Deciphering inhibitory neuron development: The paths to diversity

被引:9
作者
Bandler, Rachel C. [1 ,2 ]
Mayer, Christian [2 ]
机构
[1] Yale Univ, Dept Psychiat, New Haven, CT 06510 USA
[2] Max Planck Inst Biol Intelligence, D-82152 Martinsried, Germany
基金
欧洲研究理事会;
关键词
CAUDAL GANGLIONIC EMINENCE; FATE MAPPING REVEALS; CORTICAL INTERNEURON; ORIGINS; SPECIFICATION; EXPRESSION; FOREBRAIN; CELLS; NEUROGENESIS; MIGRATION;
D O I
10.1016/j.conb.2023.102691
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The regulation of fate decisions in progenitor cells lays the foundation for the generation of neuronal diversity and the formation of specialized circuits with remarkable processing capacity. Since the discovery more than 20 years ago that inhibitory (GABAergic) neurons originate from progenitors in the ventral part of the embryonic brain, numerous details about their development and function have been unveiled. GABAergic neurons are an extremely heterogeneous group, comprising many specialized subtypes of local interneurons and long-range projection neurons. Clearly distinguishable types emerge during postmitotic maturation, at a time when precursors migrate, morphologically mature, and establish synaptic con-nections. Yet, differentiation begins at an earlier stage within their progenitor domains, where a combination of birthdate and place of origin are key drivers. This review explains how new insights from single-cell sequencing inform our current under-standing of how GABAergic neuron diversity emerges.
引用
收藏
页数:8
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