MMP14 is a novel target of PTH signaling in osteocytes that controls resorption by regulating soluble RANKL production

Jesus Delgado-Calle, Benjamin Hancock, Elive F. Likine, Amy Y. Sato, Kevin McAndrews, Carolina Sanudo, Angela Bruzzaniti, Jose A. Riancho, James R. Tonra, Teresita Bellido

Research output: Contribution to journalArticle

8 Scopus citations


Parathyroid hormone (PTH) affects the skeleton by acting on osteocytes (Ots) inbone through yet unclear mechanisms. We report that matrix metalloproteinase 14 (MMP14) expression/activity are increased in bones from mice with genetic constitutive activation (ca) of the PTH receptor 1 (PTH1R) in Ots (caPTH1ROt) and in bones from mice exposed to elevated PTH levels but not in mice lacking [conditional knockout (cKO)] the PTH1R in Ots (cKOPTH1ROt). Furthermore, PTH upregulates MMP14 in human bone cultures and in Ot-enriched bones from floxed controlmice but not fromcKOPTH1ROt mice.MMP14 activity increases soluble receptor activator of NF-κB ligand production, which in turn, stimulates osteoclast differentiation and resorption. Pharmacologic inhibition of MMP14 activity reduced the high bone remodeling exhibited by caPTH1ROt mice or induced by chronic PTH elevation and decreased bone resorption but allowed full stimulation of bone formation induced by PTHinjections, thereby potentiating bone gain. Thus,MMP14 is a new member of the intricate gene network activated in Ots by PTH1R signaling that can be targeted to adjust the skeletal responses to PTH in favor of bone preservation.

Original languageEnglish (US)
Pages (from-to)2878-2890
Number of pages13
JournalFASEB Journal
Issue number5
StatePublished - May 2018



  • Antiresorptive
  • Osteoblasts
  • Osteoclasts
  • Osteoporosis

ASJC Scopus subject areas

  • Biotechnology
  • Biochemistry
  • Molecular Biology
  • Genetics

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