Modeling human neuronal migration deficits in 3D

Curr Opin Neurobiol. 2021 Feb:66:30-36. doi: 10.1016/j.conb.2020.09.005. Epub 2020 Oct 15.

Abstract

During the past few decades, we have witnessed an impressive gain in the knowledge regarding the basic mechanisms underlying human neuronal migration disorders by the usage of mouse models. Nevertheless, despite the remarkable conservation both in the genetic encoded information and the developmental processes, there are still numerous important differences between human and mouse. This may explain the vast excitement following the realization that technological breakthroughs enabled generating tissue-like human-based organoids for modeling human neuronal migration diseases. This review will provide a short introduction on human and mouse neuronal migration processes, and highlight human brain organoid models of neuronal migration diseases.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Animals
  • Cell Movement
  • Disease Models, Animal
  • Humans
  • Mice
  • Neurogenesis*
  • Neurons
  • Organoids*

Grants and funding