Ablation of Sphingosine 1-Phosphate Receptor Subtype 3 Impairs Hippocampal Neuron Excitability In vitro and Spatial Working Memory In vivo

• Published in: Frontiers in cellular neuroscience 2016-11, Vol.10, p.258-258
• Main Authors: Weth-Malsch, Daniela, Langeslag, Michiel, Beroukas, Dimitra, Zangrandi, Luca, Kastenberger, Iris, Quarta, Serena, Malsch, Philipp, Kalpachidou, Theodora, Schwarzer, Christoph, Proia, Richard L, Haberberger, Rainer V, Kress, Michaela
• Format: Article
• Language: English
• Subjects: Alzheimer's disease; Anxiety; Brain; Brain slice preparation; Central nervous system; Excitability; Experiments; Gene expression; Hippocampus; Kinases; Memory; mRNA; Multiple sclerosis; Neurodegenerative diseases; neuron excitability; Neurons; Neuroscience; Neurosciences; Physiology; Proteins; S1P Receptor 3; Short term memory; Spatial memory; Sphingosine 1-phosphate; Thermal cycling; working memory
• ISSN: 1662-5102; 1662-5102
• DOI: 10.3389/fncel.2016.00258

Understanding the role of the bioactive lipid mediator sphingosine 1-phosphate (S1P) within the central nervous system has recently gained more and more attention, as it has been connected to major diseases such as multiple sclerosis and Alzheimer's disease. Even though much data about the functions of the five S1P receptors has been collected for other organ systems, we still lack a complete understanding for their specific roles, in particular within the brain. Therefore, it was the aim of this study to further elucidate the role of S1P receptor subtype 3 (S1P ) and with a special focus on the hippocampus. Using an S1P knock-out mouse model we applied a range of behavioral tests, performed expression studies, and whole cell patch clamp recordings in acute hippocampal slices. We were able to show that S1P deficient mice display a significant spatial working memory deficit within the T-maze test, but not in anxiety related tests. Furthermore, mRNA was expressed throughout the hippocampal formation. Principal neurons in area CA3 lacking S1P showed significantly increased interspike intervals and a significantly decreased input resistance. Upon stimulation with S1P CA3 principal neurons from both wildtype and [Formula: see text] mice displayed significantly increased evoked EPSC amplitudes and decay times, whereas rise times remained unchanged. These results suggest a specific involvement of S1P for the establishment of spatial working memory and neuronal excitability within the hippocampus.