Mice Study Implicates Brain Vessel Damage in Alzheimer’s
As published in Nature Communications, researchers used a mice model to show that blood vessel cells called pericytes may be a new target for treatment and diagnoses of Alzheimer’s disease.
“This study helps show how the brain’s vascular system may contribute to the development of Alzheimer’s disease,” said study leader Berislav V. Zlokovic, M.D. Ph.D.
Alzheimer’s disease is the leading cause of dementia. It is an age-related disease that gradually erodes a person’s memory, thinking and ability to perform everyday tasks.
Brains from Alzheimer’s patients typically have abnormally high levels of plaques made up of accumulations of beta-amyloid protein next to brain cells.
The protein clumps together to form neurofibrillary tangles inside neurons, and extensive neuron loss.
Vascular dementias, the second leading cause of dementia, are an assorted group of brain disorders caused by a range of blood vessel problems.
Brains from Alzheimer’s patients often show evidence of vascular disease, including ischemic stroke, small hemorrhages, and diffuse white matter disease, plus a buildup of beta-amyloid protein in vessel walls.
Moreover, previous studies have shown that a genetic risk factor for Alzheimer’s disease is linked to brain blood vessel health and integrity.
“This study may provide a better understanding of the overlap between Alzheimer’s disease and vascular dementia,” said Roderick Corriveau, Ph.D.
One hypothesis about Alzheimer’s disease states that increases in beta-amyloid lead to nerve cell damage in the brain.
This is supported by genetic studies that link familial forms of the disease to mutations in amyloid precursor protein (APP), the larger protein from which plaque-forming beta-amyloid molecules are derived.
Nonetheless, previous studies on mice showed that increased beta-amyloid levels reproduce some of the problems associated with Alzheimer’s.
The animals have memory problems, beta-amyloid plaques in the brain and vascular damage but none of the neurofibrillary tangles and neuron loss that are hallmarks of the disease.
In the current study, the researchers show that pericytes may be a key to whether increased beta-amyloid leads to tangles and neuron loss.
Pericytes are cells that surround the outside of blood vessels. Many are found in a kind of brain plumbing system called the blood-brain barrier.
The blood-brain barrier network fine-tunes the movement of cells and molecules between the blood and the interstitial fluid that surrounds the brain’s nerve cells.
Pericytes work with other blood-brain barrier cells to transport nutrients and waste molecules between the blood and the interstitial brain fluid.
To study how pericytes influence Alzheimer’s disease, Zlokovic and his colleagues crossbred mice genetically engineered to have a form of APP linked to familial Alzheimer’s with ones that have reduced levels of PDGFR-beta, a protein known to control pericyte growth and survival.
Previous studies showed that PDGFR-beta mutant mice have fewer pericytes than normal, decreased brain blood flow, and damage to the blood-brain barrier.
“Pericytes act like the gatekeepers of the blood-brain barrier,” said Zlokovic.
Both the APP and PDGFR-beta mutant mice had problems with learning and memory.
Crossbreeding the mice slightly enhanced these problems. The mice also had increased beta-amyloid plaque deposition near brain cells and along brain blood vessels.
Surprisingly, the brains of the crossbred mice had enhanced neuronal cell death and extensive neurofibrillary tangles in the hippocampus and cerebral cortex, regions that are typically affected during Alzheimer’s.
“Our results suggest that damage to the vascular system may be a critical step in the development of full-blown Alzheimer’s disease pathology,” said Zlokovic.
He and his colleagues concluded that their results support a two-hit vascular hypothesis of Alzheimer’s.
The hypothesis states that the toxic effects of increased beta-amyloid deposition on pericytes in aged blood vessels leads to a breakdown of the blood-brain barrier and a reduced ability to clear amyloid from the brain.
In turn, the progressive accumulation of beta-amyloid in the brain and death of pericytes may become a damaging feedback loop that causes dementia.
If true, then pericytes and other blood-brain barrier cells may be new therapeutic targets for treating Alzheimer’s disease.
Nauert PhD, R. (2015). Mice Study Implicates Brain Vessel Damage in Alzheimer’s. Psych Central. Retrieved on March 18, 2018, from https://psychcentral.com/news/2013/12/17/mice-study-implicates-brain-vessel-damage-in-alzheimers/63379.html