# Cover Picture

PMC · DOI: 10.1002/ame2.12397 · Animal Models and Experimental Medicine · 2024-03-25

## TL;DR

This paper explores how neural stem cells help regulate brain cells under low oxygen conditions through specific mechanisms.

## Contribution

The study reveals a novel regulatory mechanism involving miR-9 and Hes1 in neural stem cell-derived exosomes under hypoxia.

## Key findings

- Neural stem cell-derived exosomes influence endothelial cell behavior via miR-9/Hes1.
- These exosomes regulate proliferation, migration, and cell death under hypoxia.
- The findings highlight potential therapeutic applications for brain-related diseases.

## Abstract

The cover image is based on the article ‘Neural stem cell‐derived exosomes regulate cell proliferation, migration, and cell death of brain microvascular endothelial cells via the miR‐9/Hes1 axis under hypoxia’(DOI:10.1002/ame2.12394) reported by Xiaojun Deng, Xiaoyi Hu, et al. Stem cells, characterized by their undifferentiated nature, possess the remarkable ability for self‐renewal, high proliferation, anti‐inflammation and the potential to differentiate into various cell types. Stems cells, like dragons, symbolize regeneration and hope. These cells play pivotal roles in the body’s growth, development, and the onset of disease, rendering them as highly desirable targets in cell therapy.

## Linked entities

- **Genes:** Mir9 (microRNA mir-9) [NCBI Gene 100314397], HES1 (hes family bHLH transcription factor 1) [NCBI Gene 3280]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC10961854/full.md

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Source: https://tomesphere.com/paper/PMC10961854