Dasuri Kalavathi, Nguyen Anhthao, Zhang Le, Fernandez-Kim Ok Sun, Bruce-Keller Annadora J, Blalock Bradford A, Cabo Rafael De, Keller Jeffrey N
Pennington Biomedical Research Center/Louisiana State University System, Baton Rouge, LA 70808-4124, USA.
Free Radic Res. 2009 Jan;43(1):28-36. doi: 10.1080/10715760802534812.
The present study examined brain and liver derived proteasome complexes to elucidate if there is a differential susceptibility in proteasome complexes from these tissues to undergo inactivation following exposure to oxidative stressors. It then examined the influence of ageing and dietary restriction (DR) on the observed proteasome inactivation. Studies used a filtration based methodology that allows for enrichment of proteasome complexes with less tissue than is required for traditional chromatography procedures. The results indicate that the brain has much lower levels of overall proteasome activity and exhibits increased sensitivity to hydrogen peroxide mediated inactivation as compared to proteasome complexes derived from the liver. Interestingly, the brain proteasome complexes did not appear to have increased susceptibility to 4-hydroxynonenal (HNE)-induced inactivation. Surprisingly, ageing and DR induced minimal effects on oxidative stress mediated proteasome inhibition. These results indicate that the brain not only has lower levels of proteasome activity compared to the liver, but is also more susceptible to inactivation following exposure to some (but certainly not all) oxidative stressors. This data also suggest that ageing and DR may not significantly modulate the resistance of the proteasome to inactivation in some experimental settings.
本研究检测了脑和肝脏来源的蛋白酶体复合物,以阐明这些组织中的蛋白酶体复合物在暴露于氧化应激源后是否存在失活敏感性差异。随后,研究了衰老和饮食限制(DR)对观察到的蛋白酶体失活的影响。研究采用了基于过滤的方法,该方法能够在比传统色谱法所需组织量更少的情况下富集蛋白酶体复合物。结果表明,与肝脏来源的蛋白酶体复合物相比,脑内蛋白酶体的总体活性水平要低得多,并且对过氧化氢介导的失活表现出更高的敏感性。有趣的是,脑蛋白酶体复合物对4-羟基壬烯醛(HNE)诱导的失活似乎没有增加的敏感性。令人惊讶的是,衰老和DR对氧化应激介导的蛋白酶体抑制作用产生的影响极小。这些结果表明,与肝脏相比,脑内不仅蛋白酶体活性水平较低,而且在暴露于某些(但肯定不是所有)氧化应激源后更容易失活。该数据还表明,在某些实验条件下,衰老和DR可能不会显著调节蛋白酶体对失活的抗性。