejuvenating effects seen in the mouse experiments. If the key microbes or molecules can be pinned down, the work could lead to a dietary supplement or probiotic that modifies the gut microbiota in older adults to slow cognitive decline and protect against sight loss. Because the research is fundamental—it asks how gut microbes communicate with the immune system to influence the ageing brain and eye—any practical application would require further development. But similar fundamental discoveries about the gut-immune connection have already opened new avenues for treating inflammatory diseases, suggesting that understanding this axis could eventually yield interventions that keep both mind and vision sharper for longer.

View original technical description
As we age, cellular and molecular changes in the eye and the brain lead to worsening vision and memory, and increase our risk of developing dementias. This presents a huge public healthcare and economic challenge in our increasingly aged population. These age-associated changes are regulated by our immune system which in turn is strongly influenced by the vast community of microbes living within our gut (the gut microbiota). Changes in the composition and function of the gut microbiota have been linked with declining brain health, with recent studies implicating microbial modulation of signalling between the gut and the immune system (the ‘gut-immune-brain axis’). Growing evidence also supports a role for microbial involvement in age-associated eye diseases. I have recently shown that transferring gut microbiota from young donor mice to aged mice can reverse some of the detrimental inflammatory changes of ageing in the gut, the immune system, the brain, and the eye. In this proposal I will define which components of the microbiota transfers are responsible for these beneficial effects in aged recipients. Specifically, I will establish whether the whole microbiota community, specific microbes, or specific microbial products are responsible for improving brain and eye function and determine how they exert their effects. Ultimately, this work will establish how we can modify the aged gut microbiota to protect against both cognitive and visual decline in later life, and potentially protect people at risk from progression to sight loss and dementias.

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Researchers

Aimee Parker (Principal Investigator)

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Original classification

Fellowship

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