4.7 Article

Ablation of glucokinase-expressing tanycytes impacts energy balance and increases adiposity in mice

Journal

MOLECULAR METABOLISM
Volume 53, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.molmet.2021.101311

Keywords

Glucokinase; Tanycytes; Energy balance; Glucose homeostasis; Apoptosis; Hypothalamus

Funding

  1. Swiss National Science Foundation [PZ00P3_174120, PCEFP3_194551, 310030_185292, 310030-182496]
  2. European Research Council Starting Grant (TANGO) [948196]
  3. Novartis Foundation for medical-biological research
  4. Horizon2020 [847941]
  5. Novartis Foun-dation [18A052]
  6. European Research Council Advanced Grant (INTEGRATE) [694798]
  7. Swiss National Science Foundation (SNF) [PCEFP3_194551, PZ00P3_174120, 310030_185292] Funding Source: Swiss National Science Foundation (SNF)
  8. European Research Council (ERC) [948196, 694798] Funding Source: European Research Council (ERC)

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This study investigated the role of GCK-expressing tanycytes in the regulation of energy balance in mice. The results showed that Gck deletion induced the death of tanycytes and affected adiposity in mice, as well as NPY neuron function.
Objectives: Glucokinase (GCK) is critical for glucosensing. In rats, GCK is expressed in hypothalamic tanycytes and appears to play an essential role in feeding behavior. In this study, we investigated the distribution of GCK-expressing tanycytes in mice and their role in the regulation of energy balance. Methods: In situ hybridization, reporter gene assay, and immunohistochemistry were used to assess GCK expression along the third ventricle in mice. To evaluate the impact of GCK-expressing tanycytes on arcuate neuron function and mouse physiology, Gck deletion along the ventricle was achieved using loxP/Cre recombinase technology in adult mice. Results: GCK expression was low along the third ventricle, but detectable in tanycytes facing the ventromedial arcuate nucleus from bregma -1.5 to -2.2. Gck deletion induced the death of this tanycyte subgroup through the activation of the BAD signaling pathway. The ablation of GCK-expressing tanycytes affected different aspects of energy balance, leading to an increase in adiposity in mice. This phenotype was systematically associated with a defect in NPY neuron function. In contrast, the regulation of glucose homeostasis was mostly preserved, except for glucoprivic responses. Conclusions: This study describes the role of GCK in tanycyte biology and highlights the impact of tanycyte loss on the regulation of energy balance. (C) 2021 The Author(s). Published by Elsevier GmbH.

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