In a pair of new papers, researchers upend a long-held view about the basic functioning of a key receptor molecule involved in signaling between neurons.
And they describe how a compound linked to Alzheimer's disease impacts that receptor and weakens synaptic connections between brain cells The researchers are from the University of California, San Diego School of Medicine and the Royal Netherlands Academy of Arts and Sciences.
The findings are published in the Feb. 18 early edition of the Proceedings of the National Academy of Sciences.
"NMDA receptors are well known to allow the passage of calcium ions into cells and thereby trigger biochemical signaling," said principal investigator Roberto Malinow, MD, PhD professor of neurosciences at UC San Diego School of Medicine.
The new research, however, indicates that NMDA receptors can also operate independent of calcium ions. "It turns upside down a view held for decades regarding how NMDA receptors function," said Malinow, who holds the Shiley-Marcos Endowed Chair in Alzheimer's Disease Research in Honor of Dr. Leon Thal (a renowned UC San Diego Alzheimer's disease researcher who died in a single-engine airplane crash in 2007).
Specifically, Malinow and colleagues found that glutamate binding to the NMDA receptor caused conformational changes in the receptor that ultimately resulted in a weakened synapse and impaired brain function.
They also found that beta amyloid - a peptide that comprises the neuron-killing plaques associated with Alzheimer's disease - causes the NMDA receptor to undergo conformational changes that also lead to the weakening of synapses.
"These new findings overturn commonly held views regarding synapses and potentially identify new targets in the treatment of Alzheimer's disease," said Malinow.