Neurological Surgery, University of Washington, Seattle, WA, USA.
Radiology, University of Washington, Seattle, WA, USA.
J Neurointerv Surg. 2019 Oct;11(10):999-1003. doi: 10.1136/neurintsurg-2018-014669. Epub 2019 Apr 12.
To study the correlation between wall shear stress and endothelial cell expression in a patient-specific, three-dimensional (3D)-printed model of a cerebral aneurysm.
A 3D-printed model of a cerebral aneurysm was created from a patient's angiogram. After populating the model with human endothelial cells, it was exposed to media under flow for 24 hours. Endothelial cell morphology was characterized in five regions of the 3D-printed model using confocal microscopy. Endothelial cells were then harvested from distinct regions of the 3D-printed model for mRNA collection and gene analysis via quantitative polymerase chain reaction (qPCR.) Cell morphology and mRNA measurement were correlated with computational fluid dynamics simulations.
The model was successfully populated with endothelial cells, which survived under flow for 24 hours. Endothelial morphology showed alignment with flow in the proximal and distal parent vessel and aneurysm neck, but disorganization in the aneurysm dome. Genetic analysis of endothelial mRNA expression in the aneurysm dome and distal parent vessel was compared with the proximal parent vessels. ADAMTS-1 and NOS3 were downregulated in the aneurysm dome, while GJA4 was upregulated in the distal parent vessel. Disorganized morphology and decreased ADAMTS-1 and NOS3 expression correlated with areas of substantially lower wall shear stress and wall shear stress gradient in computational fluid dynamics simulations.
Creating 3D-printed models of patient-specific cerebral aneurysms populated with human endothelial cells is feasible. Analysis of these cells after exposure to flow demonstrates differences in both cell morphology and genetic expression, which correlate with areas of differential hemodynamic stress.
研究脑动脉瘤患者特定的三维(3D)打印模型中壁切应力与内皮细胞表达之间的相关性。
从患者的血管造影中创建脑动脉瘤的 3D 打印模型。在用人类内皮细胞填充模型后,将其暴露于流动介质中 24 小时。使用共聚焦显微镜对 3D 打印模型的五个区域进行内皮细胞形态学特征分析。然后从 3D 打印模型的不同区域收获内皮细胞,用于 qPCR 进行 mRNA 收集和基因分析。将细胞形态和 mRNA 测量结果与计算流体动力学模拟相关联。
模型成功地填充了内皮细胞,这些细胞在流动条件下存活了 24 小时。内皮细胞形态在近段和远段母血管以及动脉瘤颈部与流动方向一致,但在动脉瘤瘤顶处出现紊乱。比较了动脉瘤瘤顶和远段母血管内皮细胞 mRNA 表达的基因分析与近段母血管。在动脉瘤瘤顶中 ADAMTS-1 和 NOS3 下调,而在远段母血管中 GJA4 上调。计算流体动力学模拟中,紊乱的形态和 ADAMTS-1 和 NOS3 表达的减少与壁切应力和壁切应力梯度显著降低的区域相关。
创建填充有人内皮细胞的患者特定脑动脉瘤 3D 打印模型是可行的。对这些细胞在暴露于流动后的分析表明,细胞形态和基因表达都存在差异,这与不同的血流动力学应激区域相关。