Sanchez-Bezanilla Sonia, Nilsson Michael, Walker Frederick R, Ong Lin Kooi
School of Biomedical Sciences and Pharmacy and Priority Research Centre for Stroke and Brain Injury, The University of Newcastle, Callaghan, NSW, Australia.
Hunter Medical Research Institute, New Lambton Heights, NSW, Australia.
Front Mol Neurosci. 2019 Jul 30;12:181. doi: 10.3389/fnmol.2019.00181. eCollection 2019.
2,3,5-Triphenyltetrazolium chloride (TTC) staining is a commonly used method to determine the volume of the cerebral infarction in experimental stroke models. The TTC staining protocol is considered to interfere with downstream analyses, and it is unclear whether TTC-stained brain samples can be used for biochemistry analyses. However, there is evidence indicating that, with proper optimization and handling, TTC-stained brains may remain viable for protein analyses. In the present study, we aimed to rigorously assess whether TTC can reliably be used for western blotting of various markers. In this study, brain samples obtained from C57BL/6 male mice were treated with TTC (TTC+) or left untreated (TTC-) at 1 week after photothrombotic occlusion or sham surgery. Brain regions were dissected into infarct, thalamus, and hippocampus, and proteins were extracted by using radioimmunoprecipitation assay buffer. Protein levels of apoptosis, autophagy, neuronal, glial, vascular, and neurodegenerative-related markers were analyzed by western blotting. Our results showed that TTC+ brains display similar relative changes in most of the markers compared with TTC- brains. In addition, we validated that these analyses can be performed in the infarct as well as other brain regions such as the thalamus and hippocampus. Our findings demonstrate that TTC+ brains are reliable for protein analyses using western blotting. Widespread adoption of this approach will be key to lowering the number of animals used while maximizing data.
2,3,5-氯化三苯基四氮唑(TTC)染色是在实验性中风模型中确定脑梗死体积的常用方法。TTC染色方案被认为会干扰下游分析,目前尚不清楚TTC染色的脑样本是否可用于生化分析。然而,有证据表明,经过适当优化和处理后,TTC染色的脑样本可能仍可用于蛋白质分析。在本研究中,我们旨在严格评估TTC是否可可靠地用于各种标志物的蛋白质印迹分析。在这项研究中,在光血栓闭塞或假手术后1周,将从C57BL/6雄性小鼠获得的脑样本用TTC处理(TTC+)或不进行处理(TTC-)。将脑区解剖为梗死灶、丘脑和海马,并使用放射免疫沉淀分析缓冲液提取蛋白质。通过蛋白质印迹分析凋亡、自噬、神经元、神经胶质、血管和神经退行性相关标志物的蛋白质水平。我们的结果表明,与TTC-脑相比,TTC+脑在大多数标志物中显示出相似的相对变化。此外,我们验证了这些分析可在梗死灶以及丘脑和海马等其他脑区进行。我们的研究结果表明,TTC+脑对于使用蛋白质印迹进行蛋白质分析是可靠的。广泛采用这种方法将是减少动物使用数量同时最大化数据的关键。