Abstract

Vegfc/Vegfr3 signaling is critical for lymphangiogenesis, the sprouting of lymphatic vessels. In zebrafish, cells sprouting from the posterior cardinal vein can either form lymphatic precursor cells or contribute to intersegmental vein formation. Both, the Vegfc-dependent differential induction of Prox1a in sprouting cells as well as a Notch-mediated pre-pattern within intersegmental vessels have been associated with the regulation of secondary sprout behavior. However, how exactly a differential lymphatic versus venous sprout cell behavior is achieved is not fully understood. Here, we characterize a zebrafish mutant in the adaptor protein Grb2b, and demonstrate through genetic interaction studies that Grb2b acts within the Vegfr3 pathway. Mutant embryos exhibit phenotypes that are consistent with reduced Vegfr3 signaling outputs prior to the sprouting of endothelial cells from the vein. During secondary sprouting stages, loss of grb2b leads to defective cell behaviors resulting in a loss of parachordal lymphangioblasts, while only partially affecting the number of intersegmental veins. A second GRB2 zebrafish ortholog, grb2a, contributes to the development of lymphatic structures in the meninges and in the head, but not in the trunk. Our results illustrate an essential role of Grb2b in vivo for cell migration to the horizontal myoseptum and for the correct formation of the lymphatic vasculature, while being less critically required in intersegmental vein formation. Thus, there appear to be higher requirements for Grb2b and therefore Vegfr3 downstream signaling levels in lymphatic versus vein precursor-generating sprouts.

Highlights

  • The lymphatic vasculature is a vital organ system that covers different functions in the vertebrate body, such as trafficking of immune cells, maintenance of fluid homeostasis and absorption of dietary fat

  • We found that providing excess grb2a mRNA ubiquitously was sufficient to restore lymphatic structures in grb2bmu404 mutant embryos at 5dpf (Supplementary Fig. S5a-d)

  • The total number of nuclei did not differ among the three genotypes, suggesting that the defect is not caused by aberrant endothelial proliferation. These results indicate an impairment in the polarization of the posterior cardinal vein (PCV) prior to sprouting, which likely contributes to the strong lymphatic defects seen in grb2b mutants at 48hpf

Read more

Summary

Introduction

The lymphatic vasculature is a vital organ system that covers different functions in the vertebrate body, such as trafficking of immune cells, maintenance of fluid homeostasis and absorption of dietary fat. The other half migrates to the horizontal myoseptum (HM) to constitute a pool of lymphatic precursor cells, so-called parachordal lymphangioblasts (PLs). GRB2 constitutes an adaptor protein that acts downstream of VEGFR3, but of different tyrosine kinase receptors [17]. It contains two Src homology 3 (SH3) and one Src homology 2 (SH2) domain [17]. We demonstrate that this adaptor protein, which has been shown to bind to VEGFR3 in vitro [20], is essential for normal endothelial cell migration in the zebrafish trunk and that it has differential effects on venous versus lymphatic endothelial cell behavior

Materials and methods
Findings
Discussion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call