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Imaging cell death in vivo.

机译:体内成像细胞死亡。

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摘要

A technique to image programmed cell death would be useful both in clinical care and in drug development. The most widely studied agent for the in vivo study of apoptosis is radiolabeled annexin V, an endogenous protein labeled with technectium-99m, now undergoing clinical trials in both Europe and the United States. While annexin V has been studied extensively in humans the precise mechanism(s) of uptake this agent in vivo is unclear and needs further study. Other agents are also under development, including radiolabeled forms of Z-VAD.fmk, a potent inhibitor of the enzymatic cascade intimately associated with apoptosis. In addition other technologies, such as diffusion weighted magnetic resonance imaging and magnetic resonance imaging with contrast agents, such as small paramagnetic iron oxide particles coated with peptides have also been advocated as methods to monitor apoptotic cell death. The potential applications of imaging apoptosis as a marker of early response to therapy in cancer, acute cerebral and myocardial ischemic injury and infarction, immune mediated inflammatory disease and transplant rejection are reviewed.
机译:对程序性细胞死亡进行成像的技术在临床护理和药物开发中都将是有用的。用于体内凋亡研究的最广泛研究的试剂是放射性标记的膜联蛋白V,一种被标记为99m的内源性蛋白,目前正在欧洲和美国进行临床试验。尽管膜联蛋白V已在人体中进行了广泛研究,但在体内摄取这种药物的确切机制尚不清楚,需要进一步研究。其他药物也正在开发中,包括Z-VAD.fmk的放射性标记形式,Z-VAD.fmk是与细胞凋亡密切相关的酶联级联的有效抑制剂。此外,还提出了其他技术,例如扩散加权磁共振成像和使用造影剂的磁共振成像,例如包裹有肽的小的顺磁性氧化铁小颗粒,作为监测凋亡细胞死亡的方法。综述了成像凋亡作为癌症,急性脑和心肌缺血性损伤和梗塞,免疫介导的炎性疾病和移植排斥反应中对治疗早期反应的标志物的潜在应用。

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