The temporal expression of estrogen receptor alpha-36 and runx2 in human bone marrow derived mesenchymal stromal cells during osteogenesis

被引:5
作者
Francis, W. R. [1 ]
Owens, S. E. [1 ]
Wilde, C. [1 ]
Pallister, I. [1 ,2 ]
Kanamarlapudi, V. [1 ]
Zou, W. [3 ,4 ]
Xia, Z. [1 ]
机构
[1] Swansea Univ, Coll Med, Inst Life Sci, Swansea SA2 8PP, W Glam, Wales
[2] Morriston Hosp, Swansea, W Glam, Wales
[3] Liaoning Normal Univ, Coll Life Sci, Dalian 116081, Peoples R China
[4] Liaoning Key Labs Biotechnol & Mol Drug Res & Dev, Dalian 116081, Peoples R China
基金
英国生物技术与生命科学研究理事会; 中国国家自然科学基金;
关键词
Bone marrow derived stromal cells (BMSC); Estrogen receptor (ER); Runt-related transcription factor-2 (runx2); Osteogenesis; ER-ALPHA; VARIANT;
D O I
10.1016/j.bbrc.2014.09.111
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
During bone maintenance in vivo, estrogen signals through estrogen receptor (ER)-alpha. The objectives of this study were to investigate the temporal expression of ER alpha 36 and ascertain its functional relevance during osteogenesis in human bone marrow derived stromal cells (BMSC). This was assessed in relation to runt-related transcription factor-2 (runx2), a main modulatory protein involved in bone formation. ER alpha 36 and runx2 subcellular localisation was assessed using immunocytochemistry, and their mRNA expression levels by real time PCR throughout the process of osteogenesis. The osteogenically induced BMSCs demonstrated a rise in ERct36 mRNA during proliferation followed by a decline in expression at day 10, which represents a change in dynamics within the culture between the proliferative stage and the differentiative stage. The mRNA expression profile of runx2 mirrored that of ER alpha 36 and showed a degree subcellular co-localisation with ER alpha 36. This study suggests that ER alpha 36 is involved in the process of osteogenesis in BMSCs, which has implications in estrogen deficient environments. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:552 / 556
页数:5
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