Macrophage-stimulating protein and calcium homeostasis in zebrafish

L.F. Huitema, J. Renn, I. Logister, J.K. Gray, S.E. Waltz, G. Flik, S. Schulte-Merker

Research output: Contribution to journal/periodicalArticleScientificpeer-review

Abstract

To systematically identify novel gene functions essential for osteogenesis and skeletal mineralization, we performed a forward genetic mutagenesis screen in zebrafish and isolated a mutant that showed delayed skeletal mineralization. Analysis of the mutant phenotype in an osterix:nuclear-GFP transgenic background demonstrated that mutants contain osterix-expressing osteoblasts comparable to wild-type embryos. Positional cloning revealed a premature stop mutation in the macrophage-stimulating protein (msp) gene, predicted to result in a biologically inactive protein. Analysis of the embryonic expression pattern for the receptor for Msp, Ron, shows specific expression in the corpuscles of Stannius, a teleost-specific organ that produces stanniocalcin, a pivotal hormone in fish calcium homeostasis. Knockdown of Ron resulted in identical phenotypes as observed in msp mutants. Msp mutant embryos could be rescued by excess calcium. Consistent with a role for Msp/Ron in calcium homeostasis, calcium-regulating factors, such as pth1, pth2, stc1l, and trpv5/6 were significantly affected in msp mutant larvae. While Msp and Ron have previously been shown to play a critical role in a wide variety of biological processes, we introduce here the Msp/Ron signaling axis as a previously unappreciated player in calcium homeostasis and embryonic skeletal mineralization.
Original languageEnglish
Pages (from-to)4092-4101
JournalFASEB Journal
Volume26
Issue number10
DOIs
Publication statusPublished - 2012

Fingerprint

Dive into the research topics of 'Macrophage-stimulating protein and calcium homeostasis in zebrafish'. Together they form a unique fingerprint.

Cite this