Filling a niche: Neural stem cells help maintain their microenvironment

Researchers from Tokyo Medical and Dental University (TMDU) shed new light on the characteristics of the niche in which neural stem cells reside in the developing brain

Tokyo, Japan – When it comes to cell types, stem cells have unlimited potential – literally. These self-renewing cells, which are capable of giving rise to any cell type in the body, reside in specialized microenvironments known as niches. Now, researchers in Japan have shed new insight into the dynamics of the neural stem cell niche, the home of stem cells in the brain.

In a new study published in Inflammation and Regeneration, researchers from Tokyo Medical and Dental University (TMDU) investigated the effects of hypoxic (low oxygen) conditions on the neural stem cell niche during development.

Neural stem and progenitor cells (NPSCs) give rise to the cells of the brain and nervous system. NSPCs are known to reside in a hypoxic niche, meaning that oxygen levels in the niche are lower than those of the surrounding tissues. However, the composition of this niche, and how NSPCs maintain themselves within it, is not entirely clear. The TMDU-led research team set out to investigate the effects of low oxygen conditions within the neural stem cell niche using a cell culture model of NSPCs isolated from the forebrains of embryonic mice. They cultured these cells into neurospheres, or free-floating stem cell clusters, under low-oxygen and normal-oxygen conditions.

“The results were striking, with significantly increased neurosphere formation observed under hypoxic conditions compared with normoxic conditions,” says co-lead author of the study Taichi Kashiwagi. “This led us to explore what factors play a role in the maintenance and proliferation of NSPCs under hypoxic conditions.”

The researchers evaluated a protein called vascular endothelial growth factor-A (VEGF-A) as a potential candidate. When the research team added VEGF-A to the NSPC cultures, neurosphere formation was significantly increased. Conversely, blocking VEGF-A with a drug inhibitor diminished the increase in neurosphere formation under low oxygen conditions. Additionally, VEGF-A expression was found to be upregulated in NSPCs under low oxygen conditions.

“We found that NSPCs treated with VEGF-A showed lower rates of cell death and increased cell proliferation,” says senior author Tetsuya Taga. “VEGF-A is a factor that appears to contribute to NSPC maintenance under low oxygen conditions.”

These findings indicate that NSPCs help to maintain their own population through the release of VEGF-A under hypoxic conditions. While other factors may also contribute to NSPC maintenance, these results shed new light on the composition of the neural stem cell niche during development, and may serve as a foundation for further studies of self-organization of the hypoxic niche. 

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The article, “Organization of self-advantageous niche by neural stem/progenitor cells during development via autocrine VEGF-A under hypoxia,” was published in Inflammation and Regeneration at DOI: 10.1186/s41232-022-00254-2.