An AKT3-FOXG1-reelin network underlies defective migration in human focal malformations of cortical development

Seung Tae Baek, Brett Copeland, Eun Jin Yun, Seok Kyu Kwon, Alicia Guemez-Gamboa, Ashleigh E. Schaffer, Sangwoo Kim, Hoon Chul Kang, Saera Song, Gary W. Mathern, Joseph G. Gleeson

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79 Citations (Scopus)


Focal malformations of cortical development (FMCDs) account for the majority of drug-resistant pediatric epilepsy. Postzygotic somatic mutations activating the phosphatidylinositol-4,5-bisphosphate-3-kinase (PI3K)-protein kinase B (AKT)-mammalian target of rapamycin (mTOR) pathway are found in a wide range of brain diseases, including FMCDs. It remains unclear how a mutation in a small fraction of cells disrupts the architecture of the entire hemisphere. Within human FMCD-affected brain, we found that cells showing activation of the PI3K-AKT-mTOR pathway were enriched for the AKT3E17K mutation. Introducing the FMCD-causing mutation into mouse brain resulted in electrographic seizures and impaired hemispheric architecture. Mutation-expressing neural progenitors showed misexpression of reelin, which led to a non-cell autonomous migration defect in neighboring cells, due at least in part to derepression of reelin transcription in a manner dependent on the forkhead box (FOX) transcription factor FOXG1. Treatments aimed at either blocking downstream AKT signaling or inactivating reelin restored migration. These findings suggest a central AKT-FOXG1-reelin signaling pathway in FMCD and support pathway inhibitors as potential treatments or therapies for some forms of focal epilepsy.

Original languageEnglish
Pages (from-to)1445-1454
Number of pages10
JournalNature Medicine
Issue number12
Publication statusPublished - 2015 Dec 1

Bibliographical note

Funding Information:
We thank N. Cai, M. Huynh, T. Chirwa, K. Um, J. Silhavy and U. Yang for technical expertise. This work was supported by the US National Institutes of Health (grant no. R01NS083823; J.G.G. and G.W.M.), the Simons Foundation for Autism Research (grant no. 275275; J.G.G.), the Howard Hughes Medical Institute (J.G.G.), the 2014 National Alliance for Research on Schizophrenia and Depression (NARSAD) Young Investigator Grant from the Brain & Behavior Research Foundation (grant no. 22892; S.T.B.), a Human Frontier Science Program Long-Term Fellowship (S.-K.K.), an A.P. Giannini Foundation Fellowship (A.E.S.) and an NIH NICHD K99/R00 Pathway to Independence Award (grant no. K99HD082337; A.E.S.). G.W.M. was supported by the Dr. Alfonsina Q. Davies Endowed Chair in honor of Paul Crandall MD for Epilepsy Research. We thank the UCSD Neuroscience Microscopy Core P30 NS047101 for imaging support, K. Jepsen from the UCSD Institute for Genomic Medicine Core Facility, the UCSD Human Embryonic Stem Cell Core Facility, A. Roberts from the Scripps Research Institute Animal Core Facility, I. Verma (Salk Institute) for the pBOB-Switch vector, A. Acharya (University of Texas Southwestern Medical Center) for the Cre-expressing adenovirus, G. Fishell (New York University) for the Foxg1 plasmid, and P. Mischel, I. Martin-Valencia, T. Curran and T. Park for discussions.

Publisher Copyright:
© 2015 Nature America, Inc. All rights reserved.

All Science Journal Classification (ASJC) codes

  • Biochemistry, Genetics and Molecular Biology(all)


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