Axon guidance genes control hepatic artery development.
Lila GannounCatalina De SchrevelMorgane BelleNicolas DauguetYounes AchouriAxelle LoriotChristophe VanderaaSabine CordiAlexandra DiliYves HeremansIlse RoomanIsabelle A LeclercqPatrick JacqueminLaurent GattoFrédéric P LemaigrePublished in: Development (Cambridge, England) (2023)
Earlier data on liver development demonstrated that morphogenesis of the bile duct, portal mesenchyme and hepatic artery is interdependent, yet how this interdependency is orchestrated remains unknown. Here, using 2D and 3D imaging, we first describe how portal mesenchymal cells organize to form hepatic arteries. Next, we searched for intercellular signalling active during portal area development and found that axon guidance genes are dynamically expressed in developing bile ducts and portal mesenchyme. Using tissue-specific gene inactivation in mice, we show that the Repulsive guidance molecule BMP co-receptor A (Rgma)/Neogenin 1 (Neo1) receptor/ligand pair is dispensable for portal area development, but that deficient Roundabout 2 (Robo2)/Slit2 signalling in the portal mesenchyme causes reduced maturation of the vascular smooth muscle cells that form the tunica media of the hepatic artery. This arterial anomaly does not impact liver function in homeostatic condition but is associated with significant tissular damage following partial hepatectomy. In conclusion, our work identifies new players in development of the liver vasculature in health and liver regeneration.
Keyphrases
- genome wide
- vascular smooth muscle cells
- stem cells
- healthcare
- high resolution
- angiotensin ii
- metabolic syndrome
- type diabetes
- bone marrow
- adipose tissue
- skeletal muscle
- cell proliferation
- social media
- deep learning
- cell death
- photodynamic therapy
- binding protein
- insulin resistance
- cell adhesion
- fluorescence imaging
- genome wide analysis
- liver metastases