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BERTRAND, J. Y.

Publications and source records attributed to BERTRAND, J. Y..

2 recordsLinked to original sources

Connexin 41.8 mediates the correct temporal induction of haematopoietic stem and progenitor cells

Haematopoietic stem and progenitor cells (HSPCs) derive from a subset of endothelial cells (ECs), known as haemogenic ECs by the process of endothelial-to-haematopoietic transition (EHT). Although many factors involved in EHT have been elucidated, we still have a poor understanding of the temporal regulation of this process. Mitochondrial-derived reactive oxygen species (ROS) have been shown to stabilise hypoxia-inducible factors 1/2 (Hif1/2), allowing them to positively regulate EHT. Here, we show a developmental delay in EHT and HSPC induction in a gap junction mutant, connexin (cx)41.8 (orthologous to mammalian CX40), in zebrafish. In mammalian cells, CX40 has been shown to localise to the mitochondria. We demonstrate that Cx41.8 is important for the correct temporal generation of mitochondrial ROS, which stabilise the Hif pathway, allowing for the subsequent specification of the haemogenic endothelium. Taken together, our data indicate that Cx41.8 mediates the correct induction of HSPCs.

developmental biology↗

Dlc1 controls cardio-vascular development downstream of Vegfa/Kdrl/Nrp1 signaling in the zebrafish embryo.

The family of deleted-in-liver-cancer (dlc) genes encodes RhoGTPases and plays pivotal roles in cardiovascular development, but animal models for studying their functions are sparse due to early embryonic lethality. Gain and loss of function of dlc1 and dlc3 severely altered the growth of intersegmental vessels in the trunk of zebrafish embryos. Additionally, overexpression of dlc1 affected the growth of the common cardinal veins, but could rescue the arrest of angiogenesis induced by Vegfr2 inhibition, placing dlc1 downstream of kdrl signaling. Loss of dlc1 negatively affected the lumenization of the first aortic arch arteries and the lateral dorsal aortae. dlc1 mutants displayed a full obstruction in the early outflow tract during cardiac morphogenesis, which models to alterations in DLC1 detected in congenital heart defects in human patients. This study provides a functional in vivo characterization of dlc1 and dlc3 during vertebrate embryogenesis and places dlc1 as a key gene to control vascular development.

developmental biology↗