CRISPR Technique Identifies New Biomarker for Alzheimer's Disease

With the help of the CRISPR gene editing technique, a new biomarker for Alzheimer’s disease has been identified. The study reports that STIM1 protein deficiency could be associated with the uncommon version of the neurodegenerative disease. The findings of the study are published in the Journal of Molecular Medicine.

The objective of the research, undertaken in the laboratories of the IBPM, is to develop a model for studying Alzheimer's disease (AD) of sporadic origin, in other words, not due to a hereditary genetic mutation. While Alzheimer's disease of familial or hereditary type is responsible for around 5% of all cases, it is thought that 95% of its incidence is of unknown or sporadic origin.

‘STIM1 protein deficiency is seen in the brain tissue of Alzheimer's disease patients. Its involvement in neurodegenerative processes has been confirmed using CRISPR technique which may help identify the potential biomarker for Alzheimer's Disease.’
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"In Alzheimer's of family origin, there already exist animal models, because we know which genes are linked to this illness. However, in Alzheimer's disease of unknown origin, to date, there are no models that enable us to study how it develops", according to Francisco Javier Martin-Romero, one of the authors of the study.

These researchers analyzed cultures of damaged brain tissue from a region called Medial Frontal Gyrus, with clinically confirmed alterations provoked by Alzheimer. These clinical samples were analyzed and compared with healthy tissue from patients of the same age. As a result of this comparative study, the scientists found a deficiency in the protein STIM1 in brain tissue from patients with Alzheimer's disease.

"We have been working with this protein for ten years, but we weren't expecting these results with sporadic Alzheimer's," adds Martin-Romero. The next step the researchers took was to observe the involvement of this protein STIM1 in the neurodegeneration of the neuron, and they did so use the genetic editing system CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats), known as the "genetic cut-and-paste."

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The researchers applied a strategy to eliminate the expression of the gene STIM1 in the neuroblastoma SH-SY5Y cell line, editing the genome with CRISPR / Cas9, using an in vitro model to examine the phenotype of the neuronal cells deficient in STIM1.

"We use the CRISPR technique on a regular basis in the Faculty of Sciences at the UEx, as it has the great advantage that the genome remains stable despite the cuts in the DNA.

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In this specific case, the procedure CRISPR silences the gene which permits the expression of the protein STIM1 in the neuron. Thus, we were able to simulate what occurs in the neuron without this protein, and we observed alterations very similar to those seen in tissues with Alzheimer's", the researcher emphasizes.

Up to now, the effects of a deficiency in this protein critical to sporadic Alzheimer's were not known, and so this research gives us a new biomarker for the illness, in other words, an indicator of the progression of the neurodegenerative process.

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One of the alterations observed due to the deficiency of STIM1 is in the transport of calcium ions through the plasma membrane of the neurons.

"This calcium is necessary for the cell to be fully viable, and an alteration in this process affects its entire physiology, finally causing its death. The cell is unable to halt the transport of calcium, which becomes unregulated and out of control", states Martin-Romero.

The investigator highlights that this transport takes place through calcium ion channels regulated by a voltage. These voltage-gated calcium channels, the so-called L-type, can be blocked using pharmaceuticals based on dihydropyridine.

In fact, the team of researchers was able to halt cell death in vitro using pharmaceuticals based on dihydropyridine because of that blocking action, representing an important new finding in the treatment of Alzheimer's.

The next step for the investigators at the IBPM will be to work with pluripotent stem cells and differentiate them into neurons, firstly for mice and then for humans, to make the development of a model possible. This will allow a description of how the absence of stimulus or reduction in the protein STIM1 determines cell aging in sporadic Alzheimer's disease.

Source-Eurekalert