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Carboxyl-terminal parathyroid hormone-related protein inhibits bone resorption by isolated chicken osteoclasts.

Abstract
Carboxyl-terminal peptides from parathyroid hormone-related protein (PTHrP) have been studied for their effect on bone resorption by osteoclasts isolated from 15 day embryonic chickens. Basal bone resorption by chicken osteoclasts was directly inhibited by chicken and human PTHrP-(107-139) and the pentapeptide PTHrP-(107-111). The chicken and human analogs were equipotent. Both the number of resorption pits and the total area resorbed per bone slice were reduced by PTHrP-(107-139), but it did not alter the size of individual resorption pits. Resorption stimulated by hPTH-(1-34) in cocultures of chicken osteoclasts with osteoblasts was also inhibited by cPTHrP-(107-139) but required a concentration three orders of magnitude greater than that required to inhibit basal resorption in cocultures or cultures of isolated osteoclasts. The finding of resorption inhibitory activity by PTHrP-(107-139) in avian as well as mammalian species strengthens the hypothesis that carboxyl-terminal PTHrP may act as a paracrine regulator of bone cell activity.
AuthorsA J Fenton, T J Martin, G C Nicholson
JournalJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research (J Bone Miner Res) Vol. 9 Issue 4 Pg. 515-9 (Apr 1994) ISSN: 0884-0431 [Print] United States
PMID8030439 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Parathyroid Hormone
  • Parathyroid Hormone-Related Protein
  • Peptide Fragments
  • Proteins
  • parathyroid hormone-related protein (107-111)
  • parathyroid hormone-related protein (107-139)
  • Calcitonin
Topics
  • Animals
  • Bone Resorption (prevention & control)
  • Calcitonin (pharmacology)
  • Chick Embryo
  • Humans
  • In Vitro Techniques
  • Osteoclasts (drug effects, physiology)
  • Parathyroid Hormone (pharmacology, physiology)
  • Parathyroid Hormone-Related Protein
  • Peptide Fragments (pharmacology, physiology)
  • Proteins (pharmacology, physiology)

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