Zaheer A, Lenkinski R E, Mahmood A, Jones A G, Cantley L C, Frangioni J V
Department of Radiology, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.
Nat Biotechnol. 2001 Dec;19(12):1148-54. doi: 10.1038/nbt1201-1148.
In vertebrates, the development and integrity of the skeleton requires hydroxyapatite (HA) deposition by osteoblasts. HA deposition is also a marker of, or a participant in, processes as diverse as cancer and atherosclerosis. At present, sites of osteoblastic activity can only be imaged in vivo using gamma-emitting radioisotopes. The scan times required are long, and the resultant radioscintigraphic images suffer from relatively low resolution. We have synthesized a near-infrared (NIR) fluorescent bisphosphonate derivative that exhibits rapid and specific binding to HA in vitro and in vivo. We demonstrate NIR light-based detection of osteoblastic activity in the living animal, and discuss how this technology can be used to study skeletal development, osteoblastic metastasis, coronary atherosclerosis, and other human diseases.
在脊椎动物中,骨骼的发育和完整性需要成骨细胞沉积羟基磷灰石(HA)。HA沉积也是癌症和动脉粥样硬化等多种过程的标志物或参与者。目前,成骨细胞活性位点只能在体内使用发射γ射线的放射性同位素进行成像。所需的扫描时间很长,并且所得的放射性核素图像分辨率相对较低。我们合成了一种近红外(NIR)荧光双膦酸盐衍生物,它在体外和体内都能快速、特异性地与HA结合。我们展示了基于近红外光的活体动物成骨细胞活性检测,并讨论了该技术如何用于研究骨骼发育、成骨细胞转移、冠状动脉粥样硬化和其他人类疾病。