Single-cell reconstruction with spatial context of migrating neural crest cells and their microenvironments during vertebrate head and neck formation.
Jason A MorrisonRebecca McLennanJessica M TeddyAllison R ScottJennifer C Kasemeier-KulesaMadelaine M GogolPaul M KulesaPublished in: Development (Cambridge, England) (2021)
The dynamics of multipotent neural crest cell differentiation and invasion as cells travel throughout the vertebrate embryo remain unclear. Here, we preserve spatial information to derive the transcriptional states of migrating neural crest cells and the cellular landscape of the first four chick cranial to cardiac branchial arches (BA1-4) using label-free, unsorted single-cell RNA sequencing. The faithful capture of branchial arch-specific genes led to identification of novel markers of migrating neural crest cells and 266 invasion genes common to all BA1-4 streams. Perturbation analysis of a small subset of invasion genes and time-lapse imaging identified their functional role to regulate neural crest cell behaviors. Comparison of the neural crest invasion signature to other cell invasion phenomena revealed a shared set of 45 genes, a subset of which showed direct relevance to human neuroblastoma cell lines analyzed after exposure to the in vivo chick embryonic neural crest microenvironment. Our data define an important spatio-temporal reference resource to address patterning of the vertebrate head and neck, and previously unidentified cell invasion genes with the potential for broad impact.
Keyphrases
- single cell
- induced apoptosis
- cell cycle arrest
- genome wide
- rna seq
- bioinformatics analysis
- stem cells
- cell migration
- endoplasmic reticulum stress
- gene expression
- genome wide identification
- cell death
- healthcare
- heart failure
- signaling pathway
- label free
- social media
- cell therapy
- pregnant women
- mass spectrometry
- atrial fibrillation
- machine learning
- climate change
- artificial intelligence