Summary: A new mouse study reveals blood vessels play a vital role in stem cell reproduction during brain development.
Blood vessels play a vital role in stem cell reproduction, enabling the brain to grow and develop in the womb, reveals new UCL research in mice.
The study, published in the Proceedings of the National Academy of Sciences and funded by Wellcome, shows that blood vessels can increase the number of neural stem cells inside a living organism. This could be important for the design of stem cell-based therapies that aim to regenerate diseased or damaged parts of the nervous system.
In the developing brain, new neurons are produced by neural stem cells in ‘neurogenic’ areas, where they have to be instructed when and how often they should divide or what type of progeny they should produce. Until now, however, the signals responsible for these instructions have remained elusive.
“We found that blood vessels play a vital role in telling neural stem cells when and how to reproduce,” explains lead author Mathew Tata (UCL Institute of Ophthalmology). “We examined neural stem cell behaviour in the brainstem of mice lacking the blood vessel protein NRP1, because this part of the brain is particularly important to control fundamental processes such as breathing and heart rate. Preventing blood vessel growth in the neurogenic areas of the brainstem interfered with normal neuron production, causing neural stem cells to lose their ability to reproduce. As a result the stem cells disappeared from the brainstem before its growth was complete, so mice lacking NRP1 ended up with smaller brainstems.”
The research provides the first evidence that blood vessels are not only important for delivering blood to the developing brain, but also play an important role in stem cell signalling.
“Blood vessels are best known for their important function in supplying oxygen and nutrients to the brain,” says senior author Christiana Ruhrberg (UCL Institute of Ophthalmology). “However, the most intriguing finding of this study was that blood vessels did not regulate neural stem cell behaviour in the brainstem simply through their role in brain oxygenation or keeping brain tissue healthy. We found that blood vessels also provide important signals that allow stem cells to reproduce for a longer period of time, before they permanently become nerve cells that cannot multiply.”
About this neurodevelopment research article
Source: Harry Dayantis – UCL Image Source: NeuroscienceNews.com image is adapted from the UCL press release. Original Research:Abstract for “Regulation of embryonic neurogenesis by germinal zone vasculature’” by Mathew Tata, Ivan Wall, Andy Joyce, Joaquim M. Vieira, Nicoletta Kessaris, and Christiana Ruhrberg in PNAS. Published online November 7 2016 doi:10.1073/pnas.1613113113
Cite This NeuroscienceNews.com Article
[cbtabs][cbtab title=”MLA”]UCL. “Blood Vessels Control Brain Growth.” NeuroscienceNews. NeuroscienceNews, 8 November 2016. <https://neurosciencenews.com/blood-vessel-neurodevelopment-5463/>.[/cbtab][cbtab title=”APA”]UCL. (2016, November 8). Blood Vessels Control Brain Growth. NeuroscienceNews. Retrieved November 8, 2016 from https://neurosciencenews.com/blood-vessel-neurodevelopment-5463/[/cbtab][cbtab title=”Chicago”]UCL. “Blood Vessels Control Brain Growth.” https://neurosciencenews.com/blood-vessel-neurodevelopment-5463/ (accessed November 8, 2016).[/cbtab][/cbtabs]
Regulation of embryonic neurogenesis by germinal zone vasculature
In the adult rodent brain, new neurons are born in two germinal regions that are associated with blood vessels, and blood vessels and vessel-derived factors are thought to regulate the activity of adult neural stem cells. Recently, it has been proposed that a vascular niche also regulates prenatal neurogenesis. Here we identify the mouse embryo hindbrain as a powerful model to study embryonic neurogenesis and define the relationship between neural progenitor cell (NPC) behavior and vessel growth. Using this model, we show that a subventricular vascular plexus (SVP) extends through a hindbrain germinal zone populated by NPCs whose peak mitotic activity follows a surge in SVP growth. Hindbrains genetically defective in SVP formation owing to constitutive NRP1 loss showed a premature decline in both NPC activity and hindbrain growth downstream of precocious cell cycle exit, premature neuronal differentiation, and abnormal mitosis patterns. Defective regulation of NPC activity was not observed in mice lacking NRP1 expression by NPCs, but instead in mice lacking NRP1 selectively in endothelial cells, yet was independent of vascular roles in hindbrain oxygenation. Therefore, germinal zone vascularization sustains NPC proliferation in the prenatal brain.
“Regulation of embryonic neurogenesis by germinal zone vasculature’” by Mathew Tata, Ivan Wall, Andy Joyce, Joaquim M. Vieira, Nicoletta Kessaris, and Christiana Ruhrberg in PNAS. Published online November 7 2016 doi:10.1073/pnas.1613113113