Loss of Lrp2 in zebrafish disrupts pronephric tubular clearance but not forebrain development

Esther Kur(Max Delbrück Center), Anna Christa(Max Delbrück Center), Kerry N. Veth(Medical College of Wisconsin), Chandresh R. Gajera(Max Delbrück Center), Miguel A. Andrade‐Navarro(Max Delbrück Center), Jingjing Zhang(Max Delbrück Center), Jason R. Willer(Duke University), Ronald G. Gregg(University of Louisville), Salim Abdelilah‐Seyfried(Max Delbrück Center), Sebastian Bachmann(Charité - Universitätsmedizin Berlin), Brian A. Link(Medical College of Wisconsin), Annette Hammes(Max Delbrück Center), Thomas E. Willnow(Max Delbrück Center)
Developmental Dynamics
March 31, 2011
Cited by 38Open Access
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Abstract

Low-density lipoprotein receptor-related protein 2 (LRP2) is a multifunctional cell surface receptor conserved from nematodes to humans. In mammals, it acts as regulator of sonic hedgehog and bone morphogenetic protein pathways in patterning of the embryonic forebrain and as a clearance receptor in the adult kidney. Little is known about activities of this LRP in other phyla. Here, we extend the functional elucidation of LRP2 to zebrafish as a model organism of receptor (dys)function. We demonstrate that expression of Lrp2 in embryonic and larval fish recapitulates the patterns seen in mammalian brain and kidney. Furthermore, we studied the consequence of receptor deficiencies in lrp2 and in lrp2b, a homologue unique to fish, using ENU mutagenesis or morpholino knockdown. While receptor-deficient zebrafish suffer from overt renal resorption deficiency, their brain development proceeds normally, suggesting evolutionary conservation of receptor functions in pronephric duct clearance but not in patterning of the teleost forebrain.


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