A single-cell transcriptional atlas reveals resident progenitor cell niche functions in TMJ disc development and injury.
Ruiye BiQing YinHaohan LiXianni YangYiru WangQianli LiHan FangPeiran LiPing LyuYi FanBinbin YingSongsong ZhuPublished in: Nature communications (2023)
The biological characteristics of the temporomandibular joint disc involve complex cellular network in cell identity and extracellular matrix composition to modulate jaw function. The lack of a detailed characterization of the network severely limits the development of targeted therapies for temporomandibular joint-related diseases. Here we profiled single-cell transcriptomes of disc cells from mice at different postnatal stages, finding that the fibroblast population could be divided into chondrogenic and non-chondrogenic clusters. We also find that the resident mural cell population is the source of disc progenitors, characterized by ubiquitously active expression of the NOTCH3 and THY1 pathways. Lineage tracing reveals that Myh11 + mural cells coordinate angiogenesis during disc injury but lost their progenitor characteristics and ultimately become Sfrp2 + non-chondrogenic fibroblasts instead of Chad + chondrogenic fibroblasts. Overall, we reveal multiple insights into the coordinated development of disc cells and are the first to describe the resident mural cell progenitor during disc injury.
Keyphrases
- single cell
- rna seq
- extracellular matrix
- mesenchymal stem cells
- high throughput
- induced apoptosis
- cell cycle arrest
- patient safety
- cell therapy
- gene expression
- poor prognosis
- type diabetes
- adipose tissue
- cell proliferation
- dna methylation
- genome wide
- signaling pathway
- preterm infants
- quality improvement
- endothelial cells
- left ventricular
- long non coding rna
- transcription factor
- metabolic syndrome
- skeletal muscle
- cell death
- hypertrophic cardiomyopathy
- pi k akt
- network analysis