Plog Benjamin A, Moll Katherine M, Kang Hongyi, Iliff Jeffrey J, Dashnaw Matthew L, Nedergaard Maiken, Vates G Edward
University of Rochester School of Medicine and Dentistry, Rochester, NY, USA; Department of Neurosurgery, Center for Translation Neuromedicine, University of Rochester Medical Center, Rochester, NY, USA; Department of Pathology, University of Rochester Medical Center, Rochester, NY, USA.
University of Rochester School of Medicine and Dentistry, Rochester, NY, USA; Department of Neurosurgery, Center for Translation Neuromedicine, University of Rochester Medical Center, Rochester, NY, USA.
J Neurosci Methods. 2014 May 30;229:44-52. doi: 10.1016/j.jneumeth.2014.04.001. Epub 2014 Apr 13.
Subarachnoid hemorrhage (SAH) is a neurologic catastrophe and poor outcome is typically attributed to vasospasm; however, there is also evidence that SAH causes a pro-inflammatory state and these two phenomena may be interrelated. SAH causes activation of microglia, but the time course and degree of microglial activation after SAH and its link to poor patient outcome and vasospasm remains unknown.
Transgenic mice expressing eGFP under the control of the CX3CR1 locus, in which microglia are endogenously fluorescent, were randomly assigned to control or SAH groups. Immunohistochemistry for CD-68 and CD-31 was performed at different time points after SAH. Using confocal microscopy and MatLab software, we have developed a novel technique to detect and quantify the stages of microglial activation and return to quiescence using an automated computerized morphometric analysis.
We detected a statistically significant decrease in microglial process complexity 2 and 7 days following SAH. In addition, we detected a statistically significant increase in microglial domain volume 1 day following SAH; however, microglial domain volume returned to baseline by 2 days.
Most techniques for microglia assessment are qualitative, not quantitative, and are therefore inadequate to address the effects of anti-inflammatory drug treatment or other therapies after SAH.
Using novel image analysis techniques we were able to reproducibly quantify activation of microglia following SAH, which will improve our ability to study the biology of microglial activation, and may ultimately improve management of disease progression and response to therapies directed at microglial activation.
蛛网膜下腔出血(SAH)是一种神经系统急症,不良预后通常归因于血管痉挛;然而,也有证据表明SAH会引发促炎状态,且这两种现象可能相互关联。SAH会导致小胶质细胞活化,但SAH后小胶质细胞活化的时间进程和程度及其与患者不良预后和血管痉挛的关联仍不清楚。
在CX3CR1基因座控制下表达绿色荧光蛋白(eGFP)的转基因小鼠,其小胶质细胞内源性荧光,被随机分为对照组或SAH组。在SAH后的不同时间点进行CD-68和CD-31的免疫组织化学检测。利用共聚焦显微镜和MatLab软件,我们开发了一种新技术,通过自动化计算机形态计量分析来检测和量化小胶质细胞活化及恢复静止的阶段。
我们检测到SAH后2天和7天小胶质细胞突起复杂性有统计学意义的降低。此外,我们检测到SAH后1天小胶质细胞域体积有统计学意义的增加;然而,小胶质细胞域体积在2天时恢复到基线水平。
大多数评估小胶质细胞的技术是定性的,而非定量的,因此不足以解决SAH后抗炎药物治疗或其他疗法的效果问题。
使用新颖的图像分析技术,我们能够可重复地量化SAH后小胶质细胞的活化,这将提高我们研究小胶质细胞活化生物学的能力,并最终可能改善疾病进展的管理以及对针对小胶质细胞活化的疗法的反应。