Expression and significance of CX3CL1 in brain tissue in mutant P301L transgenic mice
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摘要:
目的:探讨炎症趋化因子CX3CL1(fractalkine)在含突变p301L转基因小鼠脑组织中的表达及作用。方法:分别取9月龄含突变p301L转基因小鼠和9月龄野生型小鼠各10只。使用Western blot 检测小鼠脑组织中CX3CL1蛋白的表达。取脑组织制作冰冻切片,使用抗p-tau、CX3CL1 抗体行免疫荧光检测。结果:与9月龄野生型小鼠相比,9 月龄转基因小鼠的脑内CX3CL1明显上调。免疫荧光共表达结果显示CX3CL1与p-tau共表达 。结论:CX3CL1在含突变p301L转基因小鼠脑组织中表达上调,可能与tau导致的神经损伤的炎症机制有关。
Abstract:
Objective:To investigate the expression and function of CX3CL1,an inflammatory chemokine,in the brain tissue of mutant P301L transgenic mice. Methods:A total of 10 mutant P301L transgenic mice aged 9 months and 10 wild-type mice aged 9 months were selected. Western blot was used to measure the expression of CX3CL1 in brain tissue. Brain tissue samples were collected to pre-pare frozen sections,and immunofluorescence assay was performed with anti-p-tau and anti-CX3CL1 antibodies. Results:Compared with the wild-type mice,the transgenic mice had a significant increase in the expression of CX3CL1 in brain tissue. The immunofluo-rescence assay showed the co-expression of CX3CL1 and p-tau. Conclusion:CX3CL1 is significantly up-regulated in the brain tissue of mutant P301L transgenic mice and may play a role in the inflammatory mechanism of nerve injury induced by tau.