Univ. Lille, Inserm, CHU Lille, Laboratory of Development and Plasticity of the Neuroendocrine Brain, Lille Neuroscience & Cognition, UMR-S1172, 59000 Lille, France.
STAR Protoc. 2023 Dec 15;4(4):102571. doi: 10.1016/j.xpro.2023.102571. Epub 2023 Sep 21.
Here, we present a protocol for tanycyte-neuron paired whole-cell patch-clamp recording in living mouse brain slices. We describe steps for mice generation, solution preparation, and dissection. We then detail realization of slices and patch-clamp recordings. While we use, as an example, tanycytes of the arcuate nucleus of the hypothalamus and pro-opiomelanocortin neurons, this protocol can be adapted to study metabolic coupling between tanycytes and any neuronal population. For complete details on the use and execution of this protocol, please refer to Lhomme et al. (2021)..
在这里,我们提供了一个在活体小鼠脑切片中进行 tanycyte-神经元配对全细胞膜片钳记录的方案。我们描述了小鼠的生成、溶液的制备和解剖步骤。然后,我们详细介绍了切片和膜片钳记录的实现。虽然我们以下丘脑弓状核的 tanycytes 和 pro-opiomelanocortin 神经元为例,但该方案可以适应研究 tanycytes 与任何神经元群体之间的代谢偶联。如需了解此方案的使用和执行的完整详细信息,请参考 Lhomme 等人。(2021)。