Unravelling potential mechanisms causing astrocytic death during early epileptogensis
1 Institute of Cellular Neuroscience, Medical Faculty, University of Bonn
Epilepsy is a disorder of the brain characterised by unprovoked, recurrent seizures and affects about 1% of the population worldwide. A deeper understanding of the cellular mechanisms leading to epilepsy is essential for the identification of novel targets for therapeutic intervention. Growing evidence suggests that dysfunctional astrocytes are crucial players in the development of temporal lobe epilepsy (TLE). In a mouse model of TLE with hippocampal sclerosis (HS) we found a transient but significant reduction in the number of GFAP-positive astrocytes in the CA1 stratum radiatum (SR) of the ipsilateral hippocampus, starting 4 hours after kainate-induced status epilepticus (SE). Xpro1959, a soluble TNFɑ antagonist, largely mitigated the decrease of astrocyte number. At 3 days after SE induction, astrocyte cell numbers recovered to the initial values, which was accompanied by enhanced proliferation. The goal of the present study was to elucidate molecular mechanism(s) causing astrocytic loss. We used immunohistochemical staining and semiquantitative RT-PCR analysis to identify markers of cell death mechanisms, 4 hours after epilepsy induction. We did not find any cleaved-caspase 3 or TUNEL positive astrocytes in the epileptic tissue, ruling out the involvement of apoptotic death. A contribution of autophagic cell death could also be excluded since we observed only low/negligible expression of autophagy-related genes and proteins (lc3a, lamp2, becn1, LC3B). However, we found a significant increase of receptor interacting protein kinase 3 (RIPK3)- and mixed lineage kinase domain-like protein (MLKL)-positive astrocytes, as well as enhanced expression of the corresponding necroptosis-related genes (ripk3 and mlkl) in the ipsilateral CA1 SR of kainate-injected mice. Moreover, using phospho-specific antibodies ipsilaterally we observed phosphorylation of MLKL (pMLKL) and the formation of necrosome complexes between RIPK3 and pMLKL in kainate-injected animals. Co-localization analysis showed translocation of pMLKL to the nucleus and the plasma membrane in astrocytes of the ipsilateral hippocampus. Taken together, the present study suggests that a considerable proportion of hippocampal astrocytes undergo necroptotic cell death during early epileptogenesis.