Ieraci Alessandro, Mallei Alessandra, Musazzi Laura, Popoli Maurizio
Laboratory of Neuropsychopharmacology and Functional Neurogenomics, Dipartimento di Scienze Farmacologiche e Biomolecolari and CEND, Università degli Studi di Milano, Milano, Italy.
Hippocampus. 2015 Nov;25(11):1380-92. doi: 10.1002/hipo.22458. Epub 2015 Apr 15.
Physical exercise and stressful experiences have been shown to exert opposite effects on behavioral functions and brain plasticity, partly by involving the action of brain-derived neurotrophic factor (BDNF). Although epigenetic modifications are known to play a pivotal role in the regulation of the different BDNF transcripts, it is poorly understood whether epigenetic mechanisms are also implied in the BDNF modulation induced by physical exercise and stress. Here, we show that total BDNF mRNA levels and BDNF transcripts 1, 2, 3, 4, 6, and 7 were reduced immediately after acute restraint stress (RS) in the hippocampus of mice, and returned to control levels 24 h after the stress session. On the contrary, exercise increased BDNF mRNA expression and counteracted the stress-induced decrease of BDNF transcripts. Physical exercise-induced up-regulation of BDNF transcripts was accounted for by increase in histone H3 acetylated levels at specific BDNF promoters, whereas the histone H3 trimethylated lysine 27 and dimethylated lysine 9 levels were unaffected. Acute RS did not change the levels of acetylated and methylated histone H3 at the BDNF promoters. Furthermore, we found that physical exercise and RS were able to differentially modulate the histone deacetylases mRNA levels. Finally, we report that a single treatment with histone deacetylase inhibitors, prior to acute stress exposure, prevented the down-regulation of total BDNF and BDNF transcripts 1, 2, 3, and 6, partially reproducing the effect of physical exercise. Overall, these results suggest that physical exercise and stress are able to differentially modulate the expression of BDNF transcripts by possible different epigenetic mechanisms.
体育锻炼和应激经历已被证明对行为功能和大脑可塑性具有相反的影响,部分原因是涉及脑源性神经营养因子(BDNF)的作用。虽然已知表观遗传修饰在不同BDNF转录本的调控中起关键作用,但对于体育锻炼和应激诱导的BDNF调节中是否也涉及表观遗传机制,人们了解甚少。在此,我们表明,在小鼠海马体中,急性束缚应激(RS)后,BDNF总mRNA水平以及BDNF转录本1、2、3、4、6和7立即降低,并在应激结束后24小时恢复到对照水平。相反,运动增加了BDNF mRNA表达,并抵消了应激诱导的BDNF转录本减少。体育锻炼诱导的BDNF转录本上调是由特定BDNF启动子处组蛋白H3乙酰化水平增加所致,而组蛋白H3三甲基化赖氨酸27和二甲基化赖氨酸9水平未受影响。急性RS并未改变BDNF启动子处乙酰化和甲基化组蛋白H3的水平。此外,我们发现体育锻炼和RS能够差异性地调节组蛋白脱乙酰酶mRNA水平。最后,我们报告,在急性应激暴露前单次使用组蛋白脱乙酰酶抑制剂可防止总BDNF以及BDNF转录本1、2、3和6的下调,部分重现了体育锻炼的效果。总体而言,这些结果表明体育锻炼和应激能够通过可能不同的表观遗传机制差异性地调节BDNF转录本的表达。