H2020Individual fellowship2020–2023

GABARPET · ImmunoPET directed to specific subtypes of GABAA receptors as strategy for molecular mapping of behaviour and mental illness

Horizon 2020 — Marie Skłodowska-Curie Actions

Duration
2020-09-09 → 2023-09-08
EU contribution
€304,021
Participants
1
Scheme
MSCA-IF

Lines connect the coordinator with its partners.

Results in brief

ImmunoPET directed to specific subtypes of GABAA receptors as strategy for molecular mapping of behaviour and mental illness

What is the problem/issue being addressed? The communication between neurons of the vertebrate’s brain is inhibited by an ion channel known as the GABA-A receptor. GABA-A receptors are formed by five proteins, or subunits, and their different classes are classified according to α subunit (α1–6). The differential expression of GABA-A receptors has been associated with schizophrenia or affective disorders between other pathologies or human conditions. In addition to the brain, GABA-A receptors have been detected in the peripheral nervous system of other organs such as the stomach, lungs, bladder, kidneys, liver and heart. Schizophrenia is a severe psychiatric disorder that has a profound effect on both the individuals affected and society. Postmortem investigations of GABA-A receptor α subunit expression have found reductions in α1 and increases in α2 expression, but inconsistent results for the α5 subunit. However, the density of GABA-A receptors in schizophrenia does not appear abnormal when it is studied in living patients though positron emission tomography (PET) in contrast to what the postmortem studies have demonstrated. Some researchers and GABARPET researchers believe that these negative findings can be explained because of the lack of PET tracers with high affinity and specificity. The immuno-positron emission tomography (immunoPET) is a non-invasive imaging technology based on tracking and quantification of radiolabeled monoclonal antibodies, antibody fragments, and peptides in vivo. Antibody imaging provides a specific and sensitive, noninvasive means for molecular detection of the cell surface proteins in vivo (e.g. ion channels), which aid diagnosis, prognosis, therapy selection, and monitoring of treatment for many diseases. Nevertheless, its success in neuroimaging is limited because intact antibodies cannot penetrate the Brain Blood Barrier (BBB) in healthy conditions. In 2019, a new type of bispecific antibody fragment, with one arm binding the neural target of interest and the other arm directed against the transferrin receptor expressed on the endothelial cells of BBB, was successfully created. This antibody fragment was able to cross the BBB, and it was used to visualize in vivo intrabrain amyloid-beta. Why is it important for society? Schizophrenia affects approximately 24 million people or 1 in 300 people (0.32%) worldwide. It is frequently associated with significant distress and impairment in personal, family, social, educational, occupational, and other important areas of life. The diagnosis of schizophrenia is clinical, made exclusively after obtaining a full psychiatric history and excluding other causes of psychosis. However, as other psychiatric disorders, schizophrenia no specific marker has been established thus far, and the development of antibody-based PET probes could help find them. Therefore, the high specificity of antibodies could be used to detect each of the 19 subunits of GABA-A receptors. In this way, new immunoPET tools could be developed to look for new biomarkers in neuropsychiatric disorders. In addition, this approach could be applied to other ion channels in the nervous system. In this research project, GABARPET researchers will utilize a completely novel approach to study the GABA-A receptor in the nervous system, which is expected to yield unprecedented insights into various diseases (e.g. Alzheimer's disease, epilepsy, schizophrenia, anxiety, etc.) and human conditions (Down syndrome, autism, etc..) in the future. What are the overall objectives? The goal of GABARPET researchers is to develop novel immunoPET radioligands capable of non-invasively detecting changes in GABA-A receptor subunits linked to neuropsychiatric disorders.

Data: CORDIS, © European Union

Project objective

Changes in GABA receptors are known hallmarks for numerous neurological diseases including schizophrenia which is a severe psychiatric disorder that has a profound effect on both the individuals affected and society. The diagnosis of schizophrenia is complex because of the loss of high specific biomarkers. Research papers have suggested that the differential expression of GABAA receptors in the brain is associated with this mental disease. The current evidence on GABAergic abnormalities in schizophrenia is mostly based on postmortem studies and, in this sense, in vivo measurements of GABAA receptor subunits can reveal additional insights. This project will develop Positron Emission Tomography (PET) probes which could unveil quantitative information about GABAA receptor expression in schizophrenia patients. However, the lack of imaging tracers with high affinity and specificity do not shed a clear light on the diagnosis in a traditional PET setting. In this sense, the immune-positron emission tomography (immunoPET) is a non-invasive technology based in antibody imaging which reveals a specific and sensitive molecular characterization of the cell surface phenotype in vivo. Nevertheless, its success in neuroimage is limited because of intact antibodies cannot penetrate the Brain Blood Barrier (BBB) in healthy conditions. However, GABARPET will tap into a small recombinant bispecific antibody construct targeting the GABAA receptors as well as the transferrin receptor because it is able to readily transmigrate across the BBB in vivo after peripheral injection.This project wants to develop di-single-chain variable fragment (di-scFv) directed to α1 and α2 subunits of GABAA receptors. Then, they will be labeled with conventional radionuclides produced by cyclotron as 18F and 89Zr. ImmunoPET probes will be used in wild-type mice, GABAA receptor knockout mice and different kind of rodent models of schizophrenia.

Original text from CORDIS.

Participants

  • TURUN YLIOPISTO · TurkuCoordinatorFinland

Links

Data: CORDIS, © European Union