Split-scene illustration of UCSF mouse study: older mouse struggles in maze with poor hippocampal neural links due to FTL1; treated mouse excels with enhanced connections.
Split-scene illustration of UCSF mouse study: older mouse struggles in maze with poor hippocampal neural links due to FTL1; treated mouse excels with enhanced connections.
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UCSF study links iron-associated protein FTL1 to age-related memory decline in mice

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Researchers at the University of California, San Francisco report that higher levels of the iron-associated protein FTL1 in the hippocampus of older mice are tied to weaker neural connections and worse performance on cognitive tests. In the experiments, reducing FTL1 in older mice was associated with increased neuronal connectivity and improved memory performance, findings published in Nature Aging.

Scientists at the University of California, San Francisco tracked changes in genes and proteins in the hippocampus of mice as they aged and identified FTL1 as the protein that most consistently differed between young and old animals, according to a research summary released by the university.

In older mice, the researchers reported higher levels of FTL1 alongside fewer connections between neurons in the hippocampus and poorer performance on cognitive tests. In a separate set of experiments, boosting FTL1 in young mice caused the animals’ brains and behavior to resemble those of older mice. In lab experiments, neurons engineered to produce high amounts of FTL1 developed simplified structures, forming shorter, less complex extensions.

The team also reported a metabolic link: higher FTL1 levels in older mice were associated with slower cellular metabolism in the hippocampus. When researchers treated cells with a compound described as boosting metabolism, they found the negative effects were prevented.

The most dramatic effects were reported when FTL1 was reduced in older mice. The researchers said connections between brain cells increased and performance on memory tests improved.

“It is truly a reversal of impairments,” said Saul Villeda, PhD, associate director of the UCSF Bakar Aging Research Institute and senior author of the paper. “It’s much more than merely delaying or preventing symptoms.”

Villeda said the work could point to future approaches aimed at countering age-related brain decline. “We’re seeing more opportunities to alleviate the worst consequences of old age,” he said. “It’s a hopeful time to be working on the biology of aging.”

The paper is titled “Targeting iron-associated protein Ftl1 in the brain of old mice improves age-related cognitive impairment,” and was published in Nature Aging. The university said the work was funded in part by the Simons Foundation, the Bakar Family Foundation, the National Science Foundation, the Hillblom Foundation, the Bakar Aging Research Institute, Marc and Lynne Benioff, and the National Institutes of Health.

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Early discussions on X about the UCSF study express optimism regarding the reversal of age-related memory decline in mice by reducing FTL1 protein levels, with users summarizing the findings on improved neural connectivity and cognitive performance. Some highlight therapeutic potential for human aging, while others note the need for caution on applicability to humans. Reactions are mostly neutral to positive from science enthusiasts and regular users.

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Scientific illustration depicting healthy and damaged tanycytes in the brain's third ventricle clearing tau protein in Alzheimer’s disease.
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Study links tanycyte damage to reduced tau clearance in Alzheimer’s disease

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Researchers at UCLA Health and UC San Francisco have identified a natural defense mechanism in brain cells that helps remove toxic tau protein, potentially explaining why some neurons resist Alzheimer's damage better than others. The study, published in Cell, used CRISPR screening on lab-grown human neurons to uncover this system. Findings suggest new therapeutic avenues for neurodegenerative diseases.

Researchers at Marshall University report that microscopic particles found in the gut lumen—known as exosomes—differ between young and old mice and can influence metabolism and gut-barrier function when transferred between animals. The findings, published in the journal Aging Cell, suggest these particles may help drive biological changes associated with aging, though the work is preclinical.

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