首页> 美国卫生研究院文献>Tissue Engineering. Part A >Brain Tissue Interaction with Three-Dimensional Honeycomb Polycaprolactone-Based Scaffolds Designed for Cranial Reconstruction Following Traumatic Brain Injury
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Brain Tissue Interaction with Three-Dimensional Honeycomb Polycaprolactone-Based Scaffolds Designed for Cranial Reconstruction Following Traumatic Brain Injury

机译:脑组织与三维蜂窝状聚己内酯基支架的相互作用用于颅脑外伤后颅骨重建。

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摘要

Following traumatic brain injury (TBI), resultant voids are unable to support injections of suspension treatments, leading to ineffective healing. Moreover, without a structure to support the large defect, the defect site suffers from mechanical instability, which may impair the healing process. Therefore, having a delivery vehicle that can temporarily fill and provide mechanical support to the defect site may alleviate the healing process. In this work, we reported for the first time, the inflammatory response of brain tissue with polycaprolactone (PCL) and PCL-tricalcium phosphate (TCP) scaffolds designed and fabricated for cranial reconstruction. After cranial defects were created in Sprague-Dawley rats, PCL and PCL-TCP scaffolds were implanted for a period of 1 week and 1 month. Following histology and immunofluorescence staining with the ionized calcium binding adaptor molecule-1 (IBA-1), glial fibrillary acidic protein (GFAP), nestin, and neuronal nuclei (NeuN), results indicated that IBA-1-positive activated microglia were observed across all groups, and declined significantly by 1 month (p<0.05). Interestingly, IBA-1-positive microglia were significantly fewer in the PCL-TCP group (p<0.05), suggesting a relatively milder inflammatory response. A decrease in the number of GFAP-positive cells among all groups over time (>29%) was also observed. Initially, astrocyte hypertrophy was observed proximal to the TBI site (55% in PCL and PCL-TCP groups, 75% in control groups), but it subsided by 1 month. Proximal to the TBI site, nestin immunoreactivity was intense during week 1, and which reduced by 1 month across all groups. NeuN-positive neurons were shrunken proximal to the TBI site (<0.9 mm), 32% smaller in the PCL-TCP group and 27% smaller in the PCL group. Based on above data indicating the comparatively milder, initial inflammatory response of brain tissue to PCL-TCP scaffolds, it is suggested that PCL-TCP scaffolds have notable clinical advantages as compared to PCL scaffolds.
机译:脑外伤(TBI)后,产生的空隙无法支持悬浮疗法的注射,从而导致无效的愈合。而且,如果没有用于支撑大缺陷的结构,则缺陷部位会遭受机械不稳定的影响,这可能会损害愈合过程。因此,具有可以临时填充缺陷部位并为其提供机械支撑的输送工具可以减轻愈合过程。在这项工作中,我们首次报道了聚己内酯(PCL)和PCL-磷酸三钙(TCP)支架设计和制造用于颅骨重建的脑组织炎症反应。在Sprague-Dawley大鼠中产生颅骨缺损后,将PCL和PCL-TCP支架植入1周零1个月。用电离的钙结合衔接子分子1(IBA-1),神经胶质原纤维酸性蛋白(GFAP),巢蛋白和神经元核(NeuN)进行组织学和免疫荧光染色后,结果表明在整个组织中观察到了IBA-1阳性活化的小胶质细胞所有组,并在1个月前显着下降(p <0.05)。有趣的是,PCL-TCP组的IBA-1阳性小胶质细胞明显较少(p <0.05),表明炎症反应相对较轻。还观察到所有组中GFAP阳性细胞的数量随时间减少(> 29%)。最初,在TBI位点附近观察到星形胶质细胞肥大(PCL和PCL-TCP组为55%,对照组为75%),但在1个月后消失。在TBI部位附近,巢蛋白的免疫反应性在第1周期间非常强烈,并且在所有组中均降低了1个月。 NeuN阳性神经元在TBI位点附近收缩(<0.9mm),在PCL-TCP组中缩小了32%,在PCL组中缩小了27%。基于上述数据表明脑组织对PCL-TCP支架的相对较轻的初始炎症反应,表明PCL-TCP支架与PCL支架相比具有显着的临床优势。

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