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TP508 accelerates fracture repair by promoting cell growth over cell death

  • Xinmin Li
  • , Hali Wang
  • , Edward Touma
  • , Yuchen Qi
  • , Emma Rousseau
  • , Richard J. Quigg
  • , James T. Ryaby
  • Shanxi Agricultural University
  • The University of Chicago
  • Zimmer Biomet
  • Peking University
  • OrthoLogic Corp.

Research output: Contribution to journalArticlepeer-review

22 Scopus citations

Abstract

TP508 is a synthetic 23-amino acid peptide representing a receptor-binding domain of human thrombin. We have previously shown that a single injection of TP508 accelerates fracture healing in a rat femoral fracture model. To understand how TP508 acts at the protein level during fracture healing, we compared the translational profiles between saline-control and fractured femur at six time points after TP508 treatment using the second generation of BD Clontech™ Antibody Microarray. Here, we demonstrate that TP508 accelerates fracture healing by modulating expression levels of proteins primarily involved in the functional categories of cell cycle, cellular growth and proliferation, and cell death. The majority of those proteins are physically interrelated and functionally overlapped. The action of those proteins is highlighted by a central theme of promoting cell growth via balance of cell survival over cell death signals. This appears to occur through the stimulation of several bone healing pathways including cell cycle-G1/S checkpoint regulation, apoptosis, JAK/STAT, NF-κB, PDGF, PI3K/AKT, PTEN, and ERK/MAPK.

Original languageEnglish
Pages (from-to)187-193
Number of pages7
JournalBiochemical and Biophysical Research Communications
Volume364
Issue number1
DOIs
StatePublished - Dec 7 2007

Keywords

  • Bone repair
  • Pathway analysis
  • Protein antibody array
  • Protein expression profile
  • Rat

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