Neural precursor cells tune striatal connectivity through the release of IGFBPL1

Nat Commun. 2022 Dec 8;13(1):7579. doi: 10.1038/s41467-022-35341-y.

Abstract

The adult brain retains over life endogenous neural stem/precursor cells (eNPCs) within the subventricular zone (SVZ). Whether or not these cells exert physiological functions is still unclear. In the present work, we provide evidence that SVZ-eNPCs tune structural, electrophysiological, and behavioural aspects of striatal function via secretion of insulin-like growth factor binding protein-like 1 (IGFBPL1). In mice, selective ablation of SVZ-eNPCs or selective abrogation of IGFBPL1 determined an impairment of striatal medium spiny neuron morphology, a higher failure rate in GABAergic transmission mediated by fast-spiking interneurons, and striatum-related behavioural dysfunctions. We also found IGFBPL1 expression in the human SVZ, foetal and induced-pluripotent stem cell-derived NPCs. Finally, we found a significant correlation between SVZ damage, reduction of striatum volume, and impairment of information processing speed in neurological patients. Our results highlight the physiological role of adult SVZ-eNPCs in supporting cognitive functions by regulating striatal neuronal activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cardiac Electrophysiology
  • Humans
  • Insulin-Like Growth Factor Binding Proteins* / physiology
  • Lateral Ventricles* / physiology
  • Mice
  • Neural Stem Cells* / physiology
  • Tumor Suppressor Proteins* / physiology

Substances

  • IGFBPL1 protein, human
  • Insulin-Like Growth Factor Binding Proteins
  • Tumor Suppressor Proteins
  • IGFBPL-1 protein, mouse