Abstract

Hypothalamic tanycytes are glial‐like glucosensitive cells that contact the cerebrospinal fluid of the third ventricle, and send processes into the hypothalamic nuclei that control food intake and body weight. The mechanism of tanycyte glucosensing remains undetermined. While tanycytes express the components associated with the glucosensing of the pancreatic β cell, they respond to nonmetabolisable glucose analogues via an ATP receptor‐dependent mechanism. Here, we show that tanycytes in rodents respond to non‐nutritive sweeteners known to be ligands of the sweet taste (Tas1r2/Tas1r3) receptor. The initial sweet tastant‐evoked response, which requires the presence of extracellular Ca2+, leads to release of ATP and a larger propagating Ca2+ response mediated by P2Y1 receptors. In Tas1r2 null mice the proportion of glucose nonresponsive tanycytes was greatly increased in these mice, but a subset of tanycytes retained an undiminished sensitivity to glucose. Our data demonstrate that the sweet taste receptor mediates glucosensing in about 60% of glucosensitive tanycytes while the remaining 40% of glucosensitive tanycytes use some other, as yet unknown mechanism.

Highlights

  • Hypothalamic tanycytes are a specialized type of glial cell found lining the third ventricle (Bolborea and Dale, 2013; Rodriguez, Blazquez, Pastor, Pelaez, Pena, Peruzzo, & Amat, 2005)

  • To explore the potential role of the sweet taste receptor in tanycyte signalling, we investigated three sweet-tasting compounds, which act as ligands for the sweet taste receptor: the artificial sweeteners sucralose and acesulfame K (AceK); and a natural sweetener derived from Stevia rebaudiana, rebaudioside A (RebA) (Li et al, 2002; Masuda et al, 2012; Sclafani, Bahrani, Zukerman, & Ackroff, 2010)

  • The three sweet tasting compounds induced repeatable responses in hypothalamic tanycytes that were larger than those evoked by control puffs of artificial CSF

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Summary

| INTRODUCTION

Hypothalamic tanycytes are a specialized type of glial cell found lining the third ventricle (Bolborea and Dale, 2013; Rodriguez, Blazquez, Pastor, Pelaez, Pena, Peruzzo, & Amat, 2005). The increase of Ca21 inside the tanycytes may through an unknown mechanism, lead to release of ATP from the tanycyte, which may feed back onto the original activated cell leading to release of Ca21 from intracellular stores, or stimulate neighboring cells propagating the Ca21 wave (Bolborea and Dale, 2013; Frayling et al, 2011). While this is a possible explanation, the mechanism involved is rather complex.

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| RESULTS
| DISCUSSION
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