Chemogenetics, Induced Neurons and Pluripotent Stem Cells: Towards Advanced Gene and Cell Therapies Targeting Epilepsy

Natalia Avaliani

Research output: ThesisDoctoral Thesis (compilation)

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Abstract

The complexity of the central nervous system and existence of the blood-brain barrier often causes difficulties for traditional pharmacological treatments of neurological diseases. This thesis explores the feasibility and potential for novel gene and cell therapy approaches, which hold better promise for neurological disorders, while particularly targeting epilepsy.
Epilepsy is a multifactorial neurological disorder affecting 1% of the population. Available pharmacological therapies are merely symptomatic, and have severe side effects, while failing to adequately control seizures in one third of the patients, predominately in those with temporal lobe epilepsy (TLE). Targeted silencing of the pathological circuits by expressing therapeutic genes, or increasing the inhibition by introducing new populations of GABA-releasing neurons, might prove therapeutic for epilepsy, by counteracting seizures and even modifying the disease.
Gene therapy offers localized, cell-type specific alteration of neuronal excitability, but on-demand seizure suppression can only be achieved by tools allowing external temporal control. One such recently developed chemogenetic technology is based on viral expression of modified muscarinic G-protein coupled receptors, specifically activated by otherwise inert clozapine-N-oxide (CNO). In paper I, we explored if such modified receptor, hM4Di, which selectively activates Gi pathway, thereby causing neuronal inhibition, could suppress epileptiform activity upon CNO application. This approach proved effective for localized suppression of neuronal excitability and seizure-like events in an in vitro model of TLE, organotypic hippocampal slice cultures (OHSC), without altering intrinsic properties of the hM4Di-expressing neurons, demonstrating the therapeutic potential of this technology.
In papers II and III we characterized two different cell sources with the prospect of cell replacement therapy: induced Pluripotent Stem cells (iPS) and induced Neurons (iN). These two patient specific alternative cell sources offer a solution to ethical and immunogenicity issues, related to embryonic stem cell use.
Already six weeks after grafting in OHSCs, iPS-derived neuroepitelial-like stem cells (lt-NES), predominately differentiating to GABA-ergic neurons, displayed functional neuronal properties and certain rate of synaptic integration. In vivo studies showed that longer differentiation time (up to 24 weeks) was needed for the grafts to fully mature and extensively integrate into the host synaptic network. The grafted cells still retained some of the distinct electrophysiological features, however, such as high input resistance.
Next, we studied long-term survival of human foetal fibroblast-derived induced neurons (iN) in rodent hippocampus. Human iNs survive and maintain neuronal profile up to six months post-grafting, developing more elaborate neuronal morphology and complex dendritic arborisation over time. Graft-derived neurons with mature neuronal properties could be observed at six months, although a portion of non-converted fibroblasts, as well as asynchronous neuronal conversion was apparent among the grafts. Improvements in conversion, survival and integration rate of iN cells are required before these cells can offer a better alternative to iPS or stem cells. While showing potential as candidates for cell replacement therapy, both characterised cell types have to be further tested in relevant epilepsy model systems to demonstrate their therapeutic effect.
In summary, this thesis adds new knowledge and experimental basis for development of gene- and cell-based therapies for neurological disorders.
Original languageEnglish
QualificationDoctor
Awarding Institution
  • Epilepsy Center
Supervisors/Advisors
  • Kokaia, Merab, Supervisor
  • Andersson, My, Supervisor
Award date2015 Nov 6
Publisher
ISBN (Print)978-91-7619-197-2
Publication statusPublished - 2015

Bibliographical note

Defence details

Date: 2015-11-06
Time: 13:15
Place: A1005, Segerfalksalen, Wallenberg Neurocentrum, Sölvegatan 19, 223 62 Lund, Sweden

External reviewer(s)

Name: Silberberg, Gilad
Title: Associate Professor, PhD
Affiliation: Department of Neuroscience, Karolinska Institute, Stockholm, Sweden

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Subject classification (UKÄ)

  • Neurosciences

Keywords

  • Chemogenetics
  • iPS
  • iN
  • electrophysiology
  • gene and cell therapy
  • Epilepsy

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