BCAT1 controls embryonic neural stem cells proliferation and differentiation in the upper layer neurons

• Published in: Molecular brain 2023-06, Vol.16 (1), p.53-53, Article 53
• Main Authors: Zhang, Shukui, Zhao, Jinyue, Zhao, Cheng, Su, Libo, Jiao, Jianwei
• Format: Article
• Language: English
• Subjects: Amino acids; Antibodies; BCAT1; Brain; Cell cycle; Cell differentiation; Cell Differentiation - genetics; Cell Proliferation; Cerebral cortex; Embryo cells; Glutamate; Glutamic Acid - metabolism; Laboratory animals; Neural progenitor cells; Neural stem cells; Neural Stem Cells - metabolism; Neurons; Neurons - metabolism; Quality control; Statistical analysis; Stem cells; Upper layer neurons
• ISSN: 1756-6606; 1756-6606
• DOI: 10.1186/s13041-023-01044-8

The regulation of neural stem cell (NSC) proliferation and differentiation during brain development is a precisely controlled process, with the production of different neuronal subtypes governed by strict timelines. Glutamate is predominantly used as a neurotransmitter by the subtypes of neurons in the various layers of the cerebral cortex. The expression pattern of BCAT1, a gene involved in glutamate metabolism, in the different layers of neurons has yet to be fully understood. Using single-cell data, we have identified seven different states of NSCs and found that state 4 is closely associated with the development of projection neurons. By inferring the developmental trajectory of different neuronal subtypes from NSC subsets of this state, we discovered that BCAT1 is involved in the regulation of NSC proliferation and differentiation and is specifically highly expressed in layer II/III and IV neurons. Suppression of BCAT1 through shRNA resulted in a reduction in NSC proliferation and an abnormal development of layer II/III and IV neurons. These findings provide new insights into the role of BCAT1 in the regulation of NSC behavior and neuronal development.