Institute of Physiology and Pathophysiology, Heidelberg University, Heidelberg, Germany.
Institute of Pharmacology, Heidelberg University, Heidelberg, Germany.
Hippocampus. 2019 Nov;29(11):1038-1048. doi: 10.1002/hipo.23094. Epub 2019 Apr 19.
Adaptive behavior requires the transient storage of information beyond the physical presence of external stimuli. This short-lasting form of memory involves sustained ("persistent") neuronal firing which may be generated by cell-autonomous biophysical properties of neurons or/and neural circuit dynamics. A number of studies from brain slices reports intrinsically generated persistent firing in cortical excitatory neurons following suprathreshold depolarization by intracellular current injection. In layer V (LV) neurons of the medial entorhinal cortex (mEC) persistent firing depends on the activation of cholinergic muscarinic receptors and is mediated by a calcium-activated nonselective cation current (I ). The molecular identity of this conductance remains, however, unknown. Recently, it has been suggested that the underlying ion channels belong to the canonical transient receptor potential (TRPC) channel family and include heterotetramers of TRPC1/5, TRPC1/4, and/or TRPC1/4/5 channels. While this suggestion was based on pharmacological experiments and on effects of TRP-interacting peptides, an unambiguous proof based on TRPC channel-depleted animals is pending. Here, we used two different lines of TRPC channel knockout mice, either lacking TRPC1-, TRPC4-, and TRPC5-containing channels or lacking all seven members of the TRPC family. We report unchanged persistent activity in mEC LV neurons in these animals, ruling out that muscarinic-dependent persistent activity depends on TRPC channels.
适应行为需要在外部刺激的物理存在之外短暂存储信息。这种短暂的记忆形式涉及持续(“持久”)的神经元放电,这可能是由神经元的自主生物物理特性或/和神经回路动力学产生的。许多来自脑切片的研究报告称,在细胞内电流注入超阈值去极化后,皮质兴奋性神经元中会产生内在产生的持久放电。在中内侧脑岛皮层(mEC)的 LV 神经元中,持久放电取决于乙酰胆碱能毒蕈碱受体的激活,并由钙激活的非选择性阳离子电流(I)介导。然而,这种电导率的分子身份仍然未知。最近,有人提出,潜在的离子通道属于经典的瞬时受体电位(TRPC)通道家族,包括 TRPC1/5、TRPC1/4 和/或 TRPC1/4/5 通道的异四聚体。虽然这一假设是基于药理学实验和 TRP 相互作用肽的作用,但基于 TRPC 通道耗尽动物的明确证据尚未得出。在这里,我们使用了两种不同的 TRPC 通道敲除小鼠品系,一种缺乏含有 TRPC1、TRPC4 和 TRPC5 的通道,另一种缺乏 TRPC 家族的所有七个成员。我们报告在这些动物中 mEC LV 神经元的持久活性没有改变,排除了依赖毒蕈碱的持久活性依赖于 TRPC 通道。