Hanak Brian W, Ross Emily F, Harris Carolyn A, Browd Samuel R, Shain William
Center for Integrative Brain Research, Seattle Children's Research Institute;
Department of Neurological Surgery, University of Washington, Seattle, Washington; and.
J Neurosurg Pediatr. 2016 Aug;18(2):213-23. doi: 10.3171/2016.2.PEDS15531. Epub 2016 Apr 1.
OBJECTIVE Shunt obstruction by cells and/or tissue is the most common cause of shunt failure. Ventricular catheter obstruction alone accounts for more than 50% of shunt failures in pediatric patients. The authors sought to systematically collect explanted ventricular catheters from the Seattle Children's Hospital with a focus on elucidating the cellular mechanisms underlying obstruction. METHODS In the operating room, explanted hardware was placed in 4% paraformaldehyde. Weekly, samples were transferred to buffer solution and stored at 4°C. After consent was obtained for their use, catheters were labeled using cell-specific markers for astrocytes (glial fibrillary acidic protein), microglia (ionized calcium-binding adapter molecule 1), and choroid plexus (transthyretin) in conjunction with a nuclear stain (Hoechst). Catheters were mounted in custom polycarbonate imaging chambers. Three-dimensional, multispectral, spinning-disk confocal microscopy was used to image catheter cerebrospinal fluid-intake holes (10× objective, 499.2-μm-thick z-stack, 2.4-μm step size, Olympus IX81 inverted microscope with motorized stage and charge-coupled device camera). Values are reported as the mean ± standard error of the mean and were compared using a 2-tailed Mann-Whitney U-test. Significance was defined at p < 0.05. RESULTS Thirty-six ventricular catheters have been imaged to date, resulting in the following observations: 1) Astrocytes and microglia are the dominant cell types bound directly to catheter surfaces; 2) cellular binding to catheters is ubiquitous even if no grossly visible tissue is apparent; and 3) immunohistochemical techniques are of limited utility when a catheter has been exposed to Bugbee wire electrocautery. Statistical analysis of 24 catheters was performed, after excluding 7 catheters exposed to Bugbee wire cautery, 3 that were poorly fixed, and 2 that demonstrated pronounced autofluorescence. This analysis revealed that catheters with a microglia-dominant cellular response tended to be implanted for shorter durations (24.7 ± 6.7 days) than those with an astrocyte-dominant response (1183 ± 642 days; p = 0.027). CONCLUSIONS Ventricular catheter occlusion remains a significant source of shunt morbidity in the pediatric population, and given their ability to intimately associate with catheter surfaces, astrocytes and microglia appear to be critical to this pathophysiology. Microglia tend to be the dominant cell type on catheters implanted for less than 2 months, while astrocytes tend to be the most prevalent cell type on catheters implanted for longer time courses and are noted to serve as an interface for the secondary attachment of ependymal cells and choroid plexus.
目的 细胞和/或组织导致的分流梗阻是分流失败最常见的原因。仅脑室导管梗阻就占小儿患者分流失败的50%以上。作者试图系统地收集西雅图儿童医院取出的脑室导管,重点是阐明梗阻背后的细胞机制。方法 在手术室中,将取出的硬件置于4%多聚甲醛中。每周将样本转移至缓冲溶液中,并于4℃保存。在获得使用许可后,使用针对星形胶质细胞(胶质纤维酸性蛋白)、小胶质细胞(离子钙结合衔接分子1)和脉络丛(转甲状腺素蛋白)的细胞特异性标志物并结合核染色(Hoechst)对导管进行标记。将导管安装在定制的聚碳酸酯成像室中。使用三维、多光谱、旋转盘共聚焦显微镜对导管脑脊液入口孔进行成像(10倍物镜,499.2μm厚的z轴堆叠,2.4μm步长,配备电动载物台和电荷耦合器件相机的奥林巴斯IX81倒置显微镜)。数值以平均值±平均标准误表示,并使用双尾曼-惠特尼U检验进行比较。显著性定义为p<0.05。结果 迄今为止,已对36根脑室导管进行成像,得出以下观察结果:1)星形胶质细胞和小胶质细胞是直接与导管表面结合的主要细胞类型;2)即使没有明显可见的组织,细胞与导管的结合也普遍存在;3)当导管暴露于Bugbee线电灼时,免疫组织化学技术的效用有限。在排除7根暴露于Bugbee线烧灼的导管、3根固定不佳的导管和2根显示明显自发荧光的导管后,对24根导管进行了统计分析。该分析显示,以小胶质细胞为主的细胞反应的导管植入时间(24.7±6.7天)往往比以星形胶质细胞为主的反应的导管(1183±642天;p=0.027)短。结论 脑室导管阻塞仍然是小儿人群分流发病的重要原因,鉴于星形胶质细胞和小胶质细胞能够与导管表面紧密结合,它们似乎对这种病理生理学至关重要。小胶质细胞往往是植入时间少于2个月的导管上的主要细胞类型,而星形胶质细胞往往是植入时间较长的导管上最普遍的细胞类型,并且被认为是室管膜细胞和脉络丛二次附着的界面。