Neuronal Menin Overexpression Rescues Learning and Memory Phenotype in CA1-Specific α7 nAChRs KD Mice

Cells. 2021 Nov 24;10(12):3286. doi: 10.3390/cells10123286.

Abstract

The perturbation of nicotinic cholinergic receptors is thought to underlie many neurodegenerative and neuropsychiatric disorders, such as Alzheimer's and schizophrenia. We previously identified that the tumor suppressor gene, MEN1, regulates both the expression and synaptic targeting of α7 nAChRs in the mouse hippocampal neurons in vitro. Here we sought to determine whether the α7 nAChRs gene expression reciprocally regulates the expression of menin, the protein encoded by the MEN1 gene, and if this interplay impacts learning and memory. We demonstrate here that α7 nAChRs knockdown (KD) both in in vitro and in vivo, initially upregulated and then subsequently downregulated menin expression. Exogenous expression of menin using an AAV transduction approach rescued α7 nAChRs KD mediated functional and behavioral deficits specifically in hippocampal (CA1) neurons. These effects involved the modulation of the α7 nAChR subunit expression and functional clustering at the synaptic sites. Our data thus demonstrates a novel and important interplay between the MEN1 gene and the α7 nAChRs in regulating hippocampal-dependent learning and memory.

Keywords: brain connectivity; extracellular activity; learning and memory; menin; nicotinic cholinergic receptors; synaptogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bungarotoxins / metabolism
  • CA1 Region, Hippocampal / metabolism*
  • Disks Large Homolog 4 Protein / metabolism
  • Female
  • Gene Expression Regulation
  • Memory*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Neurogenesis
  • Neurons / metabolism*
  • Organ Specificity
  • Phenotype
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism*
  • Synapses / metabolism
  • Synaptotagmin I / metabolism
  • alpha7 Nicotinic Acetylcholine Receptor / metabolism*

Substances

  • Bungarotoxins
  • Disks Large Homolog 4 Protein
  • Dlg4 protein, mouse
  • Men1 protein, mouse
  • Proto-Oncogene Proteins
  • Synaptotagmin I
  • Syt1 protein, mouse
  • alpha7 Nicotinic Acetylcholine Receptor

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