News Release

Scripps Florida scientists shed new light on the role of calcium in learning and memory

Peer-Reviewed Publication

Scripps Research Institute

Ron Davis, Scripps Research Institute

image: Ron Davis is chair of the Department of Neuroscience at Scripps Florida. view more 

Credit: Photo courtesy of The Scripps Research Institute.

JUPITER, FL - August 25, 2016 - While calcium's importance for our bones and teeth is well known, its role in neurons--in particular, its effects on processes such as learning and memory--has been less well defined.

In a new study published in the journal Cell Reports, scientists from the Florida campus of The Scripps Research Institute (TSRI) offer new insights how calcium in mitochondria--the powerhouse of all cells--can impact the development of the brain and adult cognition.

In particular, the team showed in fruit flies, a widely used model system, that blocking a channel that brings calcium to the mitochondria, called "mitochondrial calcium uniporter," causes memory impairment but does not alter learning capacity.

"When we knocked down the activity of the uniporter, we found that flies have a deficit memory," said Ron Davis, chair of the TSRI's Department of Neuroscience. "Intact uniporter function is necessary for full and complete memory in the adult fly. What surprised us is that they were still able to learn--albeit with a fleeting memory. But we thought they wouldn't be able to learn at all."

The mitochondrial calcium uniporter protein, first identified in 2011, allows calcium ions to move from the cell's interior into mitochondria--like coal moving through a shoot into a furnace room. It is regulated by other proteins known as MICU1, MICU2 and EMRE. Davis noted that human patients with mutations in MICU1 can exhibit learning disabilities.

"The new study's conclusion is that mitochondrial calcium entry during development is necessary to establish the neuronal competency for supporting adult memory," said TSRI Research Associate Ilaria Drago, the first author of the study.

Drago noted the team found evidence that inhibiting mitochondrial calcium uniporter function led to a decrease in the content of synaptic vesicles (miniscule sacs within the cell where various neurotransmitters are stored) and an increase in the length of axons (the slender filaments of neurons).

While these structural problems were clearly observed, she added, what they mean in terms of neuronal development remains tantalizingly unclear. "The discovery of a developmental role for the mitochondrial calcium uniporter complex in regulating memory in adult flies is especially intriguing and deserves more exploration," said Davis.


The study, "Inhibiting the Mitochondrial Calcium Uniporter during Development Impairs Memory in Adult Drosophila," was supported by the National Institutes of Health (grants R37NS19904 and R01NS052351) and the Iris and Junming Le Foundation.

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