Protein Changes Linked to Symptoms of Alzheimer's Disease
News Aug 15, 2013
Cavener and his colleagues were hunting deep in the brain's molecular machinery to discover what was going wrong there that causes the brains of patients with Alzheimer's Disease to lose the ability to make sufficient proteins. The continual production of fresh proteins is an essential process in the brain that is necessary for learning and the long-term storage of memories.
A clue from a recent discovery showed that something was suspiciously wrong with a particular protein. This protein, called PERK, is essential for regulating protein synthesis to be at just the right level for normal brain functions. Using the brains of humans with Alzheimer's Disease and also special "AD" mice used in research labs to model the disease in mammals, researchers had found that PERK was overactive and consequently was misregulating the synthesis of proteins.
"To determine if PERK overactivity was related to the symptoms of Alzheimer's disease, we developed in our lab at Penn State a genetic mutation of PERK in the brains of a strain of laboratory mice," Cavener said. Eric Klann's laboratory at New York University, in collaboration with Cavener's lab at Penn State, then studied how the loss of PERK in the brain influenced Alzheimer's Disease symptoms. "Our research team found that removal of PERK from an AD mouse actually reduced AD symptoms," Cavener said. "The learning and memory functions, which are severely impaired in AD mice, now were substantially improved when PERK was removed from the brain." In addition, the scientists found that, within the brain, removal of PERK in AD mice also led to predicted improvement in the regulation of protein synthesis.
"Our studies suggest that reducing PERK activity in the brain of Alzheimer's Disease patients may offer a new therapy for Alzheimer's Disease" Cavener said. "However, such therapy would have to be specifically targeted at the brain because loss of PERK in other parts of the body, including the pancreas, can quickly lead to diabetes."
Restoring the ability to walk following spinal cord injury requires neurons in the brain to reestablish communication pathways with neurons in the spinal cord, Mature neurons, however, are unable to regenerate their axons to facilitate this process. New research in mice shows one potential route to overcome this limitation may be by targeting liver kinase B1 (LKB1) protein.
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