Purkinje cell arrival at the Purkinje cell layer orchestrates cerebellar foliation and its temporal sequence

Cerebellar foliation proceeds in a stereotyped manner, but the developmental mechanisms that regulate its temporal sequence remain unclear. In reeler and yotari , abnormal Purkinje cell (PC) positioning and foliation defects coexist, yet their causal relationship remains unsolved. Here, using temporally controlled, PC-specific deletion of DAB1, we examined how PC migration relates to foliation. We show that postnatal DAB1 loss disrupts PC positioning and foliation in lobules VI/VII, and that even mild PC displacement from the PC layer (PCL) reduces local proliferation of granule cell precursors (GCPs), while Sonic hedgehog (SHH) supplementation rescues these foliation defects. Furthermore, we find that PC arrival at the PCL differs across lobules, accompanied by lobule-specific peaks in GCP proliferation. These findings identify PC arrival at the PCL as a developmental process that enables effective SHH signaling, thereby promoting foliation, and indicate that spatial differences in PC arrival timing orchestrate the temporal sequence of cerebellar foliation.

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Publication Details

Journal
iScience
Published
2026-09-01
DOI
https://doi.org/10.1016/j.isci.2026.116664
Primary Topic
Neurogenesis and neuroplasticity mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

Purkinje cell arrival at the Purkinje cell layer orchestrates cerebellar foliation and its temporal sequence

Ryosuke Uchi, Kazunori Nakajima, Yuki Hirota, Takao Honda et al.
iScience
Neurogenesis and neuroplasticity mechanisms
article

Purkinje cell arrival at the Purkinje cell layer orchestrates cerebellar foliation and its temporal sequence

Ryosuke Uchi, Kazunori Nakajima, Yuki Hirota, Takao Honda, Takuto Kasai
article en

Abstract

Cerebellar foliation proceeds in a stereotyped manner, but the developmental mechanisms that regulate its temporal sequence remain unclear. In reeler and yotari , abnormal Purkinje cell (PC) positioning and foliation defects coexist, yet their causal relationship remains unsolved. Here, using temporally controlled, PC-specific deletion of DAB1, we examined how PC migration relates to foliation. We show that postnatal DAB1 loss disrupts PC positioning and foliation in lobules VI/VII, and that even mild PC displacement from the PC layer (PCL) reduces local proliferation of granule cell precursors (GCPs), while Sonic hedgehog (SHH) supplementation rescues these foliation defects. Furthermore, we find that PC arrival at the PCL differs across lobules, accompanied by lobule-specific peaks in GCP proliferation. These findings identify PC arrival at the PCL as a developmental process that enables effective SHH signaling, thereby promoting foliation, and indicate that spatial differences in PC arrival timing orchestrate the temporal sequence of cerebellar foliation.

iScienceVol. 29(9)
University of Occupational and Environmental Health Japan (JP), Keio University Hospital (JP)
Takeda Science Foundation, Asahi Glass Foundation, Japan Agency for Medical Research and Development, Keio University, Japan Society for the Promotion of Science, Japan Science and Technology Agency
Openalex Percentile: Top 15%
Neurogenesis and neuroplasticity mechanisms
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