He Wenjie, Cronstein Bruce
Division of Clinical Pharmacology, NYU School of Medicine, NYC, NY, NY 10016, USA.
Front Biosci (Elite Ed). 2011 Jun 1;3(3):888-95. doi: 10.2741/e297.
Adenosine regulates a wide variety of physiological processes including heart rate, vasodilation and inflammation through the activation of specific cell surface adenosine receptors. In addition to these well-established roles of adenosine, recent genetic and pharmacological research has implicated adenosine as an important regulator in bone remodeling. The secretion of adenosine and the presence of its four receptors in bone cells have been well documented. More recently, we provided the first evidence that adenosine regulates osteoclast formation and function through A1 receptor (A1R), and showed that A1R-knockout mice have significantly increased bone volume as a result of impaired osteoclast-mediated bone resorption. Moreover, adenosine A1R-knockout mice are protective from boss loss following ovariectomy further supporting the involvement of adenosine in osteoclast formation and function. This short review summarizes current knowledge related to the roles of adenosine and adenosine receptors in bone formation and remodeling. A deeper insight into the regulation of bone metabolism by adenosine receptors should assist in developing new therapies for osteoporosis.
腺苷通过激活特定的细胞表面腺苷受体来调节多种生理过程,包括心率、血管舒张和炎症。除了腺苷这些已被充分证实的作用外,最近的遗传学和药理学研究表明,腺苷是骨重塑的重要调节因子。骨细胞中腺苷的分泌及其四种受体的存在已得到充分证明。最近,我们首次提供证据表明,腺苷通过A1受体(A1R)调节破骨细胞的形成和功能,并表明A1R基因敲除小鼠由于破骨细胞介导的骨吸收受损,骨体积显著增加。此外,腺苷A1R基因敲除小鼠在卵巢切除术后对骨量流失具有保护作用,进一步支持了腺苷参与破骨细胞的形成和功能。这篇简短的综述总结了目前关于腺苷和腺苷受体在骨形成和重塑中作用的知识。对腺苷受体调节骨代谢的更深入了解应该有助于开发治疗骨质疏松症的新疗法。