Treatment of epilepsy using a targeted p38γ kinase gene therapy.
Nicolle MoreyMagdalena PrzybylaJulia van der HovenYazi D KeFabien DelerueJanet van EerselLars M IttnerPublished in: Science advances (2022)
Hyperphosphorylated microtubule-associated protein tau has been implicated in dementia, epilepsy, and other neurological disorders. In contrast, site-specific phosphorylation of tau at threonine 205 (T205) by the kinase p38γ was shown to disengage tau from toxic pathways, serving a neuroprotective function in Alzheimer's disease. Using a viral-mediated gene delivery approach in different mouse models of epilepsy, we show that p38γ activity-enhancing treatment reduces seizure susceptibility, restores neuronal firing patterns, reduces behavioral deficits, and ameliorates epilepsy-induced deaths. Furthermore, we show that p38γ-mediated phosphorylation of tau at T205 is essential for this protection in epilepsy, as a lack of this critical interaction reinstates pathological features and accelerates epilepsy in vivo. Hence, our work provides a scope to harness p38γ as a future therapy applicable to acute neurological conditions.
Keyphrases
- protein kinase
- cerebrospinal fluid
- gene therapy
- temporal lobe epilepsy
- mouse model
- traumatic brain injury
- liver failure
- cerebral ischemia
- stem cells
- drug induced
- magnetic resonance
- magnetic resonance imaging
- tyrosine kinase
- sars cov
- drug delivery
- oxidative stress
- combination therapy
- cancer therapy
- cell therapy
- blood brain barrier
- hepatitis b virus
- respiratory failure
- stress induced