# Human endothelial cells promote a human neural stem cell type B phenotype via Notch signaling

**Authors:** Brenda Gutierrez, Tzu Chia Liu, Carly Rodriguez, Oier Pastor-Alonso, Hannah Lambing, Mercedes F. Paredes, Lisa A. Flanagan

PMC · DOI: 10.1038/s41467-025-60194-6 · Nature Communications · 2025-05-30

## TL;DR

Human endothelial cells help create a specific type of brain stem cell through a signaling pathway called Notch.

## Contribution

The study reveals that human endothelial cells promote type B neural stem cells via Notch signaling and identifies specific markers for these cells.

## Key findings

- Human endothelial cells increase type B neural stem cells by activating Notch signaling.
- Markers like S100A6 and LeX are identified for human type B cells.
- Type B cells and endothelial cells are found to interact in the human brain's stem cell niches.

## Abstract

Neural stem and progenitor cell (NSPC) and vessel-forming endothelial cell (EC) communication throughout development and adulthood is vital for normal brain function. However, much remains unclear regarding coordinated regulation of these cells, particularly in humans. We find that contact with hECs increases hNSPC type B cells, which are GFAP-expressing adult NSPCs in the subventricular zone (SVZ), leading to generation of a human type B single-cell RNA sequencing (scRNAseq) dataset. Differential gene expression demonstrates an increase in Notch downstream mediators in type B hNSPCs after hEC contact. Blocking hNSPC Notch signaling, and reducing hEC expression of the Notch ligand DLL4, abrogates the effect of hECs on type B hNSPCs. We identify S100A6 and LeX as human type B cell markers, and analysis of the postnatal human SVZ confirms co-expression of GFAP, SOX2, S100A6, LeX and PROM1 in type B cells. Sites of contact are identified between type B hNSPCs and vasculature in the SVZ, providing evidence of human type B cell contact with hECs in the postnatal human brain. Thus, hEC contact promotes human type B cells via Notch signaling and these cells are in contact in stem cell niches in the human brain.

Brain neural stem cell (NSC) and vessel-forming endothelial cell (EC) communication is vital. Here, the authors find that human ECs boost human adult NSCs (type B cells) via Notch, show EC-type B interaction in human brain, and identify human type B markers.

## Linked entities

- **Genes:** GFAP (glial fibrillary acidic protein) [NCBI Gene 2670], SOX2 (SRY-box transcription factor 2) [NCBI Gene 6657], S100A6 (S100 calcium binding protein A6) [NCBI Gene 6277], PROM1 (prominin 1) [NCBI Gene 8842]
- **Proteins:** Notch (neurogenic locus notch homolog), DLL4 (delta like canonical Notch ligand 4), FUT4 (fucosyltransferase 4)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** S100A6 (S100 calcium binding protein A6) [NCBI Gene 6277] {aka 2A9, 5B10, CABP, CACY, PRA, S10A6}, GFAP (glial fibrillary acidic protein) [NCBI Gene 2670] {aka ALXDRD}, DLL4 (delta like canonical Notch ligand 4) [NCBI Gene 54567] {aka AOS6, delta4, hdelta2}, PROM1 (prominin 1) [NCBI Gene 8842] {aka AC133, CD133, CORD12, MCDR2, MSTP061, PROML1}, FUT4 (fucosyltransferase 4) [NCBI Gene 2526] {aka CD15, ELFT, FCT3A, FUC-TIV, FUTIV, LeX}, SOX2 (SRY-box transcription factor 2) [NCBI Gene 6657] {aka ANOP3, MCOPS3}
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12125299/full.md

## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12125299/full.md

## References

3 references — full list in the complete paper: https://tomesphere.com/paper/PMC12125299/full.md

---
Source: https://tomesphere.com/paper/PMC12125299