Long-term self-renewing stem cells in the adult mouse hippocampus identified by intravital imaging.
Sara BottesBaptiste N JaegerGregor-Alexander PilzDavid J JörgJohn Darby ColeMerit KruseLachlan HarrisVladislav I KorobeynykIzaskun MallonaFritjof HelmchenFrançois GuillemotBenjamin David SimonsSebastian JessbergerPublished in: Nature neuroscience (2020)
Neural stem cells (NSCs) generate neurons throughout life in the mammalian hippocampus. However, the potential for long-term self-renewal of individual NSCs within the adult brain remains unclear. We used two-photon microscopy and followed NSCs that were genetically labeled through conditional recombination driven by the regulatory elements of the stem cell-expressed genes GLI family zinc finger 1 (Gli1) or achaete-scute homolog 1 (Ascl1). Through intravital imaging of NSCs and their progeny, we identify a population of Gli1-targeted NSCs showing long-term self-renewal in the adult hippocampus. In contrast, once activated, Ascl1-targeted NSCs undergo limited proliferative activity before they become exhausted. Using single-cell RNA sequencing, we show that Gli1- and Ascl1-targeted cells have highly similar yet distinct transcriptional profiles, supporting the existence of heterogeneous NSC populations with diverse behavioral properties. Thus, we here identify long-term self-renewing NSCs that contribute to the generation of new neurons in the adult hippocampus.
Keyphrases
- stem cells
- single cell
- high resolution
- cerebral ischemia
- spinal cord
- cognitive impairment
- cancer therapy
- prefrontal cortex
- induced apoptosis
- high throughput
- magnetic resonance
- dna damage
- single molecule
- optical coherence tomography
- dna methylation
- magnetic resonance imaging
- cell therapy
- multiple sclerosis
- oxidative stress
- white matter
- high speed
- signaling pathway
- blood brain barrier
- bone marrow
- photodynamic therapy
- young adults
- mass spectrometry
- fluorescence imaging
- human health
- heat shock protein
- heat shock