Pharyngeal pouches provide a niche microenvironment for arch artery progenitor specification.
Aihua MaoMingming ZhangLinwei LiJie LiuGuozhu NingYu CaoQiang WangPublished in: Development (Cambridge, England) (2021)
The paired pharyngeal arch arteries (PAAs) are transient blood vessels connecting the heart with the dorsal aorta during embryogenesis. Although PAA malformations often occur along with pharyngeal pouch defects, the functional interaction between these adjacent tissues remains largely unclear. Here, we report that pharyngeal pouches are essential for PAA progenitor specification in zebrafish embryos. We reveal that the segmentation of pharyngeal pouches coincides spatiotemporally with the emergence of PAA progenitor clusters. These pouches physically associate with pharyngeal mesoderm in discrete regions and provide a niche microenvironment for PAA progenitor commitment by expressing BMP proteins. Specifically, pouch-derived BMP2a and BMP5 are the primary niche cues responsible for activating the BMP/Smad pathway in pharyngeal mesoderm, thereby promoting progenitor specification. In addition, BMP2a and BMP5 play an inductive function in the expression of the cloche gene npas4l in PAA progenitors. cloche mutants exhibit a striking failure to specify PAA progenitors and display ectopic expression of head muscle markers in the pharyngeal mesoderm. Therefore, our results support a crucial role for pharyngeal pouches in establishing a progenitor niche for PAA morphogenesis via BMP2a/5 expression.
Keyphrases
- cell fate
- mesenchymal stem cells
- poor prognosis
- bone regeneration
- stem cells
- spinal cord
- gene expression
- binding protein
- deep learning
- genome wide
- long non coding rna
- machine learning
- skeletal muscle
- neuropathic pain
- spinal cord injury
- aortic valve
- dna methylation
- atrial fibrillation
- single cell
- copy number
- genome wide identification
- pulmonary arterial hypertension