A human-specific, concerted repression of microcephaly genes contributes to radiation-induced growth defects in cortical organoids.

 0 Người đánh giá. Xếp hạng trung bình 0

Tác giả: Sarah Baatout, Lisa Berden, Jasmine Buset, Winnok H De Vos, Emre Etlioglu, Ann Janssen, André Claude Mbouombouo Mfossa, Hanne Puype, Roel Quintens, Nicholas Rajan, Jessica Honorato Ribeiro, Vanessa Vermeirssen

Ngôn ngữ: eng

Ký hiệu phân loại:

Thông tin xuất bản: United States : iScience , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 210277

Prenatal radiation-induced DNA damage poses a significant threat to neurodevelopment, resulting in microcephaly which primarily affects the cerebral cortex. So far, mechanistic studies were done in rodents. Here, we leveraged human cortical organoids to model fetal corticogenesis. Organoids were X-irradiated with moderate or high doses at different time points. Irradiation caused a dose- and time-dependent reduction in organoid size, which was more prominent in younger organoids. This coincided with a delayed and attenuated DNA damage response (DDR) in older organoids. Besides the DDR, radiation induced premature differentiation of neural progenitor cells (NPCs). Our transcriptomic analysis demonstrated a concerted p53-E2F4/DREAM-dependent repression of primary microcephaly genes, which was independently confirmed in cultured human NPCs and neurons. This was a human-specific feature, as it was not observed in mouse embryonic brains or primary NPCs. Thus, human cortical organoids are an excellent model for DNA damage-induced microcephaly and to uncover potentially targetable human-specific pathways.
Tạo bộ sưu tập với mã QR

THƯ VIỆN - TRƯỜNG ĐẠI HỌC CÔNG NGHỆ TP.HCM

ĐT: (028) 36225755 | Email: tt.thuvien@hutech.edu.vn

Copyright @2024 THƯ VIỆN HUTECH