Therapeutic avenues in bone repair: Harnessing an anabolic osteopeptide, PEPITEM, to boost bone growth and prevent bone loss

Jonathan W. Lewis, Kathryn Frost, Georgiana Neag, Mussarat Wahid, Melissa Finlay, Ellie Northall, Oladimeji Abudu, Edward Davis, Emily Powell, Charlotte Palmer, Jinsen Lu, Ed Rainger, Asif Iqbal, Myriam Chimen, Ansar Mahmood, Simon Jones, James Edwards, Amy Naylor, Helen McGettrick*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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Abstract

The existing suite of therapies for bone diseases largely act to prevent further bone loss but fail to stimulate healthy bone formation and repair. We describe an endogenous osteopeptide (PEPITEM) with anabolic osteogenic activity, regulating bone remodeling in health and disease. PEPITEM acts directly on osteoblasts through NCAM-1 signaling to promote their maturation and formation of new bone, leading to enhanced trabecular bone growth and strength. Simultaneously, PEPITEM stimulates an inhibitory paracrine loop: promoting osteoblast release of the decoy receptor osteoprotegerin, which sequesters RANKL, thereby limiting osteoclast activity and bone resorption. In disease models, PEPITEM therapy halts osteoporosis-induced bone loss and arthritis-induced bone damage in mice and stimulates new bone formation in osteoblasts derived from patient samples. Thus, PEPITEM offers an alternative therapeutic option in the management of diseases with excessive bone loss, promoting an endogenous anabolic pathway to induce bone remodeling and redress the imbalance in bone turnover.

Original languageEnglish
Article number101574
Number of pages17
JournalCell Reports Medicine
Volume5
Issue number5
DOIs
Publication statusPublished - 21 May 2024

Bibliographical note

Copyright © 2024 The Author(s). Published by Elsevier Inc.

Keywords

  • Animals
  • Humans
  • Osteoblasts/metabolism
  • Osteogenesis/drug effects
  • Mice
  • Bone Resorption/pathology
  • Anabolic Agents/pharmacology
  • Bone Remodeling/drug effects
  • Osteoporosis/pathology
  • RANK Ligand/metabolism
  • Osteoclasts/metabolism
  • Bone Development/drug effects
  • Osteoprotegerin/metabolism
  • Female
  • Signal Transduction/drug effects
  • Peptides/pharmacology
  • Male
  • Mice, Inbred C57BL
  • Bone and Bones/drug effects

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