Deciphering the temporal transcriptional landscape of human fetal leptomeninges

The leptomeninges play a pivotal role in the CNS, serving both as a barrier and as a conduit for fluid and cellular transport. Despite their critical functions, our understanding of leptomeningeal development and maturation during human embryogenesis remains limited. This study seeks to bridge this gap. We conducted single-nucleus RNA sequencing on leptomeningeal tissues from eight human embryos, capturing developmental stages from early fetal to late mid-fetal phases. Our bioinformatic analyses encompassed cell type classification, identification of layer-specific markers, mapping of the arachnoid barrier maturation trajectory, and joint analyses with mouse and aged human leptomeningeal single-cell RNA sequencing (scRNA-seq) datasets datasets. Key bioinformatic findings were validated through immunostaining in selected samples. Our study revealed a complex cellular heterogeneity within the developing leptomeninges, identifying distinct subpopulations of fibroblasts, immune cells and vascular cells. We mapped the transcriptomic dynamics of fibroblast cell types throughout fetal brain development, highlighting a clear maturation process from early fetal to late mid-fetal stages. Comparative analysis with mouse data allowed us to distinguish human-specific layer markers while confirming several conserved markers shared between humans and mice. Joint analysis with aged human datasets identified two unique arachnoid clusters specific to ageing leptomeninges. Moreover, we traced the developmental trajectory of the arachnoid barrier, detailing the transcriptomic shifts associated with its gradual formation. Notably, immune cells in early fetal stages were predominantly M2-type macrophages, underscoring a distinctive immune environment. Finally, we explored the molecular interactions between fibroblasts and other cell types, highlighting their coordinated roles in orchestrating leptomeningeal development. Together, our findings provide a comprehensive overview of the cellular and molecular landscape of the developing human leptomeninges.

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Publication Details

Journal
Brain
Published
2024-12-07
DOI
https://doi.org/10.1093/brain/awae397
Citations
5
Primary Topic
MicroRNA in disease regulation
Type
article
Field-Weighted Citation Impact
1.43
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article

Deciphering the temporal transcriptional landscape of human fetal leptomeninges

Shaojie Ma, Xinyu Mei, Licheng Sun, Chuantao Fang et al.
5 citations
Brain
MicroRNA in disease regulation
1.43
article

Deciphering the temporal transcriptional landscape of human fetal leptomeninges

Shaojie Ma, Xinyu Mei, Licheng Sun, Chuantao Fang, Rui Zhao, Li Li, Wei Zhang, Ping Liu, Jingjing Guo, Dashi Qi, Yi Liu, Rui Dong, Yanfeng Tan, Jianbo Xiao, Fayong Zhang
article en
5 citations

Abstract

The leptomeninges play a pivotal role in the CNS, serving both as a barrier and as a conduit for fluid and cellular transport. Despite their critical functions, our understanding of leptomeningeal development and maturation during human embryogenesis remains limited. This study seeks to bridge this gap. We conducted single-nucleus RNA sequencing on leptomeningeal tissues from eight human embryos, capturing developmental stages from early fetal to late mid-fetal phases. Our bioinformatic analyses encompassed cell type classification, identification of layer-specific markers, mapping of the arachnoid barrier maturation trajectory, and joint analyses with mouse and aged human leptomeningeal single-cell RNA sequencing (scRNA-seq) datasets datasets. Key bioinformatic findings were validated through immunostaining in selected samples. Our study revealed a complex cellular heterogeneity within the developing leptomeninges, identifying distinct subpopulations of fibroblasts, immune cells and vascular cells. We mapped the transcriptomic dynamics of fibroblast cell types throughout fetal brain development, highlighting a clear maturation process from early fetal to late mid-fetal stages. Comparative analysis with mouse data allowed us to distinguish human-specific layer markers while confirming several conserved markers shared between humans and mice. Joint analysis with aged human datasets identified two unique arachnoid clusters specific to ageing leptomeninges. Moreover, we traced the developmental trajectory of the arachnoid barrier, detailing the transcriptomic shifts associated with its gradual formation. Notably, immune cells in early fetal stages were predominantly M2-type macrophages, underscoring a distinctive immune environment. Finally, we explored the molecular interactions between fibroblasts and other cell types, highlighting their coordinated roles in orchestrating leptomeningeal development. Together, our findings provide a comprehensive overview of the cellular and molecular landscape of the developing human leptomeninges.

BrainVol. 148(6)
Tongji University (CN), Shanghai Jiao Tong University (CN), Yale University (US), Shanghai Changning Maternity and Infant Health Hospital (CN), International Peace Maternity & Child Health Hospital (CN), Shanghai Tenth People's Hospital (CN), Children's Hospital of Fudan University (CN), Shanghai Children's Hospital (CN), Huashan Hospital (CN), Yangpu Hospital of Tongji University (CN), Universidade de Vigo (ES)
Openalex Percentile: Top 17%
MicroRNA in disease regulation
1.43
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