Abstract
AIMS: Neural stem cells (NSCs) generate neurons and glia in the adult vertebrate brain, crucial for tissue maintenance and plasticity. They balance neurogenesis with self-renewal, regulated through transitions between quiescence, activation, and lineage progression. The molecular and cellular mechanisms behind these processes remain incompletely understood. METHODS: Here, we describe a protocol to isolate and expand NSCs from the adult zebrafish pallium, a major NSC niche. We present the procedures to propagate primary cultures of NSCs, followed by the generation of 3D spheres and their regulation in a droplet microfluidic platform. We then detail the procedure to analyze adult NSC fate within the 3D spheroids following drug treatment. RESULTS: We show that 7 µL droplets are sufficient to allow the formation of size-controlled 3D spheroids, in which NSCs sustain self-renewal and are able to balance quiescence and activation. We outline potential applications, including investigation of factors involved in adult NSC activation and monitoring of their soluble environment, for which a confined culture system is advantageous.
| Original language | English |
|---|---|
| Article number | e70007 |
| Journal | Biology of the Cell |
| Volume | 117 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - 1 Apr 2025 |
Keywords
- 3D spheroids
- adult neural stem cells
- microfluidic chips
- quiescence
- zebrafish
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