Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, Israel.
Department of biological sciences Tata Institute of Fundamental Research, Mumbai, India.
Curr Opin Neurobiol. 2021 Feb;66:30-36. doi: 10.1016/j.conb.2020.09.005. Epub 2020 Oct 15.
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.
在过去的几十年中,我们通过使用小鼠模型,见证了人类神经元迁移障碍的基础机制方面的知识取得了令人瞩目的进展。然而,尽管在遗传编码信息和发育过程方面都有显著的保守性,但人类和小鼠之间仍然存在许多重要的差异。这也许可以解释为什么当人们意识到技术突破使得能够生成类似于组织的基于人类的类器官来模拟人类神经元迁移疾病时,会引起如此巨大的兴奋。本文将简要介绍人类和小鼠的神经元迁移过程,并重点介绍神经元迁移疾病的人类脑类器官模型。