The correct development of the brain cortex is an essential process for the acquisition of correct cognitive skills. Reelin, a key extracellular protein in neuronal migration and synaptic plasticity, is determinant in this process. For this reason, the dysfunction —genetic or at an expression level— of this protein is involved in neurodevelopmental pathologies —such as lissencephalies, epilepsy or some psychiatric disorders, particularly autism, schizophrenia and bipolar disorder— or neurodegenerative diseases.
Now, an article published in the journal Proceedings of the National Academy of Sciences (PNAS) reveals the decisive role of reelin expressed by the Cajal-Retzius pioneer neurons (CR) or cortical GABAergic neurons in the process of corticogenesis and neuronal migration. The study was led by Professor Eduardo Soriano, from the Department of Cell Biology, Physiology and Immunology of the Faculty of Biology and the Institute of Neurosciences (UBNeuro) of the University of Barcelona, and the Biomedical Research Networking Center on Neurodegenerative Diseases (CIBERNED), and its first authors are the researchers Alba Vílchez and Yasmina Manso (UB-UBNeuro-CIBERNED).
The study is based on the analysis of genetically modified mice to inactivate the reelin gene in pioneer CR neurons and cortical GABAergic interneurons. While CR cells play an essential role at early stages, “the study stresses the fundamental role of the GABAergic interneuron-derived reelin in late neuronal migration”, states Professor Eduardo Soriano.
A new model for reelin protein action
The team also described the existence of transient migratory deficits in some neuronal populations, a process that indicates that reelin expressed by any other of the neuronal populations is sufficient to reverse and compensate for some effects in cortical lamination in the brain. Based on this study, the authors present a new model of action for reelin, in the development of the cerebral cortex based on the cooperation and the spatial, cellular and sequential specific expression of this key protein.
Several neuropsychiatric disorders are linked to alterations in neuronal migration and reelin deficits in interneurons. “Thus, this study can provide a better understanding of the mechanisms associated with human brain disorders related to reelin deficits associated with migration alteration”, concludes the research team.
Among the coauthors of the study are Marta Pascual and Alba Elías-Tersa (UB-UBNeuro-CIBERNED); Víctor Borrell and Adrián Cárdenas, from the Institute of Neurosciences (CSIC-Miguel Hernández University); Manuel Álvarez-Dolado and Magdalena Martínez-Losa, from the Andalusian Center for Molecular Biology and Regenerative Medicine (CABIMER), and Angus C. Nairn, from Yale University (United States).
Proceedings of the National Academy of Sciences
Method of Research
Subject of Research
Specific contribution of Reelin expressed by Cajal–Retzius cells or GABAergic interneurons to cortical lamination
Article Publication Date