Abstract

Humans lacking sclerostin display progressive bone overgrowth due to increased bone formation. Although it is well established that sclerostin is an osteocyte-secreted bone formation inhibitor, the underlying molecular mechanisms are not fully elucidated. We identified in tandem affinity purification proteomics screens LRP4 (low density lipoprotein-related protein 4) as a sclerostin interaction partner. Biochemical assays with recombinant proteins confirmed that sclerostin LRP4 interaction is direct. Interestingly, in vitro overexpression and RNAi-mediated knockdown experiments revealed that LRP4 specifically facilitates the previously described inhibitory action of sclerostin on Wnt1/β-catenin signaling. We found the extracellular β-propeller structured domain of LRP4 to be required for this sclerostin facilitator activity. Immunohistochemistry demonstrated that LRP4 protein is present in human and rodent osteoblasts and osteocytes, both presumed target cells of sclerostin action. Silencing of LRP4 by lentivirus-mediated shRNA delivery blocked sclerostin inhibitory action on in vitro bone mineralization. Notably, we identified two mutations in LRP4 (R1170W and W1186S) in patients suffering from bone overgrowth. We found that these mutations impair LRP4 interaction with sclerostin and its concomitant sclerostin facilitator effect. Together these data indicate that the interaction of sclerostin with LRP4 is required to mediate the inhibitory function of sclerostin on bone formation, thus identifying a novel role for LRP4 in bone.

Highlights

  • Humans lacking sclerostin display progressive bone overgrowth due to increased bone formation

  • We identified in tandem affinity purification proteomics screens LRP4 as a sclerostin interaction partner

  • The following information is provided for the known interaction partner LRP5 and LRP6 as well as for the newly identified LRP4: representative International Protein Index (IPI) accession number, Entrez gene name, number of total spectral matches to the protein, and distinct identified peptide sequences

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Summary

Introduction

Humans lacking sclerostin display progressive bone overgrowth due to increased bone formation. We identified two mutations in LRP4 (R1170W and W1186S) in patients suffering from bone overgrowth We found that these mutations impair LRP4 interaction with sclerostin and its concomitant sclerostin facilitator effect. In vitro studies demonstrated that LRP5 high bone mass mutations have an impaired interaction with the Wnt/␤-catenin signaling inhibitors DKK1 and SOST (sclerostin) (4, 9 –12). Patients afflicted by sclerosteosis (OMIM269500) or Van Buchem disease (OMIM239100) display lifelong massive bone overgrowth with increased BMD and bone strength due to lack of sclerostin protein. It is thought that sclerostin passes through the osteocytic canalicular network to inhibit osteoblastic canonical Wnt/␤-catenin signaling by binding to the Wnt co-receptors LRP5 and LRP6. We report that the interaction between sclerostin and LRP4 (low density lipoprotein-related protein 4) is crucial to mediate the inhibitory function of sclerostin on Wnt1/␤-catenin signaling and on bone formation. We describe the identification of LRP4 mutations, which are associated with bone overgrowth and impaired sclerostin facilitator function

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