The AMG pathway is established as a mechanistic framework for identifying digenic etiologies in epilepsy and highlight potential therapeutic targets after it was demonstrated that reduced actin polymerization promoted DRP1-mediated mitochondrial fission, increased ROS levels, and enhanced glutamatergic transmission, leading to seizures.
Abstract
Epilepsy affects approximately 50 million people worldwide, yet more than half of individuals with a presumed genetic cause still lack a molecular diagnosis despite the identification of over 1,000 monogenic epilepsy genes. This diagnostic gap is unlikely to be resolved by improved variant detection alone, suggesting that variants affecting the same biological pathway may combine to cause disease. By studying epilepsy-associated actin regulatory genes, we identified a conserved actin/mitochondria/glutamate (AMG) pathway. We demonstrate that reduced actin polymerization promoted DRP1-mediated mitochondrial fission, increased ROS levels, and enhanced glutamatergic transmission, leading to seizures. The glial innate immune pathway, a recently recognized contributor to epilepsy, is activated when the AMG pathway is affected. Reducing mitochondrial fission with the mitochondria division inhibitor (Mdivi-1), or suppressing ROS with N-acetyl-l-cysteine amide (NACA), significantly alleviated seizures. Importantly, digenic heterozygous loss-of-function variants in AMG pathway genes combined to cause seizures, and individuals with epilepsy of unknown etiology showed an increased burden of such variants when compared with the controls. Modeling patient-specific digenic combinations in Drosophila confirmed that many combinations promote seizure susceptibility. Together, these findings establish the AMG pathway as a mechanistic framework for identifying digenic etiologies in epilepsy and highlight potential therapeutic targets.
It is shown that overexpression of patient variants leads to protein degradation and dysregulation of microtubule acetylation in cultured HEK cells, and this data suggest that CAMSAP3 plays an important role in genetic generalized epilepsy.
C. M. LaCoursiere, Zachary Stayn, Hannah Hepner et al.· bioRxiv· 0 citations
The existing literature on astrocyte dysfunction in genetic epilepsy syndromes and neurodevelopmental disorders with seizures is reviewed and several key studies that highlight alterations in crucial astrocyte functions including calcium signaling and ion homeostasis are identified.
Jenny Lange, Eric Zhao, Ellie O'Connell et al.· Journal of Neuroscience Rese...· 0 citations
This review synthesizes contemporary insights into the genetic and molecular pathophysiology of seizures and epilepsy, with emphasis on mechanisms that destabilize excitation–inhibition balance, promote epileptogenesis, and drive pharmacoresistance and supports more refined approaches to epilepsy classification and fut...
Mohammad Reza Seyedtaghia, Jina Babanzadeh, M. Scala et al.· Epilepsia Open· 0 citations
The use of an adenine base editor (ABE) to directly correct SCN1AR613X, a recurrent variant found in patients with DS, suggests the therapeutic potential of prime editing for the treatment of patients with SCN1A-associated GEFS+.
Samantha A Dow, Tracy A. Bedrosian· Epilepsy Currents· 0 citations
A post-mortem investigation of post-mortem brain tissues from 12 patients with POLG-related mitochondrial epilepsy provides strong neuropathological evidence implicating neuroinflammation and glial dysfunction in POLG-related epilepsy.
Laura A. Smith, Megan Wilson, Elsaid Mohamed Elsaid et al.· bioRxiv· 0 citations
This study demonstrates that FLX provides neuroprotective and cognitive benefits in murine epilepsy models by inhibiting neuronal ferroptosis, highlighting its therapeutic potential for epilepsy and other ferroptosis-related neurological disorders.
Yu-Xiang Li, Cong Wang, Meng-Ying Huang et al.· Journal of Advanced Research· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.