RAC1 protein could be a new therapeutic target to fight neurodegeneration in Parkinsonʼs disease
A new research study reveals RAC1 protein could be a new therapeutic target to study the molecular mechanisms related to the neurodegenerative processes in Parkinsonʼs disease. The study, published in the online edition of the journal Molecular Neurobiology, is led by Antonella Consiglio, researcher at the Faculty of Medicine and Health Sciences of the University of Barcelona, the Institute of Biomedicine of the UB (IBUB) and the Bellvitge Biomedical Research Institute (IDIBELL), and Esther Dalfo, from the Univesitat Autònoma de Barcelona and Universitat de Vic - Universitat Central de Catalunya.
A new research study reveals RAC1 protein could be a new therapeutic target to study the molecular mechanisms related to the neurodegenerative processes in Parkinsonʼs disease. The study, published in the online edition of the journal Molecular Neurobiology, is led by Antonella Consiglio, researcher at the Faculty of Medicine and Health Sciences of the University of Barcelona, the Institute of Biomedicine of the UB (IBUB) and the Bellvitge Biomedical Research Institute (IDIBELL), and Esther Dalfo, from the Univesitat Autònoma de Barcelona and Universitat de Vic - Universitat Central de Catalunya.
The study describes new protection mechanisms to fight neurodegeneration which is common in neurodegenerative diseases -such as Parkinsonʼs and Alzheimerʼs-, which usually display a protein accumulation. The study shows that RAC1 protein -which takes part in the assembly of the active protein, one of the elements in the skeletal substance- could be an important regulatory factor in in Parkinsonʼs diseaseʼs neurodegeneration process.
From Caenorhabditis elegans model to patients suffering from Parkinson
In the first stages of the study, the experts proved there was a decrease in the activity of RAC1 protein in the Caenorhabditis elegans nematode -an animal model in biology and genomics- speeded up dopaminergic neuronal death and degeneration -the first ones affected by Parkinsonʼs disease. This process caused an accumulation of α-Synuclein, the main protein that piles up in several neurodegenerative diseases (Parkinsonʼs, Lewy body disease, etc.).
Moreover, the use of transcriptomics techniques -the study of RNA- in cells of patients with Parkinsonʼs showed that those genes that code proteins of the family of RAC1 were at lower levels compared to cells from those healthy individuals.
With these data, the scientific team studied a population of dopaminergic neurons from patients with Parkinsonʼs disease, which present a higher accumulation of α-Synuclein, a block in autophagy -the recycling machinery for cell compounds- and neuronal death.
Objective: boosting RAC1 proteinʼs function
These dopaminergic neurons, obtained from pluripotent cells from patientsʼ skin, “proved an increase of RAC1ʼs activity which produces an improvement in the markers of the previously described pathology”, says one of the first authors of the study, researcher Carles Catalayud, member of the IBUB, IDIBELL and the Center of Regenerative Medicine in Barcelona (CMRB). These results point out that boosting the function of RAC1 protein could balance the effects related to Parkinsonʼs disease, with a benefiting result for those patients.
Other experts take part in the study: Miguel Vila and Iria Carballo-Carbajal (University Hospital Vall dʼHebron, VHIR), Ángel Raya (CMRB-IDIBELL), José Miguel Lizcano (UAB), Antonio Miranda-Vizuete (University of Seville), Guy A. Caldwell, Kim A. Caldwell, Hannah Kim and Laura Berkozitz (University of Alabama, United States), among others.
The study has been funded by the Fondo de Investigación en Salud (Health Research Fund, FIS), the Ministry of Economy, Industry and Competitiveness (MINECO), Generalitat de Catalunya and the European Research Council (ERC).