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基于 RGD 的皮下海绵荧光成像的体内血管生成的无创和定量评估。

Noninvasive and quantitative assessment of in vivo angiogenesis using RGD-based fluorescence imaging of subcutaneous sponges.

机构信息

Institut National de la Santé et de la Recherche Médicale INSERM, Unité 823, Institut Albert Bonniot, Grenoble, France.

出版信息

Mol Imaging Biol. 2013 Jun;15(3):239-44. doi: 10.1007/s11307-012-0595-6.

Abstract

PURPOSE

There is a real need to adapt simple and reproducible imaging methodologies to evaluate noninvasively pro- and antiangiogenic activities of new treatments in a physiological context in mice.

PROCEDURE

The angiogenic response to fibroblast growth factor 2 (FGF-2) in a model of subcutaneously implanted cellulose sponges was measured in parallel after an intravenous injection of a fluorescent αvβ3 integrin-targeting molecule (Angiolone(TM)) and an fluorescence diffuse optical tomography optical imaging system and by measuring the hemoglobin content in the sponges.

RESULTS

Optical measurements of angiogenesis correlated perfectly with the values obtained using hemoglobin quantification. This assay can be used to follow the activity of a pro- or antiangiogenic treatment like demonstrated after FGF-2 or angiostatin, respectively.

CONCLUSION

The perfectly controlled quality of cellulose sponges combined to this noninvasive optical method allow rapid, accurate, and reproducible measurements of angiogenic activities in vivo at the preclinical level.

摘要

目的

非常有必要采用简单且可重复的成像方法,在生理条件下非侵入性地评估新疗法的促血管生成和抗血管生成活性,以便用于小鼠。

方法

在皮下植入纤维素海绵模型中,通过静脉注射荧光αvβ3 整联蛋白靶向分子(Angiolone(TM))和荧光漫射光学断层成像光学成像系统,平行测量成纤维细胞生长因子 2(FGF-2)的血管生成反应,并测量海绵中的血红蛋白含量。

结果

血管生成的光学测量与使用血红蛋白定量获得的值完全吻合。该检测方法可用于跟踪促血管生成或抗血管生成治疗的活性,如分别用 FGF-2 或血管抑素处理后所观察到的那样。

结论

纤维素海绵的质量可得到完全控制,再结合这种非侵入性的光学方法,可在临床前水平快速、准确且可重复地测量体内的血管生成活性。

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