학술논문
The subcommissural organ regulates brain development via secreted peptides
Document Type
Original Paper
Author
Zhang, Tingting; Ai, Daosheng; Wei, Pingli; Xu, Ying; Bi, Zhanying; Ma, Fengfei; Li, Fengzhi; Chen, Xing-jun; Zhang, Zhaohuan; Zou, Xiaoxiao; Guo, Zongpei; Zhao, Yue; Li, Jun-Liszt; Ye, Meng; Feng, Ziyan; Zhang, Xinshuang; Zheng, Lijun; Yu, Jie; Li, Chunli; Tu, Tianqi; Zeng, Hongkui; Lei, Jianfeng; Zhang, Hongqi; Hong, Tao; Zhang, Li; Luo, Benyan; Li, Zhen; Xing, Chao; Jia, Chenxi; Li, Lingjun; Sun, Wenzhi; Ge, Woo-ping
Source
Nature Neuroscience. 27(6):1103-1115
Subject
Language
English
ISSN
1097-6256
1546-1726
1546-1726
Abstract
The subcommissural organ (SCO) is a gland located at the entrance of the aqueduct of Sylvius in the brain. It exists in species as distantly related as amphioxus and humans, but its function is largely unknown. Here, to explore its function, we compared transcriptomes of SCO and non-SCO brain regions and found three genes, Sspo, Car3 and Spdef, that are highly expressed in the SCO. Mouse strains expressing Cre recombinase from endogenous promoter/enhancer elements of these genes were used to genetically ablate SCO cells during embryonic development, resulting in severe hydrocephalus and defects in neuronal migration and development of neuronal axons and dendrites. Unbiased peptidomic analysis revealed enrichment of three SCO-derived peptides, namely, thymosin beta 4, thymosin beta 10 and NP24, and their reintroduction into SCO-ablated brain ventricles substantially rescued developmental defects. Together, these data identify a critical role for the SCO in brain development.
The subcommissural organ (SCO) is a gland in the brain, and relatively little is known about its function. Zhang et al. genetically ablated SCO cells and observed severe hydrocephalus and neuronal defects. The reintroduction of SCO-derived peptides into SCO-ablated brain substantially rescued developmental defects.
The subcommissural organ (SCO) is a gland in the brain, and relatively little is known about its function. Zhang et al. genetically ablated SCO cells and observed severe hydrocephalus and neuronal defects. The reintroduction of SCO-derived peptides into SCO-ablated brain substantially rescued developmental defects.