TP508 accelerates fracture repair by promoting cell growth over cell death

被引:20
作者
Li, Xinmin
Wang, Hali
Touma, Edward
Qi, Yuchen
Rousseau, Emma
Quigg, Richard J.
Ryaby, James T.
机构
[1] Shanxi Agr Univ, Coll Anim Sci & Technol, Taigu 030801, Peoples R China
[2] Univ Chicago, Div Biol Sci, Funct Genom Facil, Chicago, IL 60637 USA
[3] Zimmer Inc, Austin, TX 78726 USA
[4] Beijing Univ, Coll Life Sci, Beijing 10091, Peoples R China
[5] Ortholog Corp, Res & Dev, Tempe, AZ 85281 USA
[6] Univ Chicago, Div Biol Sci, Dept Med, Chicago, IL 60637 USA
关键词
protein expression profile; pathway analysis; bone repair; rat; protein antibody array;
D O I
10.1016/j.bbrc.2007.07.202
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
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(TM) 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-kappa B, PDGF, PI3K/AKT, PTEN, and ERK/MAPK. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:187 / 193
页数:7
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