Persistent Lin28 Expression Impairs Neurite Outgrowth and Cognitive Function in the Developing Mouse Neocortex

Mol Neurobiol. 2019 May;56(5):3780-3795. doi: 10.1007/s12035-018-1297-0. Epub 2018 Sep 10.

Abstract

Many neurodevelopmental disorders feature learning and memory difficulties. Regulation of neurite outgrowth during development is critical for neural plasticity and memory function. Here, we show a novel regulator of neurite outgrowth during cortical neurogenesis, Lin28, which is an RNA-binding protein. Persistent Lin28 upregulation by in utero electroporation at E14.5 resulted in neurite underdevelopment during cortical neurogenesis. We also showed that Lin28-overexpressing cells had an attenuated response to excitatory inputs and altered membrane properties including higher input resistance, slower action potential repolarization, and smaller hyperpolarization-activated cation currents, supporting impaired neuronal functionality in Lin28-electroporated mice. When we ameliorated perturbed Lin28 expression by siRNA, Lin28-induced neurite underdevelopment was rescued with reduction of Lin28-downstream molecules, high mobility group AT-Hook 2, and insulin-like growth factor 1 receptor. Finally, Lin28-electroporated mice showed significant memory deficits as assessed by the Morris water maze test. Taken together, these findings demonstrate a new role and the essential requirement of Lin28 in developmental control of neurite outgrowth, which has an impact on synaptic plasticity and spatial memory. These findings suggest that targeting Lin28 may attenuate intellectual disabilities by correction of impaired dendritic complexity, providing a novel therapeutic candidate for treating neurodevelopmental disorders.

Keywords: Cognitive function; Cortical neurogenesis; Lin28; Neurite outgrowth; Neurodevelopmental disorders.

MeSH terms

  • Action Potentials
  • Animals
  • Cerebral Cortex / growth & development
  • Cognition / physiology*
  • Female
  • Gene Silencing
  • Green Fluorescent Proteins / metabolism
  • Lysine / analogs & derivatives
  • Lysine / metabolism
  • Mice, Inbred C57BL
  • Neocortex / metabolism*
  • Neurites / metabolism
  • Neurogenesis / genetics
  • Neuronal Outgrowth* / genetics
  • Phenotype
  • RNA, Small Interfering / metabolism
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / metabolism*
  • Synapses / physiology
  • Up-Regulation / genetics

Substances

  • Lin-28 protein, mouse
  • RNA, Small Interfering
  • RNA-Binding Proteins
  • Green Fluorescent Proteins
  • biocytin
  • Lysine