Jiang Xiaoyu, Yuan Liya, Engelbach John A, Cates Jeremy, Perez-Torres Carlos J, Gao Feng, Thotala Dinesh, Drzymala Robert E, Schmidt Robert E, Rich Keith M, Hallahan Dennis E, Ackerman Joseph J H, Garbow Joel R
Department of Chemistry, Washington University, St. Louis, Missouri, United States of America.
Department of Neurosurgery, Washington University, St. Louis, Missouri, United States of America.
PLoS One. 2015 Oct 6;10(10):e0139596. doi: 10.1371/journal.pone.0139596. eCollection 2015.
To develop a Gamma Knife-based mouse model of late time-to-onset, cerebral radiation necrosis (RN) with serial evaluation by magnetic resonance imaging (MRI) and histology.
Mice were irradiated with the Leksell Gamma Knife® (GK) PerfexionTM (Elekta AB; Stockholm, Sweden) with total single-hemispheric radiation doses (TRD) of 45- to 60-Gy, delivered in one to three fractions. RN was measured using T2-weighted MR images, while confirmation of tissue damage was assessed histologically by hematoxylin & eosin, trichrome, and PTAH staining.
MRI measurements demonstrate that TRD is a more important determinant of both time-to-onset and progression of RN than fractionation. The development of RN is significantly slower in mice irradiated with 45-Gy than 50- or 60-Gy, where RN development is similar. Irradiated mouse brains demonstrate all of the pathologic features observed clinically in patients with confirmed RN. A semi-quantitative (0 to 3) histologic grading system, capturing both the extent and severity of injury, is described and illustrated. Tissue damage, as assessed by a histologic score, correlates well with total necrotic volume measured by MRI (correlation coefficient = 0.948, with p<0.0001), and with post-irradiation time (correlation coefficient = 0.508, with p<0.0001).
Following GK irradiation, mice develop late time-to-onset cerebral RN histology mirroring clinical observations. MR imaging provides reliable quantification of the necrotic volume that correlates well with histologic score. This mouse model of RN will provide a platform for mechanism of action studies, the identification of imaging biomarkers of RN, and the development of clinical studies for improved mitigation and neuroprotection.
建立一种基于伽玛刀的迟发性脑放射性坏死(RN)小鼠模型,并通过磁共振成像(MRI)和组织学进行系列评估。
使用Leksell伽玛刀®PerfexionTM(医科达公司;瑞典斯德哥尔摩)对小鼠进行照射,单半球总辐射剂量(TRD)为45至60 Gy,分1至3次给予。使用T2加权MR图像测量RN,同时通过苏木精和伊红、三色染色和磷钨酸苏木精染色进行组织学评估以确认组织损伤。
MRI测量表明,TRD比分割次数更能决定RN的发病时间和进展。接受45 Gy照射的小鼠中RN的发展明显慢于接受50或60 Gy照射的小鼠,后两者的RN发展相似。照射后的小鼠大脑表现出在确诊RN患者临床中观察到的所有病理特征。描述并展示了一种半定量(0至3)组织学分级系统,该系统可反映损伤的程度和严重程度。通过组织学评分评估的组织损伤与MRI测量的总坏死体积密切相关(相关系数 = 0.948,p<0.0001),且与照射后时间相关(相关系数 = 0.508,p<0.0001)。
伽玛刀照射后,小鼠会出现迟发性脑RN组织学变化,与临床观察结果相符。MR成像可对坏死体积进行可靠定量,且与组织学评分密切相关。这种RN小鼠模型将为作用机制研究、RN成像生物标志物的鉴定以及改善缓解和神经保护临床研究的开展提供一个平台。