Bioengineered perfused human brain microvascular networks enhance neural progenitor cell survival, neurogenesis, and maturation.
Max A WinkelmanGuohao DaiPublished in: Science advances (2023)
Neural progenitor cells (NPCs) have the capability to self-renew and differentiate into neurons and glial cells. In the adult brain, NPCs are found near brain microvascular networks (BMVNs) in specialized microenvironments called the neurovascular niche (NVN). Although several in vitro NVN models have been previously reported, most do not properly recapitulate the intimate cellular interactions between NPCs and perfused brain microvessels. Here, we developed perfused BMVNs composed of primary human brain endothelial cells, pericytes, and astrocytes within microfluidic devices. When induced pluripotent stem cell-derived NPCs were introduced into BMVNs, we found that NPC survival, neurogenesis, and maturation were enhanced. The application of flow during BMVN coculture was also beneficial for neuron differentiation. Collectively, our work highlighted the important role of BMVNs and flow in NPC self-renewal and neurogenesis, as well as demonstrated our model's potential to study the biological and physical interactions of human NVN in vitro.
Keyphrases
- endothelial cells
- cerebral ischemia
- resting state
- high glucose
- white matter
- functional connectivity
- neural stem cells
- subarachnoid hemorrhage
- blood brain barrier
- physical activity
- spinal cord
- spinal cord injury
- diabetic rats
- cell cycle arrest
- risk assessment
- oxidative stress
- multiple sclerosis
- mental health
- free survival
- neuropathic pain
- vascular endothelial growth factor
- climate change
- network analysis
- human health