Department of Orthopaedics, Institute of Orthopaedics, The First Affiliated Hospital of Chinese People's Liberation Army General Hospital, Beijing, China.
Biochem Biophys Res Commun. 2012 Mar 23;419(4):774-8. doi: 10.1016/j.bbrc.2012.02.100. Epub 2012 Feb 27.
The aim of current study was to elucidate whether aquaporin-9 (AQP9) expression was involved in the progression of bone loss induced by microgravity. We used the hind-limb suspension (HLS) mice model to simulate microgravity and induce bone loss. It was found that HLS exposure decreased femur bone mineral density (BMD), and enhanced femur AQP9 mRNA and protein levels. Then, the relationship between AQP9 mRNA expression and BMD was studied and it was showed that femur AQP9 mRNA level was negatively related to femur BMD in mice exposed to HLS. We sought to exam the function of AQP9 in the femur using the AQP9-null mice. It was found that AQP9 knockout attenuated bone loss and inhibited osteoclastogenesis under the condition of HLS exposure, but had no similar effect on bone under normal physiological conditions. In addition, it was found that exposure to simulated hypergravity or exercise training, main countermeasures against microgravity, reduced AQP9 mRNA and protein levels in femur of mice. Moreover, it was found that both aging and estrogen deprivation, another two risk factors of bone loss, had no significant effect on femur AQP9 expression. In conclusion, AQP9 plays an important role in the development of microgravity-induced bone loss, and may be a potential target for the prevention or management of microgravity-induced bone loss.
本研究旨在阐明水通道蛋白 9(AQP9)的表达是否参与了微重力诱导的骨丢失的进展。我们使用后肢悬吊(HLS)小鼠模型来模拟微重力并诱导骨丢失。结果发现,HLS 暴露降低了股骨骨密度(BMD),并增强了股骨 AQP9 mRNA 和蛋白水平。然后,研究了 AQP9 mRNA 表达与 BMD 之间的关系,结果表明,在暴露于 HLS 的小鼠中,股骨 AQP9 mRNA 水平与股骨 BMD 呈负相关。我们试图使用 AQP9 缺失小鼠来研究 AQP9 在股骨中的功能。结果发现,AQP9 敲除在 HLS 暴露下减轻了骨丢失并抑制了破骨细胞生成,但对正常生理条件下的骨没有类似作用。此外,发现模拟的高重力或运动训练(对抗微重力的主要对策)降低了小鼠股骨中的 AQP9 mRNA 和蛋白水平。此外,发现衰老和雌激素剥夺(骨丢失的另外两个危险因素)对股骨 AQP9 表达没有显著影响。总之,AQP9 在微重力诱导的骨丢失的发展中起重要作用,可能是预防或治疗微重力诱导的骨丢失的潜在靶点。