Author:
Suyama Kyoka,Adachi Toma,Mizuno Minami,Ji Kaiyuan,Isogai Eriko,Hasegawa Ikuko,Nishitani Kayo,Sone Masaki,Miyashita Satoshi,Owa Tomoo,Hoshino Mikio
Abstract
Astroglial cell diversity is essential for proper brain development and function in mammals. In mammalian cerebellum, three types of astroglial cells -Bergmann glial cells (BGs), inner granule cell layer (IGL) astrocytes, and white matter (WM) astrocytes- arise in postnatal timing from two types of progenitors: Bergmann glia-like progenitors (BGLPs) and astrocyte-like progenitors (AsLPs). While BGLPs are known to differentiate into BGs and IGL astrocytes in postnatal day 6 (P6) mice, their fate immediately after birth remains unclear due to technical challenges in specifically labeling BGLPs. In this study, we demonstrated that both BGLPs and AsLPs gradually decrease from P0 to P10. Using in vivo electroporation to label BGLPs, we found that BGLPs in P0 mice differentiate not only into BGs, IGL astrocytes but also WM astrocytes. Using spatial transcriptomics analysis (Xenium, 5k),we achieved the isolation and comparative profiling of BGLP clusters from P0 and P6 mice. This analysis revealed that P0 BGLPs exhibit more stem cell-like features, while P6 BGLPs show a shift toward BG-like characteristics. These findings indicate that BGLPs immediately after birth possess higher pluripotency than previously recognized.
Funder
JSPS KAKENHI
AMED
Intramural Research Grant of NCNP
Japan Health Research Promotion Bureau (JH) under Research Fund
Multilayered Stress Diseases
Tokumori Yasumoto Memorial Trust (MH) and Takeda Science Foundation
JST SPRING
Publisher
Cold Spring Harbor Laboratory