TRPC channels are not required for graded persistent activity in entorhinal cortex neurons
Alexei V Egorov1, Dagmar Schumacher2, Rebekka Medert2
1Institute of Physiology and Pathophysiology, Heidelberg University, Heidelberg, Germany.
Canonical transient receptor potential (TRPC) channels do not mediate persistent firing in medial entorhinal cortex neurons. This finding rules out TRPC channels as the molecular identity of the calcium-activated nonselective cation current (ICAN) underlying this neuronal activity.
Area of Science:
- Neuroscience
- Molecular Biology
- Computational Neuroscience
Background:
- Adaptive behavior relies on short-term memory, often involving sustained neuronal firing.
- Persistent firing in medial entorhinal cortex (mEC) layer V (LV) neurons is linked to cholinergic muscarinic receptors and a calcium-activated nonselective cation current (ICAN).
Purpose of the Study:
- To investigate the molecular identity of the ICAN responsible for persistent firing in mEC LV neurons.
- To determine if canonical transient receptor potential (TRPC) channels are involved in muscarinic-dependent persistent neuronal activity.
Main Methods:
- Utilized two distinct lines of TRPC channel knockout mice: one lacking TRPC1, TRPC4, and TRPC5; the other lacking all seven TRPC family members.
- Recorded neuronal activity in layer V neurons of the medial entorhinal cortex in these knockout models.
Main Results:
- Persistent firing in mEC LV neurons was observed to be unchanged in TRPC channel-depleted mice.
- The absence of TRPC1, TRPC4, TRPC5, or all TRPC channels did not affect muscarinic-dependent persistent activity.
Conclusions:
- Canonical transient receptor potential (TRPC) channels are not essential for generating muscarinic-dependent persistent firing in mEC LV neurons.
- This study rules out TRPC channels as the molecular basis for the ICAN mediating this form of short-term memory crucial for adaptive behavior.
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