Jiang Quan, Zhang Zheng Gang, Ding Guang Liang, Zhang Li, Ewing James R, Wang Lei, Zhang RuiLan, Li Lian, Lu Mei, Meng He, Arbab Ali S, Hu Jiani, Li Qing Jiang, Pourabdollah Nejad D Siamak, Athiraman Hemanthkumar, Chopp Michael
Department of Neurology, Henry Ford Health Sciences Center, Detroit, MI 48202, USA.
Neuroimage. 2005 Nov 15;28(3):698-707. doi: 10.1016/j.neuroimage.2005.06.063. Epub 2005 Aug 19.
Using MRI, we investigated dynamic changes of brain angiogenesis after neural progenitor cell transplantation in the living adult rat subjected to embolic stroke. Neural progenitor cells isolated from the subventricular zone (SVZ) of the adult rat were labeled by superparamagnetic particles and intracisternally transplanted into the adult rat 48 h after stroke (n = 8). Before and after the transplantation, an array of MRI parameters were measured, including high resolution 3D MRI and quantitative T1, T1sat (T1 in the presence of an off-resonance irradiation of the macromolecules of brain), T2, the inverse of the apparent forward transfer rate for magnetization transfer (kinv), cerebral blood flow (CBF), cerebral blood volume (CBV), and blood-to-brain transfer constant (Ki) of Gd-DTPA. The von Willerbrand factor (vWF) immunoreactive images of coronal sections obtained at 6 weeks after cell transplantation were used to analyze vWF immunoreactive vessels. MRI measurements revealed that grafted neural progenitor cells selectively migrated towards the ischemic boundary regions. In the ischemic boundary regions, angiogenesis confirmed by an increase in vascular density and the appearance of large thin wall mother vessels was coincident with increases of CBF and CBV (CBF, P < 0.01; CBV, P < 0.01) at 6 weeks after treatment, and coincident with transient increases of K(i) with a peak at 2 to 3 weeks after cell therapy. Relative T1, T1sat, T2, and kinv decreased in the ischemic boundary regions with angiogenesis compared to that in the non-angiogenic ischemic region (T1, P < 0.01 at 6 weeks; T1sat, P < 0.05 at 2 to 6 weeks; T2, P < 0.05 at 3 to 6 weeks; kinvP < 0.05 at 6 weeks). Of these methods, Ki appear to be the most useful MR measurements which identify and predict the location and area of angiogenesis. CBF, CBV, T1sat, T1, T2, and kinv provide complementary information to characterize ischemic tissue with and without angiogenesis. Our data suggest that select MRI parameters can identify the cerebral tissue destined to undergo angiogenesis after treatment of embolic stroke with cell therapy.
我们使用磁共振成像(MRI)技术,研究了成年大鼠栓塞性中风后神经祖细胞移植后脑血管生成的动态变化。从成年大鼠脑室下区(SVZ)分离出的神经祖细胞用超顺磁性颗粒标记,并在中风后48小时经脑池内移植到成年大鼠体内(n = 8)。在移植前后,测量了一系列MRI参数,包括高分辨率3D MRI以及定量T1、T1sat(在脑大分子的非共振照射存在下的T1)、T2、磁化传递的表观正向转移率的倒数(kinv)、脑血流量(CBF)、脑血容量(CBV)以及钆喷酸葡胺(Gd-DTPA)的血脑转移常数(Ki)。利用细胞移植后6周获得的冠状切片的血管性血友病因子(vWF)免疫反应图像来分析vWF免疫反应性血管。MRI测量结果显示,移植的神经祖细胞选择性地向缺血边界区域迁移。在缺血边界区域,血管密度增加以及出现大的薄壁母血管所证实的血管生成,与治疗后6周时CBF和CBV的增加相一致(CBF,P < 0.01;CBV,P < 0.01),并且与细胞治疗后2至3周时K(i)的短暂增加以及峰值相一致。与非血管生成性缺血区域相比,血管生成的缺血边界区域的相对T1、T1sat、T2和kinv降低(T1,6周时P < 0.01;T1sat,2至6周时P < 0.05;T2,3至6周时P < 0.05;kinv,6周时P < 0.05)。在这些方法中,Ki似乎是识别和预测血管生成位置及区域的最有用的MR测量指标。CBF、CBV、T1sat、T1、T2和kinv提供了补充信息,以表征有或无血管生成的缺血组织。我们的数据表明,选择的MRI参数可以识别栓塞性中风细胞治疗后注定会发生血管生成的脑组织。