Department of General Physiology and Biophysics, Faculty of Biology, University of Belgrade, Studentski trg 3, 11001, Belgrade, Serbia.
Department for Molecular biology and Endocrinology, Vinča Institute of Nuclear Sciences-National Institute of the Republic of Serbia, University of Belgrade, Belgrade, Serbia.
Neurochem Res. 2022 Jun;47(6):1637-1650. doi: 10.1007/s11064-022-03557-5. Epub 2022 Mar 23.
The present study demonstrates altered topographic distribution and enhanced neuronal expression of major adenosine-metabolizing enzymes, i.e. ecto-5'-nucleotidase (eN) and tissue non-specific alkaline phosphatase (TNAP), as well as adenosine receptor subtype A in the hippocampus and cortex of male rats from early to late adulthood (3, 6, 12 and 15 months old males). The significant effect of age was demonstrated for the increase in the activity and the protein expression of eN and TNAP. At 15-m, enzyme histochemistry demonstrated enhanced expression of eN in synapse-rich hippocampal and cortical layers, whereas the upsurge of TNAP was observed in the hippocampal and cortical neuropil, rather than in cells and layers where two enzymes mostly reside in 3-m old brain. Furthermore, a dichotomy in AR and AR expression was demonstrated in the cortex and hippocampus from early to late adulthood. Specifically, a decrease in AR and enhancement of AR expression were demonstrated by immunohistochemistry, the latter being almost exclusively localized in hippocampal pyramidal and cortical superficial cell layers. We did not observe any glial upregulation of AR, which was common for both advanced age and chronic neurodegeneration. Taken together, the results imply that the adaptative changes in adenosine signaling occurring in neuronal elements early in life may be responsible for the later prominent glial enhancement in AR-mediated adenosine signaling, and neuroinflammation and neurodegeneration, which are the hallmarks of both advanced age and age-associated neurodegenerative diseases.
本研究表明,雄性大鼠海马体和皮质中主要腺苷代谢酶(即外核苷酸酶 [eN] 和组织非特异性碱性磷酸酶 [TNAP])以及腺苷受体亚型 A 的拓扑分布发生改变,且神经元表达增强,这些改变发生在从早期到晚期成年(3、6、12 和 15 个月大的雄性)。年龄对 eN 和 TNAP 活性和蛋白表达的增加有显著影响。在 15 个月大时,酶组织化学显示 eN 在富含突触的海马体和皮质层中的表达增强,而 TNAP 的增加则发生在海马体和皮质神经胶质中,而不是在 3 个月大的大脑中两种酶主要存在的细胞和层中。此外,在从早期到晚期成年的皮质和海马体中,AR 和 AR 表达出现二分法。具体而言,免疫组织化学显示 AR 减少和 AR 表达增强,后者几乎仅定位于海马体锥体和皮质浅层细胞层。我们没有观察到任何胶质细胞 AR 的上调,这在衰老和慢性神经退行性变中很常见。总的来说,这些结果表明,生命早期神经元中发生的腺苷信号适应变化可能是导致后期胶质细胞中 AR 介导的腺苷信号增强、神经炎症和神经退行性变的原因,而这些正是衰老和与年龄相关的神经退行性疾病的特征。