Heterogeneity of the adult mammalian forebrain neurogenic ependyma: A comprehensive cellular map

JOURNAL/nrgr/04.03/01300535-202606000-00059/figure1/v/2026-02-11T151048Z/r/image-tiff The presence or absence of adult neural stem cells in the mammalian forebrain ependyma has been debated for two decades. In this study, we performed single-cell RNA sequencing to investigate the cellular composition of the ependymal surface of the adult mouse forebrain using whole mounts of lateral walls of lateral ventricles. We identified 12 different cell subtypes in the ependymal surface. Immunocytochemical analyses revealed that CD133 + multi-ciliated cells comprised 67.6% of ependymal cells, while the remaining 32.4% were CD133 - . CD133 + ependymal cells can be further classified into FOXJ1 + /SOX2 + /ACTA2 + cells, FLT1 + /CD31 + /CLDN5 + endothelial-like cells, and PDGFRB + /VTN + /NG2 + pericyte-like cells, as well as endothelial-pericyte-like cells and Foxj1+ endothelial-like cells. CD133 - ependymal cells can be further divided into endothelial-like cells, Foxj1+ ependymal cells, Foxj1+ endothelial-like cells, pericyte-like cells, endothelial-pericyte-like cells, VIM + cells, and cells negative for all of these markers. This comprehensive profiling confirms the heterogeneity of the ependymal surface in the adult mouse forebrain. Debate regarding whether adult ependymal cells contain neural stem cells has arisen because different researchers have examined different populations of ependymal cells. Our study provides a new perspective for investigation of clinical endogenous neural stem cells, ultimately paving the way for stem cell therapies in neurological diseases.

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Publication Details

Journal
Neural Regeneration Research
Published
2025-04-29
DOI
https://doi.org/10.4103/nrr.nrr-d-24-00789
Primary Topic
Glioma Diagnosis and Treatment
Type
article
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article

Heterogeneity of the adult mammalian forebrain neurogenic ependyma: A comprehensive cellular map

Liqiang Zhou, Yi Eve Sun, Qifei Wu, Yuchen Mu et al.
Neural Regeneration Research
Glioma Diagnosis and Treatment
article

Heterogeneity of the adult mammalian forebrain neurogenic ependyma: A comprehensive cellular map

Liqiang Zhou, Yi Eve Sun, Qifei Wu, Yuchen Mu, Orion Fan, Quan Lin, Wenmin Zhu, Xuejiao Yang
article en

Abstract

JOURNAL/nrgr/04.03/01300535-202606000-00059/figure1/v/2026-02-11T151048Z/r/image-tiff The presence or absence of adult neural stem cells in the mammalian forebrain ependyma has been debated for two decades. In this study, we performed single-cell RNA sequencing to investigate the cellular composition of the ependymal surface of the adult mouse forebrain using whole mounts of lateral walls of lateral ventricles. We identified 12 different cell subtypes in the ependymal surface. Immunocytochemical analyses revealed that CD133 + multi-ciliated cells comprised 67.6% of ependymal cells, while the remaining 32.4% were CD133 - . CD133 + ependymal cells can be further classified into FOXJ1 + /SOX2 + /ACTA2 + cells, FLT1 + /CD31 + /CLDN5 + endothelial-like cells, and PDGFRB + /VTN + /NG2 + pericyte-like cells, as well as endothelial-pericyte-like cells and Foxj1+ endothelial-like cells. CD133 - ependymal cells can be further divided into endothelial-like cells, Foxj1+ ependymal cells, Foxj1+ endothelial-like cells, pericyte-like cells, endothelial-pericyte-like cells, VIM + cells, and cells negative for all of these markers. This comprehensive profiling confirms the heterogeneity of the ependymal surface in the adult mouse forebrain. Debate regarding whether adult ependymal cells contain neural stem cells has arisen because different researchers have examined different populations of ependymal cells. Our study provides a new perspective for investigation of clinical endogenous neural stem cells, ultimately paving the way for stem cell therapies in neurological diseases.

Neural Regeneration ResearchVol. 21(6)
Tongji University (CN), University of California, Los Angeles (US), Shanghai East Hospital (CN), Tongji Hospital (CN)
Openalex Percentile: Top 72%
Glioma Diagnosis and Treatment
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