Abstract

BackgroundThe present work was performed to investigate the ability of two different embryonic stem (ES) cell-derived neural precursor populations to generate functional neuronal networks in vitro. The first ES cell-derived neural precursor population was cultivated as free-floating neural aggregates which are known to form a developmental niche comprising different types of neural cells, including neural precursor cells (NPCs), progenitor cells and even further matured cells. This niche provides by itself a variety of different growth factors and extracellular matrix proteins that influence the proliferation and differentiation of neural precursor and progenitor cells. The second population was cultivated adherently in monolayer cultures to control most stringently the extracellular environment. This population comprises highly homogeneous NPCs which are supposed to represent an attractive way to provide well-defined neuronal progeny. However, the ability of these different ES cell-derived immature neural cell populations to generate functional neuronal networks has not been assessed so far.ResultsWhile both precursor populations were shown to differentiate into sufficient quantities of mature NeuN+ neurons that also express GABA or vesicular-glutamate-transporter-2 (vGlut2), only aggregate-derived neuronal populations exhibited a synchronously oscillating network activity 2-4 weeks after initiating the differentiation as detected by the microelectrode array technology. Neurons derived from homogeneous NPCs within monolayer cultures did merely show uncorrelated spiking activity even when differentiated for up to 12 weeks. We demonstrated that these neurons exhibited sparsely ramified neurites and an embryonic vGlut2 distribution suggesting an inhibited terminal neuronal maturation. In comparison, neurons derived from heterogeneous populations within neural aggregates appeared as fully mature with a dense neurite network and punctuated vGlut2 expression within presynaptic vesicles. Also those NPCs that had migrated away from adherent neural aggregates maintained their ability to generate a synchronously oscillating neuronal network, even if they were separated from adherent aggregates, dissociated and re-plated.ConclusionThese findings suggest that the complex environment within niches and aggregates of heterogeneous neural cell populations support the generation of fully mature neurons and functional neuronal networks from ES cell-derived neural cells. In contrast, homogeneous ES cell-derived NPCs within monolayer cultures exhibited an impaired functional neuronal maturation.

Highlights

  • The present work was performed to investigate the ability of two different embryonic stem (ES) cell-derived neural precursor populations to generate functional neuronal networks in vitro

  • These findings suggest that the complex environment within niches and aggregates of heterogeneous neural cell populations support the generation of fully mature neurons and functional neuronal networks from ES cell-derived neural cells

  • SFEBs were cultivated as free-floating aggregates in neural proliferation medium (NPM) under the influence of epidermal growth factor (EGF) and fibroblast growth factor-2 (FGF-2) and passaged at least 23 times whereupon neural precursor cell-enriched SFEBs had developed

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Summary

Introduction

The present work was performed to investigate the ability of two different embryonic stem (ES) cell-derived neural precursor populations to generate functional neuronal networks in vitro. Functional biological neuronal networks in vitro can be derived from primary tissue-derived neurons and represent populations of synaptically interconnected cells capable of generating synchronous electrophysiological activity [1,2,3,4,5,6]. In vitro generated neuronal networks that represent the basic principle for brain activity can be used to analyze the electrophysiological development and quality of interconnected neuronal populations of different cell sources as well as their reactions to pharmacologically active compounds. The rationale for using ES cell-derived instead of primary tissue-derived neural populations is the increased homogeneity and controllability of in vitro generated functional neuronal networks whose reactions, for instance, to different pharmacological compounds strongly depend on the standardization of the cell culture. The possibility of measuring the electrophysiological function of in vitro generated neuronal networks permits to verify the quality of different precursor-derived neuronal populations prior to transplantation within the scope of regenerative medicine

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