hCALCRL mutation causes autosomal recessive nonimmune hydrops fetalis with lymphatic dysplasia.

Published

Journal Article

We report the first case of nonimmune hydrops fetalis (NIHF) associated with a recessive, in-frame deletion of V205 in the G protein-coupled receptor, Calcitonin Receptor-Like Receptor (hCALCRL). Homozygosity results in fetal demise from hydrops fetalis, while heterozygosity in females is associated with spontaneous miscarriage and subfertility. Using molecular dynamic modeling and in vitro biochemical assays, we show that the hCLR(V205del) mutant results in misfolding of the first extracellular loop, reducing association with its requisite receptor chaperone, receptor activity modifying protein (RAMP), translocation to the plasma membrane and signaling. Using three independent genetic mouse models we establish that the adrenomedullin-CLR-RAMP2 axis is both necessary and sufficient for driving lymphatic vascular proliferation. Genetic ablation of either lymphatic endothelial Calcrl or nonendothelial Ramp2 leads to severe NIHF with embryonic demise and placental pathologies, similar to that observed in humans. Our results highlight a novel candidate gene for human congenital NIHF and provide structure-function insights of this signaling axis for human physiology.

Full Text

Duke Authors

Cited Authors

  • Mackie, DI; Al Mutairi, F; Davis, RB; Kechele, DO; Nielsen, NR; Snyder, JC; Caron, MG; Kliman, HJ; Berg, JS; Simms, J; Poyner, DR; Caron, KM

Published Date

  • September 3, 2018

Published In

Volume / Issue

  • 215 / 9

Start / End Page

  • 2339 - 2353

PubMed ID

  • 30115739

Pubmed Central ID

  • 30115739

Electronic International Standard Serial Number (EISSN)

  • 1540-9538

Digital Object Identifier (DOI)

  • 10.1084/jem.20180528

Language

  • eng

Conference Location

  • United States