Identification and characterization of long non-coding RNA Carip in modulating spatial learning and memory

Cell Rep. 2022 Feb 22;38(8):110398. doi: 10.1016/j.celrep.2022.110398.

Abstract

CaMKII has long been known to be a key effector for synaptic plasticity. Recent studies have shown that a variety of modulators interact with the subunits of CaMKII to regulate the long-term potentiation (LTP) of hippocampal neurons. However, whether long non-coding RNAs modulate the activity of CaMKII and affect synaptic plasticity is still elusive. Here, we identify a previously uncharacterized long non-coding RNA Carip that functions as a scaffold, specifically interacts with CaMKIIβ, and regulates the phosphorylation of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) and N-methyl-d-aspartate (NMDA) receptor subunits in the hippocampus. The absence of Carip causes dysfunction of synaptic transmission and attenuates LTP in hippocampal CA3-CA1 synapses, which further leads to impairment of spatial learning and memory. In summary, our findings demonstrate that Carip modulates long-term synaptic plasticity by changing AMPA receptor and NMDA receptor activities, thereby affecting spatial learning and memory in mice.

Keywords: CaMKIIβ; Carip; LTP; hippocampal neurons; learning and memory.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2 / metabolism
  • High-Throughput Nucleotide Sequencing
  • Hippocampus / metabolism
  • Long-Term Potentiation / physiology
  • Mice
  • Neuronal Plasticity / physiology
  • RNA, Long Noncoding* / genetics
  • Receptors, AMPA / genetics
  • Receptors, AMPA / metabolism
  • Receptors, N-Methyl-D-Aspartate / genetics
  • Receptors, N-Methyl-D-Aspartate / metabolism
  • Spatial Learning*
  • Synapses / metabolism

Substances

  • RNA, Long Noncoding
  • Receptors, AMPA
  • Receptors, N-Methyl-D-Aspartate
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2