AUTHOR=Pancho Anna , Mitsogiannis Manuela D. , Aerts Tania , Dalla Vecchia Marco , Ebert Lena K. , Geenen Lieve , Noterdaeme Lut , Vanlaer Ria , Stulens Anne , Hulpiau Paco , Staes Katrien , Van Roy Frans , Dedecker Peter , Schermer Bernhard , Seuntjens Eve TITLE=Modifying PCDH19 levels affects cortical interneuron migration JOURNAL=Frontiers in Neuroscience VOLUME=16 YEAR=2022 URL=https://www.frontiersin.org/journals/neuroscience/articles/10.3389/fnins.2022.887478 DOI=10.3389/fnins.2022.887478 ISSN=1662-453X ABSTRACT=
PCDH19 is a transmembrane protein and member of the protocadherin family. It is encoded by the X-chromosome and more than 200 mutations have been linked to the neurodevelopmental PCDH-clustering epilepsy (PCDH19-CE) syndrome. A disturbed cell-cell contact that arises when random X-inactivation creates mosaic absence of PCDH19 has been proposed to cause the syndrome. Several studies have shown roles for PCDH19 in neuronal proliferation, migration, and synapse function, yet most of them have focused on cortical and hippocampal neurons. As epilepsy can also be caused by impaired interneuron migration, we studied the role of PCDH19 in cortical interneurons during embryogenesis. We show that cortical interneuron migration is affected by altering PCDH19 dosage by means of overexpression in brain slices and medial ganglionic eminence (MGE) explants. We also detect subtle defects when PCDH19 expression was reduced in MGE explants, suggesting that the dosage of PCDH19 is important for proper interneuron migration. We confirm this finding