Abstract

For decades it has been hypothesized that molecules within the cerebrospinal fluid (CSF) diffuse into the brain parenchyma and influence the function of neurons. However, the functional consequences of CSF on neuronal circuits are largely unexplored and unknown. A major reason for this is the absence of appropriate neuronal in vitro model systems, and it is uncertain if neurons cultured in pure CSF survive and preserve electrophysiological functionality in vitro. In this article, we present an approach to address how human CSF (hCSF) influences neuronal circuits in vitro. We validate our approach by comparing the morphology, viability, and electrophysiological function of single neurons and at the network level in rat organotypic slice and primary neuronal cultures cultivated either in hCSF or in defined standard culture media. Our results demonstrate that rodent hippocampal slices and primary neurons cultured in hCSF maintain neuronal morphology and preserve synaptic transmission. Importantly, we show that hCSF increases neuronal viability and the number of electrophysiologically active neurons in comparison to the culture media. In summary, our data indicate that hCSF represents a physiological environment for neurons in vitro and a superior culture condition compared to the defined standard media. Moreover, this experimental approach paves the way to assess the functional consequences of CSF on neuronal circuits as well as suggesting a novel strategy for central nervous system (CNS) disease modeling.

Highlights

  • The interstitial fluid (ISF) of the brain parenchyma encompasses all brain cells, and thereby, represents the physiological environment of neurons in vivo

  • After the baseline neuronal activity in the human CSF (hCSF) and Hippocampal Neuronal Circuits In Vitro cultivation media was determined, we replaced the media with pure hCSF samples

  • Morphological examination did not reveal obvious differences between hippocampal neuronal cultures exposed to hCSF and fresh culture media for 3 days (Figure 2D). hCSF-treated hippocampal neuronal networks (n = 12, 8 hCSF obtained from different individuals were used and each sample were applied to 1–2 neuronal networks) showed a gradual increase in spiking activity in comparison to baseline activity (Figure 2)

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Summary

Introduction

The interstitial fluid (ISF) of the brain parenchyma encompasses all brain cells, and thereby, represents the physiological environment of neurons in vivo. Our current knowledge is based on electrophysiological characterization of neuronal circuits in acute hippocampal brain slices (Björefeldt et al, 2015), primary brain tissue (Otto et al, 2009) or mouse embryonic stem cell-derived neuronal cultures (Otto et al, 2009) exposed to human CSF (hCSF) for minutes or a few hours. By using multi-electrode array (MEA) recordings in neuronal cultures, we have shown that hCSF has an acute (

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