Identification of parathyroid hormone-regulated proteins in mouse bone marrow cells by proteomics

被引:16
作者
Kim, SH
Jun, S
Jang, HS
Lim, SK [1 ]
机构
[1] Yonsei Univ, Coll Med, Brain Korea 21 Project Med Sci, Seoul, South Korea
[2] Korea Res Inst Chem Technol, Lab Chem Genom, Bioorgan Sci Div, Taejon 305606, South Korea
[3] Yonsei Univ, Coll Med, Dept Internal Med, Div Endocrinol, Seoul, South Korea
[4] ProteomeTech, Seoul, South Korea
关键词
parathyroid hormone; bone marrow cells; proteomics;
D O I
10.1016/j.bbrc.2005.02.173
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
The ability of parathyroid hormone (PTH) to enhance bone formation has recently been exploited in the treatment of osteoporosis. Several studies have Suggested that the activation of bone marrow stromal cells could be preceded to show the anabolic effect of PTH on bone formation, but little is known of PTH-regulated proteins in bone marrow cells. Therefore, protein profiling in the intermittent PTH-treated bone marrow cells was evaluated using proteomics. Daily treatment for 5 days consisting of subcutaneous injection of either 150 mu g/kg per day of mouse PTH (1-84) or vehicle (0.9% normal saline) was performed on the ICR Mouse. At the end of the treatment period, bone marrow cells were separated and used in proteomics. The expression levels of seven proteins including vimentin were decreased, but those of four proteins including calreticulin and thioredoxin domain containing 7 protein (Txnde7) were increased. Among these, the decrease of vimentin and the increase of both calreticulin Txnde7 in mRNA levels were confirmed by semi-quantitative RT-PCR. In PTH-treated mouse MC3T3-E1 osteoblast cells, mRNA expression levels were not totally consistent with the results observed in proteomics. In conclusion, the differentially expressed proteins in bone marrow cells depending on PTH could be highly linked to the differentiation of osteoprogenitor cells in the bone marrow into preosteoblast cells. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:423 / 429
页数:7
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