globalchange  > 气候变化事实与影响
DOI: 10.1289/ehp.1307832
论文题名:
Effects of Arsenic on Osteoblast Differentiation in Vitro and on Bone Mineral Density and Microstructure in Rats
作者: Cheng-Tien Wu; 1 Tung-Ying Lu; 1 Ding-Cheng Chan; 2 Keh-Sung Tsai; 3; * Rong-Sen Yang; 4; *; Shing-Hwa Liu1; 5; *
刊名: Environmental Health Perspectives
ISSN: 0091-7446
出版年: 2014
卷: Volume 122, 期:Issue 6
起始页码: 559
语种: 英语
英文摘要: Background: Arsenic is a ubiquitous toxic element and is known to contaminate drinking water in many countries. Several epidemiological studies have shown that arsenic exposure augments the risk of bone disorders. However, the detailed effect and mechanism of inorganic arsenic on osteoblast differentiation of bone marrow stromal cells and bone loss still remain unclear.

Objectives: We investigated the effects and mechanism of arsenic on osteoblast differentiation in vitro and evaluated bone mineral density (BMD) and bone microstructure in rats at doses relevant to human exposure from drinking water.

Methods: We used a cell model of rat primary bone marrow stromal cells (BMSCs) and a rat model of long-term exposure with arsenic-contaminated drinking water, and determined bone microstructure and BMD in rats by microcomputed tomography (μCT).

Results: We observed significant attenuation of osteoblast differentiation after exposure of BMSCs to arsenic trioxide (0.5 or 1 μM). After arsenic treatment during differentiation, expression of runt-related transcription factor-2 (Runx2), bone morphogenetic protein-2 (BMP-2), and osteocalcin in BMSCs was inhibited and phosphorylation of enhanced extracellular signal-regulated kinase (ERK) was increased. These altered differentiation-related molecules could be reversed by the ERK inhibitor PD98059. Exposure of rats to arsenic trioxide (0.05 or 0.5 ppm) in drinking water for 12 weeks altered BMD and microstructure, decreased Runx2 expression, and increased ERK phosphorylation in bones. In BMSCs isolated from arsenic-treated rats, osteoblast differentiation was inhibited.

Conclusions: Our results suggest that arsenic is capable of inhibiting osteoblast differentiation of BMSCs via an ERK-dependent signaling pathway and thus increasing bone loss.
URL: https://ehp.niehs.nih.gov/1307832
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资源类型: 期刊论文
标识符: http://119.78.100.158/handle/2HF3EXSE/12775
Appears in Collections:气候变化事实与影响
气候变化与战略

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作者单位: 1Institute of Toxicology, 2Department of Geriatrics and Gerontology, 3Department of Laboratory Medicine, and 4Department of Orthopaedics, College of Medicine, National Taiwan University, Taipei, Taiwan; 5Department of Medical Research, China Medical University Hospital, China Medical University, Taichung, Taiwan

*These authors contributed equally to this study.


Recommended Citation:
Cheng-Tien Wu,1 Tung-Ying Lu,1 Ding-Cheng Chan,et al. Effects of Arsenic on Osteoblast Differentiation in Vitro and on Bone Mineral Density and Microstructure in Rats[J]. Environmental Health Perspectives,2014-01-01,Volume 122(Issue 6):559
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