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Key cellular auto-cleaning mechanism mediates formation of plaques in Alzheimer's brain

Date:
October 3, 2013
Source:
RIKEN
Summary:
Autophagy, a key cellular auto-cleaning mechanism, mediates the formation of amyloid beta plaques, one of the hallmarks of Alzheimer's disease. It might be a potential drug target for the treatment of the disease, concludes new research. The study sheds light on the metabolism of amyloid beta, and its role in neurodegeneration and memory loss.

Autophagy mediates Aβ secretion. wt and autophagy-deficient Atg7flox/flox; Nes-Cre primary neurons expressing APP were stained for Aβ.
Credit: Per Nilsson, RIKEN

Autophagy, a key cellular auto-cleaning mechanism, mediates the formation of amyloid beta plaques, one of the hallmarks of Alzheimer's disease. It might be a potential drug target for the treatment of the disease, concludes new research from the RIKEN Brain Science Institute in Japan. The study sheds light on the metabolism of amyloid beta, and its role in neurodegeneration and memory loss.

In a study published in the journal Cell Reports, Drs. Per Nilsson, Takaomi Saido and their team show for the first time using transgenic mice that a lack of autophagy in neurons prevents the secretion of amyloid beta and the formation of amyloid beta plaques in the brain. The study also reveals that an accumulation of amyloid beta inside neurons is toxic for the cells.

Alzheimer's disease, the most common form of dementia, affects nearly 36 million people worldwide, and this number is set to double over the next 20 years. However, the causes of the disease are not well understood and no disease-modifying treatment is available today.

Patients with Alzheimer's disease have elevated levels of the peptide amyloid beta in their brain and amyloid beta plaques form outside their neurons. This accumulation of amyloid beta causes the neurons to die, but until now the underlying mechanism remained a mystery. And whether the elevated levels of the peptide inside or outside the cells are to blame was unknown.

Autophagy is a cellular cleaning mechanism that normally clears any protein aggregates or other 'trash' within the cells, but that is somewhat disturbed in Alzheimer's patients.

To investigate the role of autophagy in amyloid beta metabolism, Nilsson et al. deleted an important gene for autophagy, Atg7, in a mouse model of Alzheimer's disease. Contrary to what they were expecting, their results showed that a complete lack of autophagy within neurons prevents the formation of amyloid beta plaque around/outside the cells. Instead, the peptide accumulates inside the neurons, where it causes neuronal death, which in turn leads to memory loss.

"Our study explains how amyloid beta is secreted from the neurons, via autophagy, which wasn't well understood," comments Dr Nilsson. "To control amyloid beta metabolism including its secretion is a key to control the disease. Autophagy might therefore be a potential drug target for the treatment of Alzheimer's disease," he adds.


Story Source:

The above story is based on materials provided by RIKEN. Note: Materials may be edited for content and length.


Journal Reference:

  1. Per Nilsson, Krishnapriya Loganathan, Misaki Sekiguchi, Yukio Matsuba, Kelvin Hui, Satoshi Tsubuki, Motomasa Tanaka, Nobuhisa Iwata, Takashi Saito, TakaomiC. Saido. Aβ Secretion and Plaque Formation Depend on Autophagy. Cell Reports, 2013; DOI: 10.1016/j.celrep.2013.08.042

Cite This Page:

RIKEN. "Key cellular auto-cleaning mechanism mediates formation of plaques in Alzheimer's brain." ScienceDaily. ScienceDaily, 3 October 2013. <www.sciencedaily.com/releases/2013/10/131003121254.htm>.
RIKEN. (2013, October 3). Key cellular auto-cleaning mechanism mediates formation of plaques in Alzheimer's brain. ScienceDaily. Retrieved September 30, 2014 from www.sciencedaily.com/releases/2013/10/131003121254.htm
RIKEN. "Key cellular auto-cleaning mechanism mediates formation of plaques in Alzheimer's brain." ScienceDaily. www.sciencedaily.com/releases/2013/10/131003121254.htm (accessed September 30, 2014).

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